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Infectious Disease Reports logoLink to Infectious Disease Reports
. 2012 Feb 22;4(1):e17. doi: 10.4081/idr.2012.e17

Rubella antibody screening during pregnancy in an urban area of Northern Italy

Massimo De Paschale 1, Maria Teresa Manco 1, Alessia Paganini 1, Carlo Agrappi 1, Paola Mirri 1, Gabriella Cucchi 2, Barbara Saccani 2, Alberto Flores D'Arcais 2, Pierangelo Clerici 1
PMCID: PMC3892660  PMID: 24470924

Abstract

Various countries have implemented anti-rubella vaccination campaigns with the main aim of preventing congenital infection. In 2003, Italy joined the European WHO programme for the elimination of congenital rubella and issued a special healthcare plan, one of the objectives of which was to reduce the proportion of rubella-susceptible pregnant women to less than 5% by 2005. The aim of this study was to determine the percentage of seronegative pregnant women after the implementation of this plan. Anti-rubella IgG and IgM antibodies were sought in 2385 pregnant women who attended our hospital for serological screening between 1 July 2008 and 30 June 2010. They included 750 women of foreign origin (31.4%). Eight percent of the women were anti-rubella seronegative: 6.2% of the Italians and 11.7% of the non-Italians. Among the women of foreign origin, the percentage of seronegativity ranged from 5.6% of those coming from Eastern Europe to 17.7% of those coming from Latin America. The level of seropositivity among women of Italian origin is high, although the objective of ensuring less than 5% of susceptible pregnant women has not yet been quite reached in our area. However, particular attention needs to be given to women coming from geographical areas characterised by different epidemiologies and vaccination strategies because the percentage of seronegativity is in some cases double that of Italian women.

Key words: antibodies, pregnancy, screening, rubella, vaccination.

Introduction

Rubella infection generally leads to mild disease in children, but, if it occurs during early pregnancy, it can cause miscarriages or severe fetal malformations.1 The risk of foetal damage is greatest in the first trimester of pregnancy, but rapidly decreases after the twelfth week to only rare cases of deafness due to infections occurring during the 17th and 18th week.2

In order to prevent the onset of congenital rubella syndrome (CRS), various European countries have introduced vaccination campaigns based on two main strategies (or a combination of the two): the selective vaccination of adolescent girls and/or women of childbearing age, or the universal vaccination of boys and girls.3 In the first case, the selective vaccination of adolescent girls leaves susceptible males who may be responsible for continuing the circulation of the virus that can infect pregnant women who may not have been vaccinated. In the second case, inadequate vaccine coverage may allow the continuing circulation of the virus, prolong the time intervals between epidemics, lead to a higher incidence of the disease among older subjects, including women of childbearing age, and increase the risk of CRS.4,5 According to the WHO, at least 95% of children of both sexes need to be vaccinated before the transmission of rubella can be stopped.

The European WHO therefore issued a plan for eliminating congenital rubella6 with the aim of having less than one case of CRS per 100,000 live births by 2010. In order to reach this goal, it was planned to ensure at least 95% vaccine coverage among children aged 2 years, with at least one dose of vaccine in all administration units.7 Furthermore, additional vaccination strategies were foreseen for adolescents, women of childbearing age and immigrants, as well as recovery strategies for those children who were not vaccinated before.7

The vaccine was introduced into Italy at the beginning of the 1970s. Vaccination was initially recommended only for prepubescent girls (Ministerial Decree of 6 April 1976). The introduction of recombinant measles, mumps and rubella (MMR) vaccines in the 1990s led to the recommendation that all children of both sexes should be vaccinated before they are two years old (Ministerial Decree of 6 June 1995), and that their immunisation status should be assessed (and regularised if necessary) at the ages of 5–6 and 11–12 years, when they are administered other vaccines in accordance with the national vaccination schedule (Ministerial Decrees of 7 April 1999 and 13 July 1999).

Studies carried out in the 1990s estimated that about 56% of children were immunized with combined measles, mumps and rubella vaccine, depending on the region (vaccination coverage greater in Northern than in Southern Italy);811 this was reflected by the lower seronegative rates of women of childbearing age in Northern than in Southern Italy (6% vs 12%).12 By 2003, regional immunisation rates had increased to between 55% and 90%.9

In the same year, Italy joined the WHO European programme for the elimination of congenital rubella6 and issued a special healthcare plan (Agreement between the Central Government, Regions and autonomous Provinces of Trento and Bolzano regarding the National Measles and congenital Rubella Elimination Plan, 2003–2007. Unpublished data) . The aims of this plan were to ensure that an average of 95% of children aged less than two years had received a dose of MMR by 2006, and to reduce the proportion of rubella-susceptible pregnant women to less than 5% by 2005. It was also planned to vaccinate children aged more than two years and any adolescents who were still susceptible by undertaking an extraordinary recovery programme and introducing a second dose of MMR vaccine. The strategies aimed at women of childbearing age were to vaccinate susceptible women before they became pregnant; to screen pregnant women for anti-rubella antibodies as early as possible and, if they were seronegative, to repeat the screening every 4-6 weeks at least until the fifth month; and to vaccinate susceptible women during the postpartum period. Particular attention was also given to protecting recent immigrants who have reduced access to healthcare services.

The aim of this study was to determine the percentage of susceptible pregnant women in the period 2008–2010 in order to verify whether this objective of the plan had been reached in our area located in Lombardy, a region of Northern Italy.

Materials and Methods

Between 1 July 2008 and 30 June 2010, 2385 pregnant women underwent a first serological screening for anti-rubella IgG and IgM antibodies: 2255 (94.5%) were in the first trimester of pregnancy, 69 (2.9%) in the second and 61 (2.6%) in the third. Seven hundred and fifty

(31.4%) were non-Italians: 251 came from Eastern Europe, 171 from the Middle East and the Maghreb, 130 from Latin America, 66 from the Indian sub-continent, 58 from China and the Far East, 55 from South-Equatorial Africa, and 19 from Western Europe.

Anti-rubella IgG and IgM antibodies were detected by means of enzyme linked immunoassays (ETI-RUBEK-G PLUS and ETI-RUBEK-M reverse plus, DiaSorin, Saluggia, Italy). Cut-off value used for the determination of IgG levels was 10 IU/mL. IgM positivity was confirmed by means of an ezyme-linked fluorescent assay (ELFA; VIDAS RUB IgM, BioMérieux, Marcy l'Etoile, France); in addition, IgG avidity was determined by modifying the IgG detection test (VIDAS, RUB IgG II, BioMérieux, Marcy l'Etoile, France) as suggested by Eggers.13 In the case of IgM positivity, the woman's general practitioner was contacted and advised to evaluate the case and refer the patient to a Reference Centre.

The data were statistically analysed using the χ2 test, Fisher's exact test, and Student's t test.

Results

Two thousand, one hundred and ninety-five women (92.0%) were IgG positive and 10 (0.4%) IgM positive (all in the first trimester of pregnancy); ELFA confirmed eight of the IgM-positive cases. All of these women had high levels of IgG avidity. Their general practitioners were contacted and the women were referred to a Reference Centre. We had information on only 4 of 8 women, all excluding an infection during pregnancy. The 4 women had their delivery in our hospital and the children are currently healthy.

Table 1 shows that the differences in the seroprevalence data between the Italian and non-Italian women were statistically significant in the case of IgG (P<0.01), but not in the case of IgM.

Table 1. Seropositivity for anti-rubella IgG in pregnant women of Italian and foreign origin (2008-2010).

Origin No. Anti-rubella antibodies
IgG positive % 95% CI Confirmed IgM positive % 95% CI
Italian 1635 1533 93.8 92.63-94.97 7 0.4 0.09-0.71
Foreign 750 662 82.3 79.57-85.03 1 0.1 0.00-0.33
P <0.01 NS
Total 2385 2195 92.0 90.91-93.09 8 0.3 0.08-0.52

NS, not significant

Table 2 shows the geometric mean IgG values of the IgG-positive women (≥10 IU/mL); the difference between the women of Italian and foreign origin is statistically significant (P<0.01).

Table 2. Geometric mean IgG values in pregnant women of Italian and foreign origin who were positive for anti-rubella IgG (≥10 IU/mL).

Origin No. Anti-rubella antibodies (IU/mL)
Geometric mean 95% CI
Italian 1533 58.5 56.7-60.4
Foreign 662 51.7 49.2-54.4
P <0.01
Total 2195 56.4 54.9-57.9

A total of 8% (95% CI: 6.91-9.09) of the women were negative for anti-rubella antibodies: 6.2% of the Italians (95% CI: 5.03-7.37), and 11.7% of the non-Italians (95% CI: 9.40-14.00). In terms of the country of origin, seronegativity ranged from 5.6% among the women from Eastern Europe to 17.7% among those from Latin America (Table 3). All of the differences from the 6.2% of Italian women are statistically significant except in the case of the women coming from the Indian sub-continent and rest of Europe.

Table 3. Seronegativity for anti-rubella IgG in pregnant women by geographical origin (2008-2010).

Origin No. Anti-rubella antibodies P*
Negative % 95% CI
Africa 55 8 14.5 5.19-23.81 <0.05
China and the Far East 58 10 17.2 7.49-26.91 <0.01
Eastern Europe 251 14 5.6 2.76-8.44 NS
Western Europe 19 3 15.8 0.00-32.20 NS
Indian sub-continent 66 5 7.6 1.21-13.99 NS
Middle East and the Maghreb 171 25 14.6 9.31-19.89 <0.01
Latin America 130 23 17.7 11.14-24.26 <0.01
Italy 1635 102 6.2 5.03-7.37
*

vs Italian women; NS, not significant

In relation to age, the differences between the Italian and non-Italian women are statistically significant only in the age group 21–30 years (Table 4). Within the two groups of Italian and non-Italian women, the differences between the various age groups are not statistically significant.

Table 4. Seronegativity for anti-rubella IgG in pregnant women of Italian and foreign origin by age (2008-2010).

Age (years) Origin
Italian Foreign P Total
No. % (95% CI) No. %(95% CI) No. % (95% CI)
8.0 11.4 10.0
≤20 2/25 (0.00-18.63) 4/35 (0.87-21.93) NS 6/60 (2.41-17.59)
6.1 13.5 9.5
21-30 30/490 (3.98-8.22) 56/415 (10.21-16.79) <0.01 86/905 (7.59-11.41)
6.0 9.2 6.7
31-40 63/1050 (4.56-7.44) 26/282 (5.83-12.57) NS 89/1332 (5.36-8.04)
10.0 11.1 10.2
>40 7/70 (2.97-17.03) 2/18 (0.00-25.61) NS 9/88 (3.88-16.52)
6.2 11.7 8.0
Total 102/1635 (5.03-7.37) 88/750 (9.40-14.00) <0.01 190/2385 (6.91-9.09)

NS, not significant

Discussion

In 2003, Italy joined the European WHO programme aimed at eliminating congenital rubella by 20106 and issued a special healthcare plan. Among other things, this plan had the objectives of ensuring that there would be at least 95% vaccination coverage by the end of the second year of life and that fewer than 5% of pregnant women would be susceptible to the disease. As far as the first objective is concerned, partial data of the Ministry of Health for 2009 indicate a general coverage of 89.9%, with regional variations of between 70.8% and 95.5% (94.8% in Lombardy, www.salute.gov.it). Before the implementation of the plan, sero-prevalence among women of childbearing age and pregnant women in Italy was about 90%, with higher values in Northern than in Southern Italy.10,11,14,15 These data were in line with European data indicating higher sero-prevalence levels in Northern than in Southern Europe.12,1618

Since the implementation of the healthcare plan in our area, the seroprevalence level among pregnant women has been high (92%) without any differences between age groups, but has not substantially changed from before its implementation.12 The objective of ensuring that fewer than 5% of pregnant women are susceptible to the disease has therefore not yet been reached although it is near (about 6%). It is necessary to bear in mind that only one dose was administered in Italy in the past and, although the difference is slight, one dose is less efficacious than two.19 Furthermore, as what is observed today is the result of vaccinations given some time ago, the antibodies may have been lost. It is known that antibody levels decline over time after vaccination and after natural infection; minimal annual antibody decay rates of −2.9% was reported in the literature20 although, 15–20 years after vaccination, rubella seropositivity still ranges from 92% to 97%.2123

However, when comparing published data, it is important to consider the antibody titre used as an index of positivity. For example, in one study conducted 20 years after vaccination (with two doses), all of the subjects were considered positive with levels of more than 4 IU/mL; however, 17% had levels of less than 10 IU/mL and 36% had levels of less than 15 IU/mL.24 As it has been suggested that protection is provided by levels of 10-15 IU/mL25,26 because women with lower antibody values can still be considered at risk of developing CRS, we defined positivity as levels of ≥10 IU/mL. Consequently, the fact that 6% of our Italian women were seronegative may have been due to their missing the vaccination programme, an incomplete antibody response, or a decline in antibodies over time. Further-more, this value is in line with the WHO directives indicating the need to ensure >90% vaccination coverage in women of childbearing age.27

Things are different in the case of non-Italian women coming from countries with different epidemiologies and vaccination strategies. Increasing immigration involves the arrival of women coming from areas where the level of vaccination may be lower, which increases the pool of seronegative women. We found that percentage seronegativity among the women of foreign origin in our study was in some cases more than double that among Italian women. This a well-known problem in Europe:18,28 the European WHO has made it the subject of specific indications,7 and it was emphasised in the healthcare plan of the Italian Ministry of Health. Our own findings underline its importance because almost one-third of the pregnant women were born abroad, which is in line with official Italian data showing that, over the last few years, there has been an increase in immigration above all from non-EU countries.29 It is therefore necessary to make further efforts in this direction as the antibody screening and the vaccination of all women of childbearing age, new mothers and women who make a termination of pregnancy who have no serologic evidence of immunity or a documented vaccination.

In relation to acute infection, we found that 0.3% of our pregnant women were IgM positive, with no significant difference between the Italian and non-Italian group. However, as it has been reported that the IgM test can lead to false-positive results in patients with other ongoing infections (parvovirus or mononucleosis) or rheumatoid factor,30 and that IgM antibodies may remain for as long as one year or more after a first natural infection, asymptomatic re-infection or vaccination,31,32 we determined IgG avidity.3334 All of our IgM-positive women showed a high level of IgG avidity which, given the test used and the time of sampling, suggested an infection occurring before conception. However, given the variability of IgG maturation (which may be brief in some cases),3335 we referred the patients to Reference Centres for further investigation. Unfortunately, we had information about only half of these cases which, nevertheless, excluded an infection during pregnancy and this was supported by the birth in our hospital of currently healthy children.

In conclusion, our data show high levels of anti-rubella antibodies among Italian pregnant women in our area. However, particular attention should be paid in the case of women coming from geographical areas with different epidemiologies and vaccination strategies, whose access to healthcare services may be reduced for various reasons, such as language, culture, bureaucracy, etc. In these cases, special efforts need to be made to overcome these gaps and facilitate the antibody screening and vaccination.

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