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. 2026 Jan 28;6(1):e0004562. doi: 10.1371/journal.pgph.0004562

Pregnant women’s attitudes and intentions toward tuberculosis, malaria, group B streptococcus, and respiratory syncytial virus vaccines in pregnant: Findings from a cross-sectional study of pregnant women living in Brazil, Ghana, Kenya, and Pakistan

Rupali Limaye 1,2,*, Jessica Schue 1, Berhaun Fesshaye 1, Prachi Singh 1, Emily Miller 1, Renato Souza 3, Saleem Jessani 4, Marleen Temmerman 5, Caroline Dinam Badzi 6, Molly Sauer 1, Vanessa Brizuela 7, Ruth Karron 1
Editor: Giridhara Rathnaiah Babu8
PMCID: PMC12851439  PMID: 41604372

Abstract

There are numerous infections that can adversely impact a developing fetus, neonates, and pregnant women, and there is limited research related to how specific infections experienced during pregnancy can affect these populations. Tuberculosis (TB), malaria, Group B streptococcus (GBS) and respiratory syncytial virus (RSV) can cause negative outcomes to maternal and neonatal health. For TB and GBS, there are vaccines in various stages of clinical trial development, and malaria and RSV vaccines are available. This study aimed to examine pregnant women’s attitudes toward TB, malaria, GBS, and RSV vaccines in Brazil, Ghana, Kenya, and Pakistan. We administered a cross-sectional survey to pregnant women, recruiting women seeking care in primarily urban health facilities. We surveyed 1,603 pregnant women. Participants indicated that vaccine safety for the baby was the most important factor in their decision-making related to vaccine acceptance, followed by vaccine efficacy for the baby, and then vaccine safety for the mother. When asked why they would receive any of the four vaccines, participants indicated that protecting the baby was most important, followed by protecting self, and then stopping the spread of disease. Almost one-third of participants (30%) indicated that they would definitely intend to receive a GBS vaccine, followed by malaria (26%), RSV (25%), and TB (19%). Related to vaccine hesitancy, approximately 40% of our participants agreed that vaccines are unnatural, 38% agreed that the body should develop natural immunity, and 19% had delayed a recommended vaccine. Pregnant women are interested in receiving various vaccines while pregnant. As several new adult vaccines are on the horizon, understanding the attitudes of potential vaccine beneficiaries at higher risk for diseases is critical for informing clinical trial design and, in the long term, vaccine acceptance.

Introduction

Many infections pose unique risks to the developing fetus, neonate, and pregnant women [1]. Pregnant women face uncertainty not only during new infectious disease outbreaks, but also in relation to new vaccines in pregnancy. In addition, emerging infectious disease threats during pregnancy are often underrepresented in research, resulting in limited data and suboptimal preparedness planning [2].

One approach to reducing morbidity and mortality among these populations is maternal immunization. Vaccination during pregnancy offers not only protection to the pregnant women against the disease, but also passive immunity to an infant [3,4]. This is through an active process where maternal antibodies are transferred to a fetus through the placenta, offering protection to the infant as soon as it is born [3,4]. Further antibody transfer occurs during breastfeeding, providing additional protection to the infant when they are most vulnerable to infectious diseases [4]. There are several vaccines that are in various stages of clinical trial development, targeted to pathogens that cause substantial negative outcomes related to maternal and neonatal health and are thus priorities for use in pregnant women. These include maternal vaccines in development to target and Group B streptococcus (GBS) and malaria, recently approved maternal respiratory syncytial virus (RSV) vaccines, and future vaccines targeting tuberculosis (TB) [3]. These four diseases are of particular concern in low- and middle-income countries, where disease burden is disproportionately high and alternative prevention or treatment options are less commonly available or accessible.

TB is a significant cause of maternal mortality and morbidity globally [5,6]. Pregnant and postpartum women’s increased susceptibility to active TB and accelerated progression of disease may be due to the immunological changes that occur during pregnancy [7,8]. Active TB during pregnancy has also been linked to adverse outcomes for the baby including perinatal death, preterm birth, low birthweight, and fetal distress [6]. While epidemiologic data on TB during pregnancy are lacking due to inconsistent screening of pregnant women, a global burden study estimated that more than 200,000 active TB cases occurred during pregnancy in a single year [5,9]. Currently, the BCG vaccine is the only vaccine for TB prevention and offers protection for infants and young children, but this protection wanes in adolescence; BCG is not recommended in pregnancy [10,11]. Although multiple adult TB vaccines are in clinical development now, these vaccine trials do not currently include pregnant women as trial participants [11].

Malaria presents a significant global health challenge for pregnant women as well as their fetuses and newborns [12]. As with tuberculosis, pregnant women infected with malaria face increased morbidity and mortality compared to non-pregnant women [12,13]. Pregnant women infected with malaria may suffer from anemia, which in turn increases the risk of maternal mortality, whereas risks in-utero and to the infant include miscarriage, premature delivery, stillbirth, low birthweight, and cognitive-developmental delays [12,1416]. The World Health Organization approximates that in 2022, in countries where malaria transmission is considered to be moderate to high, more than one-third (36%) of pregnancies were exposed to malaria [17]. Each year, 125 million pregnant women are at risk of malarial infection [18]. In December 2024, the Sanaria PfSPZ malaria vaccine was the world’s first vaccine to be shown effective for malaria prevention before and during pregnancy [19]. An additional candidate product in development to prevent malaria during pregnancy is a VAR2CSA-based vaccine [20]. As of the writing of this paper, there are currently no approved vaccines for malaria prevention during pregnancy.

GBS is a bacterium that colonizes the vagina and rectum of pregnant people and is usually asymptomatic, but can occasionally cause severe disease in both the pregnant person and the neonate via passage in utero or during vaginal delivery [21]. GBS disease can cause maternal infection and sepsis, stillbirth, preterm birth, and early- and late-onset sepsis and meningitis in infants, which can be fatal [2123]. In 2020, GBS was estimated to have colonized approximately 20 million pregnant people, and caused approximately 400,000 cases of infant disease, 40,000 cases of maternal disease, and 46,000 stillbirths [24]. Intrapartum antibiotic prophylaxis (IAP) is currently the only available GBS disease prevention strategy, but it is programmatically complex to implement, only effective against early-onset GBS disease in infants, raises concerns about antimicrobial resistance, and is primarily an option in higher income settings only [25,26]. A GBS vaccine for pregnant women is prioritized for its potential to prevent both early and late-onset disease by providing transplacental antibody protection to newborns [27]. Two maternal GBS vaccines by Pfizer and MinervaX are currently in late-stage clinical development [26,27]. Pfizer’s GBS6 vaccine is a hexavalent conjugate vaccine targeting the six serotypes that produce 98% of disease [26]. MinervaX’s protein-only vaccine, GBS-NN/NN2, is intended to target all clinically significant isolates of GBS [3].

Limited data exist on RSV infection in pregnancy. A 2022 meta-analysis of five studies found a pooled prevalence for RSV of 0.2 per 100 pregnancies, but estimates varied widely across study countries [28]. RSV infection in pregnancy increases the risk of severe maternal disease, especially in those with preexisting lung conditions or coinfections [29]. RSV infection during pregnancy may also be associated with an increased risk of preterm delivery and/or low birth weight in the infant [28]. The impact of RSV on infants is well documented in global health literature; RSV is one of the primary causes of lower respiratory tract infection in children under the age of five, contributing to approximately 33 million infections and 101,400 deaths globally in 2019, with 95% of infections and 97% of deaths occurring in low- and middle-income countries [30]. Infants are at highest risk for severe RSV disease if they enter their first RSV season within the first six months of life [31]. Currently, two products are available to prevent severe RSV disease in infants: RSV monoclonal antibodies administered directly to infants, and an RSV prefusion F maternal vaccine administered to pregnant people that provides immunity to the infant for the first six months of life via placental antibody transfer [32]. As of late 2024, either or both products have been approved in more than 50 primarily high- and middle-income countries, but not in any low-income or lower-middle-income countries outside of India, despite their much greater RSV disease burden [32].

TB, malaria, GBS, and RSV cause negative maternal and neonatal health outcomes, and there are vaccines either available or in development for each of these diseases, including some specifically intended for use in pregnancy. As vaccination, not vaccines, save lives, the objective of this cross-sectional study was to understand and compare attitudes toward these potential vaccines among pregnant women receiving antenatal care in Brazil, Ghana, Kenya, and Pakistan. Individuals weigh multiple factors when deciding whether to be vaccinated and these attitudes and intentions are complex and both vaccine- and context-specific; vaccination in pregnancy presents even more complicated processes as pregnant women consider the benefits and risks to themselves and their babies [33,34]. The results of this study are intended to inform demand generation efforts for vaccine acceptance, understanding that such efforts should be context specific.

Methods

Ethics statement

This study was approved by the following institutional review boards: Johns Hopkins Bloomberg School of Public Health Institutional Review Board (00020864), University of Campinas/Unicamp Brazil (63968222.1.1001.5404), Jundiai University Institutional Review Board Brazil ((63968222.1.1001.5404), Ghana Health Service Ethics Review Committee (028/03/23), Aga Khan University Kenya (2023/ISERC-17(v2)), Pumwani Maternity Hospital (PMH/CEO/76/0785/2023), Aga Khan University Pakistan (2024-8633-30122), National Bioethics Committee for Research Pakistan (4–87/NBCR-1029/23/1087), and Ethics Research Committee World Health Organization (CERC.0193A, CERC.0193B, CERC.0193C), Ethics Review Committee Pan American Health Organization (PAHOERC.0633.01). Formal written consent was obtained for each participant.

Participants, study setting, and recruitment

This was part of a multi-country, cross-sectional, mixed-methods study using qualitative interviews and quantitative surveys to collect data on factors affecting COVID-19 vaccine decision making among pregnant and postpartum women in Brazil, Ghana, Kenya, and Pakistan. The study protocol and instruments are available online [35]. This analysis includes questions about future maternal vaccines from the quantitative surveys and focused on vaccine intentions related to these diseases in pregnancy. Study sites were located across the four countries, with health facilities included in the study serving a variety of different patient populations. In total, data were collected in nine facilities across the four countries. In Brazil, the research was carried out in two maternity hospitals in the urban São Paulo region: CAISM/Unicamp Hospital in Campinas and Hospital Universitario de Jundiaí in Jundiaí. Data were collected between August 21, 2023 and December 4, 2023. In Ghana, three hospitals in the Greater Accra Region were included: Ga West Hospital, Tema General Hospital, and Shai-Osuduko Hospital. Data were collected between October 25,2023 and November 10, 2023. In Kenya, the study was conducted at two antenatal clinics based in referral hospitals of Nairobi: Aga Khan University Hospital and Pumwani Maternity Hospital. Data were collected between October 13, 2023 and March 8, 2024. In Pakistan, two hospitals in Karachi were involved: Aga Khan Hospital for Women and Children, Kharadar and the Jinnah Postgraduate Medical Center OBGYN Department. Data were collected between February 26, 2024 and May 25, 2024.

We aimed to survey 400 pregnant individuals in each country, for a total of 1,600 surveys. The sample size was determined with 80% power to find differences in proportions of respondents with a positive or negative attitude toward vaccines in pregnancy between two groups with a 5% margin of error. We sought to sample approximately equal numbers by pregnancy trimester. Surveys were administered to pregnant individuals seeking maternity care. Recruitment strategy varied by country, with sites recruiting from waiting areas in clinics using consecutive sampling. In Brazil, every nth person in the waiting area was approached, with n varying based on patient volume per site. Ghana, Kenya, and Pakistan used a consecutive sampling approach to recruit from either waiting or reception areas.

Data collection

Trained study staff approached women and read a recruitment script to assess eligibility: 1) study interest, 2) age 18 or older (or an emancipated minor - in Brazil only), 3) fluency in the local language or English, and 4) having heard of the COVID-19 vaccine. Eligible participants interested in joining the study went through a written informed consent process and were provided with written participation information sheets. Study staff paused any study activities if the participant was called to see a provider and restarted after the visit was complete. Ghana, Kenya, and Pakistan provided transportation remuneration or a food box to participants after administration of the survey; Brazil did not provide any remuneration.

The survey instrument was developed to identify attitudinal, behavioral, intentional, and psychosocial correlates of vaccine behavior. The instrument was developed by using a comprehensive and iterative process that included a literature review and review of relevant instruments. The instrument was then reviewed by country teams, pre-tested, and then finalized and aligned with the local contexts. Each country’s data collection team was trained separately by members of the team from Johns Hopkins Bloomberg School of Public Health through a three-day training session. Training sessions included information and practice related to human subject research ethics, quantitative survey best practices, and study instrument practice.

Data collection included a single questionnaire, with Brazil and Kenya using paper-based data collection and Ghana and Pakistan using tablet-based data collection using either the REDCap Mobile Application or REDCap’s web-based data entry interface [36,37]. All study data were managed and stored using REDCap electronic data capture tools hosted at Johns Hopkins Bloomberg School of Public Health. Data collection was done in Brazilian Portuguese in Brazil; Ga, Twi, or English in Ghana; Kiswahili or English in Kenya; and Urdu in Pakistan. The survey took approximately 30–60 minutes to complete.

Measures

The full survey is publicly available [38]. The sections used in this analysis are described below.

Sociodemographic characteristics (5 items).

We asked participants to indicate their age (18–24, 25–34, 35–49, 50+), marital status (single/never married, married or cohabitating with partner, divorced/widowed/separated), trimester (first trimester 1–12 weeks, second trimester 13–26 weeks, third trimester 27 weeks or more), how many children under the age of 18 they had (none, one, two, three, four or more), and level of education (no formal schooling, less than primary school, primary school completed, secondary/high school completed, college/university completed, post graduate degree completed).

Decision-making factors related to future maternal vaccines (2 items).

We asked women to identify 3 factors that were most and least important to them related to future maternal vaccines: “We are interested in understanding what would be most important to you in your decision to receive any new vaccines for pregnant women (for example vaccines against tuberculosis, malaria, Streptococcus B, respiratory syncytial virus) whenever they become available. Which of the following factors are MOST IMPORTANT in informing your decision to take new vaccines. You can choose up to three factors that are most important to you” (how well the vaccine works in protecting me, how well the vaccine works in protecting my baby, my doctor’s recommendation about the vaccine, my family’s recommendation about the vaccine, safety of the vaccine for me, safety of the vaccine for my baby). We also asked women to rank in order the 3 least important decision-making factors out of six factors: “Which of the following factors are LEAST IMPORTANT in informing your decision to take new vaccines. You can choose up to three factors that are least important to you” (how well the vaccine works in protecting me, how well the vaccine works in protecting my baby, my doctor’s recommendation about the vaccine, my family’s recommendation about the vaccine, safety of the vaccine for me, safety of the vaccine for my baby).

Future maternal vaccine intentions (4 items).

We asked about future maternal vaccine intentions related to tuberculosis, malaria, Group B streptococcus, and respiratory syncytial virus using a 3-point scale. For each vaccine, we asked women to rate their intention to receive the vaccine: “We would like to understand your interest in receiving specific vaccines that are currently being developed and may become available for pregnant people in the future. For each of the following vaccines, if the vaccine were to become available in your country in the future and your doctor recommended it during pregnancy, what would be your intention to receive the vaccine?” (I would definitely intend to receive it, maybe I would receive it, I would have no intentions of receiving it).

Vaccine hesitancy (3 items).

We asked 3 questions to measure vaccine hesitancy: 2 questions related to COVID-19 vaccines during pregnancy, and one related to past vaccination behavior, and these were COVID-19 specific as this analysis was conducted within the context of a larger study that aimed to understand COVID-19 vaccine acceptance during pregnancy. We asked women to rate their level of agreement with the following statements on a 4-point Likert scale: “I do not want to put the COVID-19 vaccine into my body when I am pregnant because I think it is unnatural” and “Vaccines improve your body’s ability to fight off diseases; this is known as immunity. I believe it is better for my body to develop immunity by getting sick than by getting the COVID-19 vaccine.” (strongly agree, agree, disagree, strongly disagree). Finally, we asked about past vaccination behavior: “Have you ever delayed getting a recommended vaccine or decided not to get a recommended vaccine for reasons other than illness or allergy?” (yes, no, don’t know).

Family influence related to future maternal vaccines (1 item).

We asked women their level of agreement using a 4-point Likert scale with the following statement: “My family would encourage me to get any vaccine that was recommended during my pregnancy” (strongly agree, agree, disagree, strongly disagree).

Priority maternal vaccine and decision-making (2 items).

After providing brief descriptions of the diseases the vaccines could potentially prevent, we asked women which of the four potential future maternal vaccines to select the one that they were most interested in: “If it were to become available in your country, which one of the vaccines (tuberculosis, malaria, Group B streptococcus, respiratory syncytial virus) would you be most interested in receiving during pregnancy?” (tuberculosis vaccine, malaria vaccine, Group B streptococcus vaccine (against blood infections and meningitis in babies), respiratory syncytial virus vaccine (against wheezing and pneumonia in children). We asked them to rank in order the reasons that they would want that particular vaccine: “For the vaccine that you chose in the last question, we have listed multiple reasons why people may want to get that vaccine. Please rank these reasons in order, with 1 being the most important aspect to you for getting the vaccine, to 5 being the least relevant factor in your decision to get the vaccine.” (I want to protect myself against the disease, I want to protect my baby against the disease, I want to reduce my risk of spreading the disease to others (to protect my family, friends, and others against the disease), my doctor would want me to get the vaccine, my partner and/or my family would want me to get the vaccine).

Data analysis

After reviewing the data for completeness, we followed a standard protocol for data cleaning, including managing missing data. We calculated frequencies and developed histograms for each variable. Descriptive statistics of sociodemographic variables were calculated for individual countries. Chi-square tests were used for all comparisons between countries. For the variables using 4-point Likert scales, the most extreme responses (strongly agree or strongly disagree) were the least frequent therefore we collapsed these into two categories: agree (strongly agree and agree) and disagree (strongly disagree and disagree). Responses to ranking questions were summarized by the mean rank for each reason selected overall and by country, and the percent of respondents that selected each reason as their most important reason. Data analysis was done in Stata (v18, College Station, TX) and R Statistical Software (v4.4.2, R Core Team 2024).

Results

There were 1,603 women that participated in our study. Most of the participants were aged 25–34 (55.2%), married or cohabitating (82.6%), had no children under the age of 18 (39.9%), and had completed secondary/high school (47.8%). See Table 1 for sociodemographic characteristics of the study sample.

Table 1. Sociodemographic characteristics overall and by country.

Overall (N = 1603) Brazil (N = 402) Ghana (N = 401) Kenya (N = 400) Pakistan (N = 400)
Age, n(%)
 < 18 and emancipated 6 (0.4) 6 (1.5) 0 (0.0) 0 (0.0) 0 (0.0)
 18-24 402 (25.1) 109 (27.1) 80 (20.0) 61 (15.2) 152 (38.0)
 25-34 885 (55.2) 198 (49.3) 224 (55.9) 249 (62.3) 214 (53.5)
 35-49 310 (19.3) 89 (22.1) 97 (24.2) 90 (22.5) 34 (8.5)
Marital status, n(%)
 Single (never married) 257 (16.0) 125 (31.1) 91 (22.7) 41 (10.2) 0 (0.0)
 Married or cohabitating 1324 (82.6) 263 (65.4) 303 (75.6) 358 (89.5) 400 (100.0)
 Divorced, separated, or widowed 22 (1.4) 14 (3.5) 7 (1.7) 1 (0.2) 0 (0.0)
Pregnancy Trimester, n(%)
 First trimester (1–12 weeks) 446 (27.8) 133 (33.1) 49 (12.2) 131 (32.8) 133 (33.2)
 Second trimester (13–26 weeks) 572 (35.7) 135 (33.6) 170 (42.4) 134 (33.5) 133 (33.2)
 Third trimester (from 27 weeks) 585 (36.5) 134 (33.3) 182 (45.4) 135 (33.8) 134 (33.5)
Living children under 18 years of age, n(%)
 None 639 (39.9) 160 (39.8) 151 (37.7) 165 (41.2) 163 (40.8)
 One 472 (29.4) 135 (33.6) 102 (25.4) 132 (33.0) 103 (25.8)
 Two 313 (19.5) 70 (17.4) 87 (21.7) 77 (19.2) 79 (19.8)
 Three 118 (7.4) 21 (5.2) 41 (10.2) 20 (5.0) 36 (9.0)
 Four or more 61 (3.8) 16 (4.0) 20 (5.0) 6 (1.5) 19 (4.8)
Education level, n(%)
 No formal schooling 18 (1.1) 0 (0.0) 3 (0.7) 0 (0.0) 15 (3.8)
 Less than primary school 85 (5.3) 31 (7.7) 12 (3.0) 9 (2.2) 33 (8.2)
 Primary school completed 190 (11.9) 65 (16.2) 30 (7.5) 37 (9.2) 58 (14.5)
 JHS/SHS school completed 767 (47.8) 257 (63.9) 245 (61.1) 83 (20.8) 182 (45.5)
 College/University completed 441 (27.5) 44 (10.9) 90 (22.4) 208 (52.0) 99 (24.8)
 Post-graduate degree 97 (6.1)* 5 (1.2)* 16 (4.0) 63 (15.8) 13 (3.2)

*n=5 missing.

We asked participants to choose which factors (up to three factors) were most important related to informing their decision-making for vaccines in pregnancy. Overall, the most frequently selected factor was vaccine safety for the baby (65.3%) followed closely by efficacy for the baby (57.6%), while the least selected reason related to family recommendations (21.5%). For the most part, country specific data followed similar trends with a few exceptions (Fig 1). In Kenya, vaccine safety for the mother was chosen most frequently, while in Ghana, vaccine efficacy for the mother was chosen most frequently. While a family recommendation was the lowest selected factor overall, Pakistan had a greater number of participants selecting family and doctor recommendation compared to the other countries.

Fig 1. Priority factors for informing decision-making for future maternal vaccines.

Fig 1

We then examined vaccine intention for each of the four vaccines by country. To illustrate the range of vaccine intentions, Fig 2 shows future maternal vaccine intentions per vaccine by country, denoting the number of participants by country that would intend to definitely receive the vaccine, maybe receive the vaccine, and would have no intentions in receiving the vaccine during pregnancy. There were some interesting country differences: the majority of participants in Pakistan and Brazil indicated that they would definitely intend to receive all four vaccines during pregnancy. In Ghana, there was a higher proportion of participants that indicated they would maybe receive the TB, RSV, and GBS vaccine, compared to other countries. The largest number of participants not intending to receive the TB vaccine was in Kenya. By country, the majority of participants in Brazil definitely intended to receive a GBS vaccine, followed closely by an RSV vaccine; the majority of Ghanaian participants definitely intended to receive a malaria vaccine; in Kenya, the majority of participants definitely intended to receive an RSV vaccine, followed closely by a GBS vaccine; and in Pakistan, the majority of participants definitely intended to receive an RSV vaccine, followed closely by a GBS vaccine. Overall, across all four countries and vaccines, all had the greatest number of participants in the definitely yes and maybe categories as compared to the no category.

Fig 2. Intentions to receive vaccines during pregnancy across countries.

Fig 2

We examined vaccine attitudes broadly among our participants overall and by country (Table 2). We asked three questions related to vaccine hesitancy: 40.1% of our participants agreed that vaccines are unnatural, 37.5% agreed that the body should develop natural immunity, and 19.2% had delayed a recommended vaccine. There were some notable differences by country. Participants in Brazil were less likely to believe that the body should develop natural immunity compared to the other countries (12.9% vs 36.4% in Ghana, 48.8% in Kenya, and 52.0% in Pakistan). Very few participants in Pakistan indicated that they had ever delayed a recommended vaccine (2.0%). Related to family influence, overall, approximately 82% of participants agreed that their family would encourage them to get a vaccine recommended during pregnancy, ranging from 73% in Ghana to 92% in Pakistan. Related to future vaccine intentions, the proportion of participants who indicated that they would definitely intend to receive TB, malaria, GBS, or RSV vaccines in pregnancy was generally high (ranging from 71.4% to 81.3% across the various vaccines). There were differences at the country level, with participants in Ghana had the lowest intentions to definitely receive any of the four vaccines except for the malaria vaccine, while participants in Brazil had the lowest intentions to definitely receive the malaria vaccine across the four vaccines in pregnancy.

Table 2. Attitudes toward vaccines during pregnancy overall and by country.

Overall (N = 1603) Brazil (N = 402) Ghana (N = 401) Kenya (N = 400) Pakistan (N = 400) p-value*
Vaccine hesitancy: agree or yes, n(%)
 The vaccine is unnatural 643 (40.1) 107 (26.6) 156 (38.9) 153 (38.2) 227 (56.8) <0.001
 Immunity is better than a vaccine 601 (37.5) 52 (12.9) 146 (36.4) 195 (48.8) 208 (52.0) <0.001
 Delayed vaccination 307 (19.2) 135 (33.6) 65 (16.2) 99 (24.8) 8 (2.0) <0.001
Family influence: agree, n(%)
 My family would encourage me to get any vaccine 1315 (82.0) 339 (84.3) 291 (72.6) 319 (79.8) 366 (91.5) <0.001
Future maternal vaccines intentions: definitely intend to receive, n(%)
 Tuberculosis vaccine 1144 (71.4) 313 (77.9) 263 (65.6) 246 (61.5) 322 (80.5) <0.001
 Malaria vaccine 1285 (80.2) 315 (78.4) 358 (89.3) 286 (71.5) 326 (81.5) <0.001
 GBS vaccine 1297 (80.9) 367 (91.3) 272 (67.8) 322 (80.5) 336 (84.0) <0.001
 RSV vaccine 1304 (81.3) 362 (90.0) 271 (67.6) 325 (81.2) 346 (86.5) <0.001
Priority maternal vaccine: top choice, n(%)
 Tuberculosis vaccine 298 (18.6) 50 (12.4) 58 (14.5) 73 (18.2) 117 (29.2)
 Malaria vaccine 413 (25.8) 15 (3.7) 222 (55.4) 104 (26.0) 72 (18.0)
 GBS vaccine 483 (30.1) 205 (51.0) 64 (16.0) 104 (26.0) 110 (27.5)
 RSV vaccine 408 (25.5) 131 (32.6) 57 (14.2) 119 (29.8) 101 (25.2) <0.001

*p-values are from chi-squared tests comparing responses between countries.

GBS: Group B streptococcus, RSV: respiratory syncytial virus.

For all the variables using 4-point Likert scales, response options were collapsed into two categories: agree (strongly agree and agree) and disagree (strongly disagree and disagree).

To understand the salience of decision-making factors related to vaccines in pregnancy, we asked women select the vaccine they were most interested in receiving during pregnancy: TB, malaria, GBS, or RSV. The proportion of overall participants that selected each future vaccine in pregnancy is summarized in Fig 3. Almost one-third of our overall sample (30.1%) prioritized receiving a GBS vaccine, followed by malaria (25.8%), RSV (25.5%), and TB (18.6%) vaccine in pregnancy (Fig 3). At the country-level, the biggest proportion of women in Brazil (51.0%) and Pakistan (27.5%) chose GBS as their priority vaccine. More than half women in Ghana (55.4%) prioritized the malaria vaccine, while in Kenya 29.8% of women selected the RSV vaccine as their priority vaccine to receive in pregnancy.

Fig 3. Priority future vaccine for use in pregnancy.

Fig 3

For the vaccine a person chose as their priority to receive during pregnancy, we asked participants to then rank factors in order of importance for receiving their chosen priority vaccine. We constructed a heatmap to illustrate their rankings (Fig 4). Overall, participants indicated that protecting the baby was most important (50.2%), followed by protecting themselves (36.4%), followed by stopping the spread of disease (5.8%). By country, these were also the first and second factors chosen across Brazil, Kenya, and Pakistan. In Ghana, the most important factor was protecting themselves, followed by protecting the baby, and then stopping the spread of the disease. In Pakistan, the most important factors were protecting the baby, followed by protecting themselves, and in third place a doctor’s recommendation.

Fig 4. Most important factors for taking their chosen priority vaccine.

Fig 4

Discussion

Our study indicated that vaccine safety for the baby and protecting the baby were the most important factors in vaccine acceptance in pregnancy, followed by self-protection and stopping the spread of disease. Pregnant women are interested in receiving various vaccines during pregnancy, which is important as several new adult vaccines are on the horizon, some of which are designed specifically for pregnancy and others that can be used in pregnancy. Understanding the attitudes of potential vaccine beneficiaries at higher risk for diseases, such as pregnant women, is critical for informing clinical trial design and, in the long term, vaccine acceptance.

Our results align with the broader literature in highlighting high vaccine acceptance during pregnancy, particularly for vaccines developed specifically for use in pregnancy. This includes GBS, where other studies found that acceptance was driven by perceived benefits and low barriers [39]. The high interest in GBS vaccines from participants from Brazil may stem from broader concern about meningitis and sepsis (“blood infections”) in newborns; GBS screening and IAP are inconsistent in Brazil, as in many LMICs [40,41], but recent studies have indicated a relatively high prevalence and severity of GBS in the country and growing concern about antibiotic resistance [23,4247]. Together, these may have helped drive the relatively higher interest in GBS vaccines in Brazil compared to other vaccines and study countries. With GBS vaccines on the horizon, further research could help prepare Brazilian communities and health workers to leverage this demand and improve GBS prevention.

Similarly, intention to receive the RSV vaccine is consistent with high acceptance rates reported in Canada and the United States, both over 50%, where the perception of RSV as a serious illness strongly influenced vaccination intentions [4850]. However, the study also revealed notable country-level differences in vaccine priorities, such as Kenyan participants favoring the RSV vaccine and Ghanaian participants prioritizing the malaria vaccine. These variations suggest the importance of context-specific factors; local disease burden and healthcare contexts significantly shape vaccine intentions.

There was equally as strong support for adult vaccines that can be used in pregnancy. Strong interest in TB vaccination in pregnancy was the most common responses across all four countries. This aligns with reports among women in Amhara, Ethiopia, who expressed strong acceptance due to perceived benefits for child protection and societal health [51]. Furthermore, research on TB vaccine acceptance in pregnancy is currently sparse and our findings provide new insights. There was also strong interest in receiving a malaria vaccine in pregnancy, with notable differences in priority by countries with different disease burdens. The research community has agreed that including pregnant women in malaria vaccine efficacy trials should be done, which will provide the needed safety data to help decision making [52]. Malaria vaccines intended specifically for use in pregnancy are also possible, but early in clinical development [53,54].

Our study highlights the important role of vaccine safety and efficacy in shaping pregnant women’s decisions regarding immunization. Our finding of the importance of vaccine safety and efficacy for the baby followed by vaccine safety for the mother aligns with prior studies indicating that pregnant women are more likely to accept vaccines when they have confidence in their safety and perceive a benefit to their babies [5557].These results underscore the need for pregnancy-specific safety data, which can only be generated through the active inclusion of pregnant women in clinical trials. Although trials are enrolling pregnant women, their participation is variable which can be improved by incorporating their concerns and priorities in trial design to generate robust evidence in this population [5861]. Previous research has similarly found that maternal vaccine acceptance is influenced by vaccine safety, vaccine effectiveness, lack of vaccine knowledge, mistrust of vaccines, perceived disease severity, and lack of recommendation to receive vaccines [62]. This suggests that pregnant women may perceive varying levels of risk and benefit associated with different diseases, further emphasizing the need for targeted educational interventions and communication regarding disease severity and vaccine effectiveness.

Furthermore, our study identified a significant level of vaccine hesitancy, defined as agreeing that vaccines are unnatural, believing that natural immunity is preferable, and ever having previously delayed a recommended vaccine. These attitudes, while consistent with region-specific trends of vaccine hesitancy, were less prevalent in Pakistan, where family encouragement for vaccination was highest. These concerns reinforce the ethical argument that excluding pregnant women from trials results in greater harm, as it deprives them of reliable safety data and contributes to uncertainty [63].

Vaccine uptake is multi-factorial. We examined factors related to intentions to get future recommended vaccines during pregnancy which are important when planning new vaccine introductions [64]. Given that pregnant women report that safety and protection for themselves and their newborns are the primary salient factors in the decision-making process for both existing and new vaccines, future research should focus on developing appropriate and culturally relevant messaging to ensure proper dissemination and uptake. Notable, also, is the role of healthcare providers in immunization among pregnant and post-pregnant women. Further research should focus on understanding their perceptions and motivations in providing recommendations among pregnant and recently pregnant women. Similarly important, is to look at different intersectional factors that might influence maternal immunization. This would include gathering perspectives of women living in rural areas, women with different abilities, indigenous women, and women of different ethnic and racial backgrounds, as well as any intersectional factors [65]. Overall, our study underscores the importance of contextual factors in shaping vaccine intentions, complementing previous literature while highlighting unique regional variations.

This study has limitations. Participants were recruited in health facilities while seeking antenatal care, which limited our sample selection to pregnant women seeking preventative care. Access and scale of ANC services in each setting likely influenced the study sample. Clinics were chosen to represent different socioeconomic groups of participants but are likely not representative. Administering the surveys in health facilities may have led to social desirability bias. Data are self-reported and are subject to recall bias. This analysis was done as part of a larger study that focused on COVID-19 vaccination for pregnant women, and as such, constructs were focused on attitudes toward COVID-19 vaccines. We did not provide detail on the four future vaccines or diseases to survey respondents, beyond a simple description of RSV and GBS disease; without such background, limited respondent knowledge of these four diseases in pregnancy and neonates may have influenced responses. Despite these limitations, our study has several strengths. This is one of the first studies to examine pregnant women’s attitudes toward future vaccines across several different countries, which is critical for new vaccine sensitization, delivery, and uptake.

Participants’ willingness to receive a variety of vaccines while pregnant is promising and indicates the potential for high uptake. Several new adult vaccines are on the horizon, some targeted specifically for use in pregnancy. Understanding the attitudes of potential vaccine beneficiaries at higher risk for diseases that vaccines may be able to prevent can help inform clinical trial study design, and in the long-term, demand generation strategies for successful uptake.

Data Availability

There are ethical and legal restrictions which prevent the public sharing of minimal data for this study, because the data contain potentially identifiable participant information. Data for this study are available upon request via email from IRB contacts at the University of Campinas (cep@unicamp.br), Ghana Health Service (ethics.research@ghs.gov.gh), KEMRI (director@kemri.org), NBC Pakistan (nbcpakistan@nih.org.pk), and JHU IRB (BSPH.irboffice@jhu.edu) for researchers who meet the criteria for access to confidential data.

Funding Statement

This study was funded by the Gates Foundation (grant INV-016977 to R.J.L/R.A.K) at the Johns Hopkins Bloomberg School of Public Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.Kourtis AP, Read JS, Jamieson DJ. Pregnancy and Infection. N Engl J Med [Internet]. 2014 Jun 5 [cited 2025 Jan 15];370(23):2211–8. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459512/ [DOI] [PMC free article] [PubMed]
  • 2.Meaney-Delman D, Carroll S, Polen K, Jatlaoui TC, Meyer S, Oliver S. Planning for the future of maternal immunization: Building on lessons learned from the COVID-19 pandemic. Vaccine. 2024;42(Suppl 3):125644. doi: 10.1016/j.vaccine.2024.125644 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Adams RM, Gonik B. The Evolving Maternal Vaccine Platform. Reprod Med [Internet]. 2024 Aug 7 [cited 2025 Jan 31];5(3):154–71. Available from: https://www.mdpi.com/2673-3897/5/3/14
  • 4.Chu HY, Englund JA. Maternal immunization. Clin Infect Dis. 2014;59(4):560–8. doi: 10.1093/cid/ciu327 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Mathad JS, Yadav S, Vaidyanathan A, Gupta A, LaCourse SM. Tuberculosis Infection in Pregnant People: Current Practices and Research Priorities. Pathogens [Internet]. 2022 Dec [cited 2025 Jan 8];11(12):1481. Available from: https://www.mdpi.com/2076-0817/11/12/1481 [DOI] [PMC free article] [PubMed]
  • 6.Sobhy S, Babiker Z, Zamora J, Khan KS, Kunst H. Maternal and perinatal mortality and morbidity associated with tuberculosis during pregnancy and the postpartum period: a systematic review and meta-analysis. BJOG. 2017;124(5):727–33. doi: 10.1111/1471-0528.14408 [DOI] [PubMed] [Google Scholar]
  • 7.Bates BR, Villegas-Botero A, Costales JA, Moncayo AL, Tami A, Carvajal A, et al. COVID-19 Vaccine Hesitancy in Three Latin American Countries: Reasons Given for Not Becoming Vaccinated in Colombia, Ecuador, and Venezuela. Health Commun. 2022;37(12):1465–75. doi: 10.1080/10410236.2022.2035943 [DOI] [PubMed] [Google Scholar]
  • 8.Orazulike N, Sharma JB, Sharma S, Umeora OUJ. Tuberculosis (TB) in pregnancy – A review. European Journal of Obstetrics & Gynecology and Reproductive Biology [Internet]. 2021 Apr 1 [cited 2025 Jan 8];259:167–77. Available from: https://www.sciencedirect.com/science/article/pii/S0301211521000956 [DOI] [PubMed]
  • 9.Sugarman J, Colvin C, Moran AC, Oxlade O. Tuberculosis in pregnancy: an estimate of the global burden of disease. Lancet Glob Health. 2014;2(12):e710-6. doi: 10.1016/S2214-109X(14)70330-4 [DOI] [PubMed] [Google Scholar]
  • 10.World Health Organization. Global Tuberculosis Report 2024 [Internet]. 2024 [cited 2025 Jan 8]. Available from: https://www.who.int/teams/global-tuberculosis-programme/tb-reports
  • 11.Zhuang L, Ye Z, Li L, Yang L, Gong W. Next-Generation TB Vaccines: Progress, Challenges, and Prospects. Vaccines (Basel) [Internet]. 2023 Jul 31 [cited 2025 Jan 8];11(8):1304. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457792/ [DOI] [PMC free article] [PubMed]
  • 12.Reddy V, Weiss DJ, Rozier J, Ter Kuile FO, Dellicour S. Global estimates of the number of pregnancies at risk of malaria from 2007 to 2020: a demographic study. Lancet Glob Health. 2023;11(1):e40–7. doi: 10.1016/S2214-109X(22)00431-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Desai M, Hill J, Fernandes S, Walker P, Pell C, Gutman J, et al. Prevention of malaria in pregnancy. The Lancet Infectious Diseases [Internet]. 2018 Apr 1 [cited 2025 Jan 9];18(4):e119–32. Available from: https://www.sciencedirect.com/science/article/pii/S1473309918300641
  • 14.Lawford HLS, Nuamah MA, Liley HG, Griffin A, Lekpor CE, Botchway F, et al. Associations between malaria in pregnancy and neonatal neurological outcomes. International Journal of Infectious Diseases [Internet]. 2021. Nov 1 [cited 2025 Jan 9];112:144–51. Available from: https://www.sciencedirect.com/science/article/pii/S1201971221005932 [DOI] [PubMed] [Google Scholar]
  • 15.Saito M, Briand V, Min AM, McGready R. Deleterious effects of malaria in pregnancy on the developing fetus: a review on prevention and treatment with antimalarial drugs. The Lancet Child & Adolescent Health [Internet]. 2020 Oct 1 [cited 2025 Jan 9];4(10):761–74. Available from: https://www.sciencedirect.com/science/article/pii/S2352464220300997 [DOI] [PubMed]
  • 16.Satapathy P, Khatib MN, Gaidhane S, Zahiruddin QS, Sharma RK, Rustagi S, et al. Adverse pregnancy outcomes in maternal malarial infection: A systematic review and meta-analysis. New Microbes and New Infections [Internet]. 2024 Dec 1 [cited 2025 Jan 9];62:101474. Available from: https://www.sciencedirect.com/science/article/pii/S2052297524002580 [DOI] [PMC free article] [PubMed]
  • 17.World malaria report 2023 [Internet]. 2023 [cited 2025 Jan 9]. Available from: https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2023
  • 18.Das JK, Lakhani S, Rahman AR, Siddiqui F, Padhani ZA, Rashid Z, et al. Malaria in pregnancy: Meta-analyses of prevalence and associated complications. Epidemiology & Infection [Internet]. 2024 Jan [cited 2025 Jan 9];152:e39. Available from: https://www.cambridge.org/core/journals/epidemiology-and-infection/article/malaria-in-pregnancy-metaanalyses-of-prevalence-and-associated-complications/80F761848A87543B9B0C032644AC684D [DOI] [PMC free article] [PubMed]
  • 19.Diawara H, Healy SA, Mwakingwe-Omari A, Issiaka D, Diallo A, Traore S, et al. Safety and efficacy of PfSPZ Vaccine against malaria in healthy adults and women anticipating pregnancy in Mali: two randomised, double-blind, placebo-controlled, phase 1 and 2 trials. Lancet Infect Dis. 2024;24(12):1366–82. doi: 10.1016/S1473-3099(24)00360-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Fried M, Duffy PE. Designing a VAR2CSA-based vaccine to prevent placental malaria. Vaccine [Internet]. 2015 Dec 22 [cited 2025 Jan 9];33(52):7483–8. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077158/ [DOI] [PMC free article] [PubMed]
  • 21.Armistead B, Oler E, Adams Waldorf K, Rajagopal L. The Double Life of Group B Streptococcus: Asymptomatic Colonizer and Potent Pathogen. Journal of Molecular Biology [Internet]. 2019 Jul [cited 2025 Jan 13];431(16):2914–31. Available from: https://linkinghub.elsevier.com/retrieve/pii/S00222 [DOI] [PMC free article] [PubMed]
  • 22.Russell NJ, Seale AC, O’Driscoll M, O’Sullivan C, Bianchi-Jassir F, Gonzalez-Guarin J, et al. Maternal Colonization With Group B Streptococcus and Serotype Distribution Worldwide: Systematic Review and Meta-analyses. Clinical Infectious Diseases [Internet]. 2017 Nov 6 [cited 2025 Jan 13];65(suppl_2):S100–11. Available from: https://academic.oup.com/cid/article/65/suppl_2/S100/4589589 [DOI] [PMC free article] [PubMed]
  • 23.Tavares T, Pinho L, Bonifácio Andrade E. Group B streptococcal neonatal meningitis. Clin Microbiol Rev. 2022;35(2):e0007921. doi: 10.1128/CMR.00079-21 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Gonçalves BP, Procter SR, Paul P, Chandna J, Lewin A, Seedat F, et al. Group B streptococcus infection during pregnancy and infancy: estimates of regional and global burden. The Lancet Global Health [Internet]. 2022 Jun [cited 2025 Jan 13];10(6):e807–19. Available from: https://linkinghub.elsevier.com/retrieve/pii/S2214109X22000936 [DOI] [PMC free article] [PubMed]
  • 25.Le Doare K, O’Driscoll M, Turner K, Seedat F, Russell NJ, Seale AC, et al. Intrapartum Antibiotic Chemoprophylaxis Policies for the Prevention of Group B Streptococcal Disease Worldwide: Systematic Review. Clinical Infectious Diseases [Internet]. 2017 Nov 6 [cited 2025 Jan 13];65(suppl_2):S143–51. Available from: https://academic.oup.com/cid/article/65/suppl_2/S143/4589585 [DOI] [PMC free article] [PubMed]
  • 26.Steer PJ, Russell AB, Kochhar S, Cox P, Plumb J, Gopal Rao G. Group B streptococcal disease in the mother and newborn—A review. European Journal of Obstetrics & Gynecology and Reproductive Biology [Internet]. 2020 Sep [cited 2025 Jan 13];252:526–33. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0301211520303912 [DOI] [PMC free article] [PubMed]
  • 27.Kobayashi M, Schrag SJ, Alderson MR, Madhi SA, Baker CJ, Sobanjo-Ter Meulen A, et al. WHO consultation on group B Streptococcus vaccine development: report from a meeting held on 27-28 April 2016. Vaccine. 2019;37(50):7307–14. doi: 10.1016/j.vaccine.2019.09.045 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Riccò M, Ferraro P, Corrado S, Zaniboni A, Satta E, Ranzieri S. Respiratory Syncytial Virus in Pregnant Women: Systematic Review and Meta-Analysis. Women [Internet]. 2022 Jun 10 [cited 2025 Jan 13];2(2):147–60. Available from: https://www.mdpi.com/2673-4184/2/2/16
  • 29.Kachikis AB, Cho H, Englund JA. Respiratory Syncytial Virus—An Update for Prenatal and Primary Health Providers. Obstetrics and Gynecology Clinics of North America [Internet]. 2023 Jun [cited 2025 Jan 13];50(2):421–37. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0889854523000451 [DOI] [PubMed]
  • 30.Li Y, Wang X, Blau DM, Caballero MT, Feikin DR, Gill CJ, et al. Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. Lancet. 2022;399(10340):2047–64. doi: 10.1016/S0140-6736(22)00478-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Esposito S, Abu Raya B, Baraldi E, Flanagan K, Martinon Torres F, Tsolia M, et al. RSV Prevention in All Infants: Which Is the Most Preferable Strategy? Front Immunol [Internet]. 2022 Apr 28 [cited 2025 Jan 13];13:880368. Available from: https://www.frontiersin.org/articles/10.3389/fimmu.2022.880368/full [DOI] [PMC free article] [PubMed]
  • 32.Pecenka C, Sparrow E, Feikin DR, Srikantiah P, Darko DM, Karikari-Boateng E, et al. Respiratory syncytial virus vaccination and immunoprophylaxis: realising the potential for protection of young children. The Lancet [Internet]. 2024 Sep 21 [cited 2025 Jan 9];404(10458):1157–70. Available from: https://www.proquest.com/docview/3106957807/abstract/219B7A7D26914C31PQ/1 [DOI] [PubMed]
  • 33.Kilich E, Dada S, Francis MR, Tazare J, Chico RM, Paterson P, et al. Factors that influence vaccination decision-making among pregnant women: A systematic review and meta-analysis. PLoS One. 2020;15(7):e0234827. doi: 10.1371/journal.pone.0234827 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Smith SE, Sivertsen N, Lines L, De Bellis A. Decision making in vaccine hesitant parents and pregnant women - An integrative review. Int J Nurs Stud Adv. 2022;4:100062. doi: 10.1016/j.ijnsa.2022.100062 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Schue JL, Singh P, Fesshaye B, Miller ES, Quinn S, Karron RA, et al. Vaccine decision-making among pregnant women: a protocol for a cross-sectional mixed-method study in Brazil, Ghana, Kenya and Pakistan. Gates Open Res [Internet]. 2024 Aug 29 [cited 2024 Aug 30];8:94. Available from: https://gatesopenresearch.org/articles/8-94/v1 [DOI] [PMC free article] [PubMed]
  • 36.Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42(2):377–81. doi: 10.1016/j.jbi.2008.08.010 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Harris PA, Taylor R, Minor BL, Elliott V, Fernandez M, O’Neal L, et al. The REDCap consortium: Building an international community of software platform partners. J Biomed Inform. 2019;95:103208. doi: 10.1016/j.jbi.2019.103208 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Schue JL. Exploring Knowledge, Attitudes, and Practices Related to Vaccine Decision-Making among Pregnant People [Internet]. OSF; 2024 [cited 2024 Aug 19]. Available from: https://osf.io/g3yd2/
  • 39.Dempsey AF, Pyrzanowski J, Donnelly M, Brewer S, Barnard J, Beaty BL. Acceptability of a hypothetical group B strep vaccine among pregnant and recently delivered women. Vaccine. 2014;32(21). [DOI] [PubMed] [Google Scholar]
  • 40.Costa NS, Rio-Tinto A, Pinto IBF, dos Santos Silva Alvim DC, de Assis Rocha A, Oliveira LMA, et al. Changes in Group B Streptococcus Colonization among Pregnant Women before and after the Onset of the COVID-19 Pandemic in Brazil. Pathogens [Internet]. 2022 Sep 27 [cited 2025 Jul 23];11(10):1104. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609651/ [DOI] [PMC free article] [PubMed]
  • 41.Freitas FT de M, Romero GAS. Early-onset neonatal sepsis and the implementation of group B streptococcus prophylaxis in a Brazilian maternity hospital: a descriptive study. Braz J Infect Dis [Internet]. 2016 Nov 19 [cited 2025 Jul 23];21(1):92–7. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425498/ [DOI] [PMC free article] [PubMed]
  • 42.Carvalho AG, Rodrigues RS, Rodrigues MD, Oliveira LP de, Belém MGL, Ricarte MJVG, et al. Group B Streptococcus colonization prevalence and susceptibility profile in pregnant women in the Brazilian Amazon <span class=“so-article-trans-title” dir=”auto”> Translated title: Prevalência e perfil de suscetibilidade da colonização por Streptococcus do grupo B em gestantes da Amazônia Brasileira </span>. Revista Brasileira de Saúde Materno Infantil [Internet]. 2024 Jan 1 [cited 2025 Feb 24]; Available from: https://www.scienceopen.com/document?vid=f6d6205f-1fb0-4e63-91f7-a50e148e4bc5
  • 43.Silva LR da, Arruda LES de, Barreto I de JB, Aragão JVR de, Silva MLFI da, Lira G, et al. Geography and public health: analysis of the epidemiological dynamics of meningitis in Brazil, between 2010 and 2019. Rev Bras Epidemiol. 2024;27:e240031. doi: 10.1590/1980-549720240031 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Tsalta-Mladenov M, Dimitrova V, Georgieva D, Andonova S. Streptococcus agalactiae meningitis presenting with cerebral infarction in an adult patient: Clinical case and review. Neurology Asia [Internet]. 2022 Mar 31 [cited 2025 Feb 24];27(1):185–90. Available from: https://www.neurology-asia.org/system/index.php/neuro/article/view/705 [DOI] [PubMed]
  • 45.Kenchington AL, Lamont RF. Group B streptococcal immunisation of pregnant women for the prevention of early and late onset Group B streptococcal infection of the neonate as well as adult disease. Expert Rev Vaccines. 2017;16(1):15–25. doi: 10.1080/14760584.2016.1209113 [DOI] [PubMed] [Google Scholar]
  • 46.Romain A-S, Cohen R, Plainvert C, Joubrel C, Béchet S, Perret A, et al. Clinical and Laboratory Features of Group B Streptococcus Meningitis in Infants and Newborns: Study of 848 Cases in France, 2001-2014. Clin Infect Dis. 2018;66(6):857–64. doi: 10.1093/cid/cix896 [DOI] [PubMed] [Google Scholar]
  • 47.Vaciloto E, Richtmann R, Costa H de PF, Kusano EJU, Almeida MFB de, Amaro ER. A survey of the incidence of neonatal sepsis by group B Streptococcus during a decade in a Brazilian maternity hospital. Braz J Infect Dis [Internet]. 2002 Apr [cited 2025 Jul 23];6:55–62. Available from: https://www.scielo.br/j/bjid/a/jKhb7kghVHjcZv7vggynxZF/?lang=en [DOI] [PubMed]
  • 48.McClymont E, Wong JMH, Forward L, Blitz S, Barrett J, Bogler T, et al. Acceptance and preference between respiratory syncytial virus vaccination during pregnancy and infant monoclonal antibody among pregnant and postpartum persons in Canada. Vaccine [Internet]. 2025 Mar 19 [cited 2025 Feb 24];50:126818. Available from: https://www.sciencedirect.com/science/article/pii/S0264410X2500115X [DOI] [PubMed]
  • 49.Saper JK, Heffernan M, Simon N-JE, Davis MM, Macy ML. RSV Vaccination Intention Among People Who Are or Plan to Become Pregnant. Pediatrics. 2024;153(5):e2023065140. doi: 10.1542/peds.2023-065140 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Wang B, Lassi Z, Andraweera P, Chen G, Ong JJ, McMillian M. Pregnant women’s choices for preventing respiratory syncytial virus (RSV). Vaccine. 2025;48:126790. [DOI] [PubMed] [Google Scholar]
  • 51.Quincer EM, Gobezayehu AG, Belew ML, Endalamaw LA, Tesfaye YA, Shiferaw M. High intention to vaccinate against tuberculosis during pregnancy and lactation: understanding vaccine-specific maternal immunization acceptance in Amhara, Ethiopia. Pediatr Infect Dis J. 2025;44(2S):S135-40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Healy SA, Fried M, Richie T, Bok K, Little M, August A, et al. Malaria vaccine trials in pregnant women: An imperative without precedent. Vaccine [Internet]. 2019 Feb [cited 2025 Mar 17];37(6):763–70. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0264410X18316980 [DOI] [PMC free article] [PubMed]
  • 53.Gamain B, Chêne A, Viebig NK, Tuikue Ndam N, Nielsen MA. Progress and Insights Toward an Effective Placental Malaria Vaccine. Front Immunol [Internet]. 2021 Feb 25 [cited 2025 Mar 17];12:634508. Available from: https://www.frontiersin.org/articles/10.3389/fimmu.2021.634508/full [DOI] [PMC free article] [PubMed]
  • 54.Duffy PE, Gorres JP, Healy SA, Fried M. Malaria vaccines: a new era of prevention and control. Nat Rev Microbiol [Internet]. 2024 Dec [cited 2025 Mar 17];22(12):756–72. Available from: https://www.nature.com/articles/s41579-024-01065-7 [DOI] [PubMed]
  • 55.Battarbee AN, Stockwell MS, Varner M, Newes-Adeyi G, Daugherty M, Gyamfi-Bannerman C, et al. Attitudes Toward COVID-19 Illness and COVID-19 Vaccination among Pregnant Women: A Cross-Sectional Multicenter Study during August-December 2020. Am J Perinatol. 2022;39(1):75–83. doi: 10.1055/s-0041-1735878 [DOI] [PubMed] [Google Scholar]
  • 56.Karafillakis E, Paterson P, Larson HJ. My primary purpose is to protect the unborn child: understanding pregnant women’s perceptions of maternal vaccination and vaccine trials in Europe. Vaccine. 2021;39(39):5673–9. [DOI] [PubMed] [Google Scholar]
  • 57.Skjefte M, Ngirbabul M, Akeju O, Escudero D, Hernandez-Diaz S, Wyszynski DF, et al. COVID-19 vaccine acceptance among pregnant women and mothers of young children: results of a survey in 16 countries. Eur J Epidemiol. 2021;36(2):197–211. doi: 10.1007/s10654-021-00728-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Jaffe E, Lyerly AD, Goldfarb IT. Pregnant women’s perceptions of risks and benefits when considering participation in vaccine trials. Vaccine. 2020;38(44):6922–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Lyerly AD, Namey EE, Gray B, Swamy G, Faden RR. Women’s views about participating in research while pregnant. IRB. 2012;34(4):1–8. [PubMed] [Google Scholar]
  • 60.McQuaid F, Jones C, Stevens Z, Plumb J, Hughes R, Bedford H, et al. Factors influencing women’s attitudes towards antenatal vaccines, group B Streptococcus and clinical trial participation in pregnancy: an online survey. BMJ Open. 2016;6(4):e010790. doi: 10.1136/bmjopen-2015-010790 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Taylor MM, Kobeissi L, Kim C, Amin A, Thorson AE, Bellare NB, et al. Inclusion of pregnant women in COVID-19 treatment trials: a review and global call to action. The Lancet Global Health [Internet]. 2021 Mar [cited 2025 Mar 17];9(3):e366–71. Available from: https://linkinghub.elsevier.com/retrieve/pii/S2214109X20304848 [DOI] [PMC free article] [PubMed]
  • 62.Coleman MA, Dongarwar D, Ramirez J, Laracuente M-L, Livingston C, Ogu J, et al. Factors Impacting Vaccine Uptake during Pregnancy: A Retrospective Analysis. Int J MCH AIDS. 2022;11(2):e554. doi: 10.21106/ijma.554 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Krubiner CB, Faden RR, Karron RA, Little MO, Lyerly AD, Abramson JS, et al. Pregnant women & vaccines against emerging epidemic threats: Ethics guidance for preparedness, research, and response. Vaccine. 2021;39(1):85–120. doi: 10.1016/j.vaccine.2019.01.011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.World Health Organization. The Weekly Epidemiological Record (WER) [Internet]. 2022 [cited 2025 Feb 24]. Available from: https://www.who.int/publications/journals/weekly-epidemiological-record
  • 65.MacDonald NE, SAGE Working Group on Vaccine Hesitancy. Vaccine hesitancy: Definition, scope and determinants. Vaccine. 2015;33(34):4161–4. doi: 10.1016/j.vaccine.2015.04.036 [DOI] [PubMed] [Google Scholar]
PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004562.r001

Decision Letter 0

Giridhara Rathnaiah Babu

14 Jul 2025

PGPH-D-25-00806

Pregnant women’s attitudes and intentions toward tuberculosis, malaria, group B streptococcus, and respiratory syncytial virus vaccines in pregnant: Findings from pregnant women living in Brazil, Ghana, Kenya, and Pakistan

PLOS Global Public Health

Dear Dr. Limaye,

Thank you for submitting your manuscript to PLOS Global Public Health. After careful consideration, we feel that it has merit but does not fully meet PLOS Global Public Health’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

The reviewers raised concerns about methodological clarity, the rationale behind the survey, and the analysis. They requested clarification of the inclusion criteria (e.g., prior awareness of COVID-19 vaccines), justification for vaccine choices, and an explanation for dichotomizing Likert responses. Additionally, they questioned cross-country comparisons in a primarily attitude-descriptive survey. Ethical issues regarding participant expectations and the sharing of missing data information also need to be addressed.

Please submit your revised manuscript by Aug 28 2025 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at globalpubhealth@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pgph/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

We look forward to receiving your revised manuscript.

Kind regards,

Giridhara Rathnaiah Babu, MBBS, MPH, PhD

Academic Editor

PLOS Global Public Health

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Additional Editor Comments (if provided):

The reviewers raised concerns about methodological clarity, the rationale behind the survey, and the analysis. They requested clarification of the inclusion criteria (e.g., prior awareness of COVID-19 vaccines), justification for vaccine choices, and an explanation for dichotomizing Likert responses. Additionally, they questioned cross-country comparisons in a primarily attitude-descriptive survey. Ethical issues regarding participant expectations and the sharing of missing data information also need to be addressed.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Does this manuscript meet PLOS Global Public Health’s publication criteria?>

Reviewer #1: Partly

Reviewer #2: Yes

Reviewer #3: Yes

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2. Has the statistical analysis been performed appropriately and rigorously?-->?>

Reviewer #1: No

Reviewer #2: Yes

Reviewer #3: I don't know

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3. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)??>

The PLOS Data policy

Reviewer #1: No

Reviewer #2: Yes

Reviewer #3: Yes

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4. Is the manuscript presented in an intelligible fashion and written in standard English??>

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

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Reviewer #1: Thank you for asking me to review this paper which reports the findings of a cross-sectional survey, completed by pregnant women in four countries on their attitudes towards vaccinations. The paper reports an important area of study and I applaud the authors for their important message about the importance of inclusion of pregnant women in clinical trials. However, there are several issues I have identified in the paper, mostly around methods and expansion on why some of the questions have been asked, which would require revision prior to publication.

Title

• Title should include that this is a cross-sectional survey, i.e. “Findings from a cross-sectional survey of pregnant women…..”

Background

• Worth mentioning in the background that GBS can also result in death of the baby

• Background sets the scene nicely but would be helpful to expand a little on the final paragraph re women’s attitudes to vaccines – briefly mention any previous work and why this is an important question to answer, i.e. even if vaccines are made available in LMICs important to know whether they would be considered acceptable to those who they are intended for

• As this paper reports the results of a cross-sectional survey, as part of a wider programme of work, this should be specified at the end of the background section, rather than in the ‘participants, study setting and recruitment’ sub-section of Methods. It will make it clear that this study reports only the survey data, and that data collected from qualitative interviews is reported separately.

• The background section should include a clearly framed research question, with clearly specified objectives for the study.

Methods

• Please add a sentence that summarises the total number of sites/facilities that were involved

• Page 7, the sentence regarding sample size is unclear – ‘proportion of respondents with an attitude’. Surely everyone had an attitude, positive or negative, towards vaccines. Please be clearer here. What were the sample size assumptions based on?

• It’s unclear to me why formal statistical testing was undertaken and looking for a statistical difference between countries. For this kind of study, I would have expected to see descriptive statistics only reported.

• Data collection – were women provided with written participant information? Please make this clear

• Please explain the rationale for having “heard of Covid-19 vaccine” as an eligibility criteria for inclusion

• The countries who provided food box/transport renumeration – was this before or after completion of the survey?

• Future maternal vaccine intentions: Did you collect data on the reasons for the response choice for the question relating to their intentions? i.e. “I would not have no intentions of receiving the vaccine”…. Because……..

• Vaccine hesitancy – please explain the rationale for including a very specific question relating to the Covid-19 vaccination. I appreciate this is likely to set the scene since many women will have heard of this particular vaccine, but I think some context is required. Arguably, getting a vaccine for Covid-19 is quite different to GBS, for example.

• Priority maternal vaccine – please explain the rationale for inclusion of this question in the survey. Can the authors comment on the potential ethical implications of raising hope in women that (some of) these vaccines may become available in the future – how was this mitigated? In addition, did the authors collect any data on the past medical or family medical history? The answer to the question re priority maternal vaccine could be influenced by their own health or that of a family member – i.e. family member may have respiratory problems, so woman may be more likely to choose this vaccine if they thought it may prevent them developing respiratory issues

Results

• P values have been included to show differences between countries - but it's not clear why this is important. The p values don't add anything - it's clear there are differences by looking at the frequencies etc. Seeing whether there is a statistically significant difference between countries is of less importance. I would have expected to see the data in a survey such as this one being presented descriptively (e.g. means, medians etc.). The aims and objectives are not clearly specified - was it always the intention to look for between country differences?

• Table 2 is very unclear

• It would be helpful to add percentages to figure 1

• The quality of figure 3 makes it difficult to read – but I question what this figure adds. It looks like it reports the same data as in figure 2, in an alternative format

• The results present information that should be reported in the methods section. For example, line 381 on page 17. This is one example, but this happens throughout.

Discussion

• Given the apparent emphasis on comparison between countries, I would have expected to see discussion about what this could mean in practice in terms of distribution of vaccinations and the work needed with in-country policy-makers regarding procurement of vaccinations and implementation into the health systems

• Great to see the authors advocating for the inclusion of pregnant women in clinical trials

Other

• It is a journal requirement to make data publicly available – the manuscript does not include details of where the data is shared. In the submission information it states ‘data is available upon reasonable request’

Reviewer #2: Line 44 to 46: vaccine safety for baby has been repeated,

Line 157: you have mentioned COVID 19 vaccine decision making

Line 188: why having heard of the COVID-19 vaccine is an inclusion criteria? Isn't the study about TB, Malaria, GBS and RSV?

Line 259: same as above, the vaccine hesitancy section is all about COVID-19

Line 373: While the study provides useful insights into vaccine prioritization among pregnant women across countries, it remains unclear whether participants had adequate knowledge of the diseases or vaccine safety profiles. The absence of questions exploring their rationale limits the interpretability of these preferences. Most women have received high school education, when presented with a list of 4 vaccines , it is overwhelming and their choices reflect guesswork or based on whatever little they know or don't know about that disease. Without adequate knowledge about the disease, it's burden and consequences being informed, it is difficult to understand the rationale to understand vaccine acceptance study 4 different diseases.

Reviewer #3: In this study Rupali et al have explored the attitudes of pregnant women in 4 countries regarding the uptake of 4 plausible future vaccines. The topic is an important one and the study has been conducted well. Please find my comments and queries below.

Major comments

1. The study has been described as a mixed methods study. However, only quantitative surveys seem to have been conducted. Were there no interviews or focus group discussions done to understand the major emerging themes regarding the attitudes of the participants?

2. Why was knowledge on COVID-19 vaccine a requirement for inclusion in the study?

3. Of the many potential vaccine- preventable diseases, why these specific four vaccines were selected for the purpose of the study?

4. Why was the data collected using Likert scale dichotomized during analysis? This could have led to potential loss of information.

5. It is not clear from the methods section whether any information on the potential effects of these 4 diseases on pregnancy was imparted to the participants. The attitude of the study participants will definitely depend upon their perception of threat from each of these diseases for themselves as well as the baby. It is difficult to imagine that all the study participants had baseline knowledge about diseases caused by GBS or RSV. Even in the case of more well-known diseases like malaria or TB, their effect on pregnancy is not something which is widely known. Please explain.

6. In Discussion section (lines 404 to 408) the authors are attributing the favorable attitude of pregnant women for GBS vaccine to the high prevalence of this infection, antibiotic resistance and the disease related morbidity and mortality. Again, unless the information regarding these was provided to the participants, it is difficult to assume that these factors would have influenced their choices.

Minor comments

1. Please correct the repetition in the following statement found in abstract “Participants indicated that vaccine safety for the baby was the most important factor in their decision-making related to vaccine acceptance, followed by vaccine efficacy for the baby, and then vaccine safety for the baby.”

2. Please rephrase and correct the sentence “The sample size was determined with 80% power to find differences in proportions of respondents with an attitude between two groups with a 5% margin of error.” Proportion with an attitude??

3. Line number 200 is confusing. “members of the team from (blinded for review) through…”

4. “In Kenya, vaccine safety for the mother was chosen most frequently, and in Ghana, vaccine efficacy for the mother was chosen most frequently.” Use of the conjunction AND seems inappropriate here.

5. In lines 360 to 362 the use of terms like “least likely to definitely intend to receive” is very confusing to read.

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what does this mean? ). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy

Reviewer #1: No

Reviewer #2: Yes: Deepa R

Reviewer #3: Yes: Deepanjali S

**********

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Attachment

Submitted filename: Review.docx

pgph.0004562.s001.docx (15.8KB, docx)
PLOS Glob Public Health. doi: 10.1371/journal.pgph.0004562.r003

Decision Letter 1

Giridhara Rathnaiah Babu

6 Oct 2025

Pregnant women’s attitudes and intentions toward tuberculosis, malaria, group B streptococcus, and respiratory syncytial virus vaccines in pregnant: Findings from pregnant women living in Brazil, Ghana, Kenya, and Pakistan

PGPH-D-25-00806R1

Dear Dr. Limaye,

We are pleased to inform you that your manuscript 'Pregnant women’s attitudes and intentions toward tuberculosis, malaria, group B streptococcus, and respiratory syncytial virus vaccines in pregnant: Findings from pregnant women living in Brazil, Ghana, Kenya, and Pakistan' has been provisionally accepted for publication in PLOS Global Public Health.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they'll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact globalpubhealth@plos.org.

Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Global Public Health.

Best regards,

Giridhara Rathnaiah Babu, MBBS, MPH, PhD

Academic Editor

PLOS Global Public Health

***********************************************************

Reviewer Comments (if any, and for reference):

Reviewer's Responses to Questions

Comments to the Author

Reviewer #1: All comments have been addressed

Reviewer #3: All comments have been addressed

**********

publication criteria?>

Reviewer #1: Yes

Reviewer #3: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?-->?>

Reviewer #1: I don't know

Reviewer #3: I don't know

**********

4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)??>

The PLOS Data policy

Reviewer #1: No

Reviewer #3: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English??>

Reviewer #1: Yes

Reviewer #3: Yes

**********

Reviewer #1: Thank you for addressing feedback. I have no further comments.

Reviewer #3: The authors have addressed the issues raised

**********

what does this mean? ). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

For information about this choice, including consent withdrawal, please see our Privacy Policy

Reviewer #1: Yes: Eleanor Mitchell

Reviewer #3: Yes: Deepanjali S

**********

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    Attachment

    Submitted filename: Review.docx

    pgph.0004562.s001.docx (15.8KB, docx)
    Attachment

    Submitted filename: Response to Reviewers FVI.docx

    pgph.0004562.s003.docx (22.7KB, docx)

    Data Availability Statement

    There are ethical and legal restrictions which prevent the public sharing of minimal data for this study, because the data contain potentially identifiable participant information. Data for this study are available upon request via email from IRB contacts at the University of Campinas (cep@unicamp.br), Ghana Health Service (ethics.research@ghs.gov.gh), KEMRI (director@kemri.org), NBC Pakistan (nbcpakistan@nih.org.pk), and JHU IRB (BSPH.irboffice@jhu.edu) for researchers who meet the criteria for access to confidential data.


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