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. 2019 Nov 15;98(46):e17969. doi: 10.1097/MD.0000000000017969

Abnormal IL-10 levels were related to alanine aminotransferase abnormalities during postpartum in HBeAg positive women with chronic hepatitis B

Ming Wang a,b, Ying Hou a, Shi-Hui Meng c, Bo Yang a, Ping Yang a, Hua Zhang a, Yunxia Zhu a,∗
Editor: Sherief Abd-Elsalam
PMCID: PMC6867749  PMID: 31725660

Supplemental Digital Content is available in the text

Keywords: alanine aminotransferase, hepatitis B e-Antigen, interleukin-10, postpartum

Abstract

Alanine transaminase (ALT) abnormalities are common in chronic hepatitis B (CHB) carriers during postpartum period. Disturbances in cytokines are considered to be associated with hepatitis Flares. There are limited data on cytokines changes in HBeAg positive patients with ALT abnormalities.

This is an observational study. Pregnant patients with hepatitis B e-antigen (HBeAg) positive were enrolled from January 2014 to September 2018. Patients were assigned into three groups based on ALT levels in postpartum 6 to 8 weeks: ALT in normal range, ALT in 1 to 2-fold upper limits of normal (ULN) and ALT >2-fold ULN. Serum cytokines, ratios of regulatory T cells, and the concentration of cortisol were collected and compared among the three groups.

Of the 135 mothers enrolled, 80.7% (109/135) completed the postpartum 6-week study. 13.8% (15/109) patients had postpartum ALT higher than 2∗ULN, 27.5% (30/109) patients had ALT in 1 to 2∗ULN and 58.7% (64/109) patients had ALT in normal range. Compared to control group, patients with ALT >2∗ULN had a higher IL-10 level (P < .05). No differences of IL-10 levels were found in the comparison of other inter comparison among three groups. No differences were found in the levels of other collected serum cytokines, cortisol, and regulatory T cells among three groups. On multivariate analysis, abnormal IL-10 level was independent risk factor for postpartum ALT elevating >2∗ULN. At the same time, the incidence of postpartum ALT elevated >2∗ULN were higher in patients with abnormal elevation IL-10 level than in patients with normal IL-10 level (14/68 vs 1/41, P = .008).

CHB patients with postpartum ALT abnormalities show higher IL-10 level and postpartum ALT abnormalities were mainly occurred in patients with abnormal IL-10 level. IL-10 may be an underlying predictor and treatment target of hepatitis B, and further studies are needed.

1. Introduction

Chronic hepatitis B virus (HBV) infection is an epidemic that is associated with cirrhosis and liver cancer.[1] Without intervention, 80% to 90% of infants born of hepatitis B e-antigen (HBeAg) positive mothers may be infected with HBV.[2] After the widespread use of the HBV vaccine combined with hepatitis B immunoglobulin G. The mother to child transmission rate (MTCT) has been reduced from 90% to ∼ 5% to 10%.[3,4] Previous studies indicated that inhibiting HBV replication with lamivudine (LAM), telbivudine (LdT) or tenofovir disproxil fumarate (TDF) during late pregnancy in HBeAg positive mothers with high viremia could further reduce the risk of MTCT.[5–7] However, postpartum ALT level elevation is common in CHB patients, which ranged from 10% to 57%.[8,9] In a study, 45 women with postpartum ALT level exceeding two times the upper limit of normal and HBV DNA level that had decreased more than 3∗lgIU/mL or HBeAg titer that had decreased more than 50% were switched to peg-IFNα and adefovir (CPIA) for 96 weeks. 91.1% (41/45) of them achieved a virological response, 55.6% (25/45) achieved HBeAg clearance or seroconversion, and 26.7% (12/45) achieved hepatitis B surface antigen (HBsAg) clearance or seroconversion. There were no cases of significant deterioration of liver function.[10] Although mild-to-moderate elevations of ALT levels during pregnancy have not been linked to pregnancy complications in mothers with CHB,[11] a recent study reported that severe ALT flares can cause maternal death.[12] Then, the postpartum ALT flares may mean a chance of better treatment or risk of liver deterioration.

The mechanism of ALT flares in these patients has not been fully understood. ALT flares or exacerbations are mainly observed in mothers with elevated ALT or HBV DNA levels ≥5 log10 IU/mL at delivery.[12] In pregnancy, immune alterations such as regulatory T (Treg) cells expansion and distinct regulation of Th1, Th2, and Th17 cytokines occur to prevent fetus rejection.[13,14] Maternal immune responses and CHB may alter the Th1/Th2 cytokine ratio during pregnancy. Cytokines are mediators of inflammation, indicate immune activation, and play a role in viral clearance.[15] Previous reports suggested that immunological changes during pregnancy may stimulate HBV clearance in highly viremic mothers.[8] It is hypothesized that postpartum hepatic flares in HBV or autoimmune hepatitis are due to immune system reactivation after parturition.[16,17] We selected patients who received antiviral treatment during pregnancy and compared their cytokines in different postpartum ALT groups. We aimed to study the relationship between postpartum ALT abnormalities and cytokines during postpartum non-treatment patients with high viremia.

2. Study methods

2.1. Design and patient selection

This is an observational case–control study in which patients were recruited from a tertiary care hospital, Beijing Youan Hospital in China between January 2014 and September 2018. The trial was approved by the institutional ethics review committee (approval number: Jing-you-ke-lun-zi [2016]15) and has been registered on the Chinese Clinical Trial Registration (no. ChiCTR-OIC-17010869). Pregnant women fulfilling the inclusion and exclusion criteria were offered participation in the study. All CHB pregnant carriers were assessed in the second trimester and followed until 6 to 8 weeks postpartum. Patients were assigned into three groups based on the ALT in postpartum 6 to 8 weeks: control (normal postpartum ALT levels), 1 to 2 ULN postpartum ALT levels and >2 fold ULN postpartum ALT levels. Serum quantitative hepatitis B virus (HBV) markers, HBV-DNA, ALT, cytokines, ratios of regulatory T cells and the concentration of cortisol were collected and compared among the three groups.

Beijing Youan Hospital is the appointed hospital by the department of health in Beijing to evaluate mothers with hepatitis B. Pregnant mothers were screened for the following criteria of eligibility: age between 20 and 45 years, HBsAg and HBeAg positivity, and HBV DNA levels above 5 log10 IU/mL, gestational age 24 to 28 weeks, Key exclusion criteria included ALT ≥80 U/mL (ULN = 40 U/mL); co-infection with hepatitis C, D, E, or HIV; evidence of hepatocellular carcinoma or cirrhosis; concurrent treatment with immune modulators, cytotoxic drugs, or steroids; evidence of fetal deformity by ultrasound examination.

2.2. Study procedures and data collections

Chronic Hepatitis B (CHB) was diagnosed according to the provincial prenatal screening program by the presence of HBsAg in serum, as described. The study consents were obtained before enrolment. The study was conducted according to International Conference Harmonization Good Clinical Practice guidelines and the Declaration of Helsinki. All mothers who agreed to participate in the study received antiviral therapy (LDT 600 mg/d or TDF 300 mg/d) from 24 to 28 weeks as recommended by the national guidelines in China for the timing of initiating on preventing mother to child transmission (MTCT). Patients were followed at 4-week intervals before the due date and the 6 to 8 weeks after delivery.

Clinical data recorded included age, ALT, HBV-DNA, HBV-markers, cortisol, ratio of regulatory T cells, and cytokines. A significant ALT flare was defined as >2-fold upper limits normal. The cytokines were detected with Bio Plex cytokine assay. According to the assay manufacturers, the sensitivity (expressed as the minimum detectable dose) and the upper limit of detection, respectively, for the various assays are: regulator T cells (5–10%), IL-2 (0 pg/mL, 99.44 pg/mL), IL-4 (0 pg/mL, 3.25 pg/mL), IL-6 (0 pg/mL, 8.53 pg/mL), IL-8 (0 pg/mL, 116.07 pg/mL), IL-10 (0 pg/mL, 1.53 pg/mL), INF-γ (0 pg/mL, 124.08 pg/mL), TNF-α (0 pg/mL, 60 pg/mL), and GM-CSF (0 pg/mL, 122.19 pg/mL).

2.3. Outcome measurements and endpoints

This study aimed to compare the concentrations of various cytokines, the ratio of regulator T cell, and cortisol in plasma samples in different postpartum ALT levels in patients with high viremic on-treatment.

2.4. Statistical analysis

In our trial, the mean value of IL-10 was 11.5±4.8 pg/ml in CHB patients and 4.8 ± 0.4 pg/mL in immune tolerant patients. Based on the data, 15 patients with ALT abnormal and 64 patients in immune tolerant phase could achieve more than 90% power to a significance level of 0.05 both one-tailed and two-tailed. Considering the incidence of Alanine aminotransferase flares was observed 17.1% to 45% in LdT or TDF treated mothers[6] and 20% drop-out rates, 126 cases were a reasonable least sample size.

Baseline characteristics and laboratory results were summarized for the three groups utilizing descriptive statistics, including percentage, means ± standard deviation (SD). Statistical analysis was performed using analyzed by SPSS 23.0 (SPSS, Inc., NYC, IBM) and GraphPad Prism Version 7.0 (GraphPad, La Jolla, CA). For the quantitative variable, the one-way ANOVA was used to compare three group differences. For categorical variables, the Kruskal–Wallis rank sum test was used for three group comparisons. Student's t test was used to assess continuous variables of two groups. Multivariate classification logistic regression was used to adjust IL-10 on predicting ALT elevation. Abnormal cytokine values were replaced with 1 and normal cytokine values were replaced with 0 during regression. The significance level was set at P < .05.

3. Results

3.1. Study population

Our study screened 159 CHB patients with HBeAg positive during the second trimester, 6 patients had ALT higher than 2∗ULN at baseline and 153 patients were in the immune tolerant phase (ALT < 2∗ULN). Of the 153 patients in immune tolerant phase, 135 patients started antiviral treatment after baseline research blood sample collection and 18 patients were not administered antiviral drugs. 109 of 135 patients completed the study (Fig. 1). At the time of postpartum follow-up, the ALT of 15 patients were increased more than 2∗ULN (177.81 ± 166.53 IU/L), 30 patients from I ULN to 2 ULN (55.82 ± 10.92 IU/L), and 64 patients in the normal range (26.27 ± 7.04 IU/L). Patients disposition is shown in Figure 1. The mean (SD) gestational weeks of delivery were 38.47 ± 1.41, 39.16 ± 1.05, 39.45 ± 1.33 weeks (P = .036) in three groups respectively, and the time of postpartum follow-up were 6.33 ± 1.23, 6.74 ± 1.15, 6.95 ± 2.32 weeks (P = .524) after delivery. Patients with postpartum ALT elevation had a higher HBV level in the baseline and lower HBV level in the postpartum, indicating more patients stepped into immune clearance phase (Table 1).There were no differences in the levels of HBsAg, HBeAg, and ALT, except the higher HBV-DNA in the patients with postpartum ALT elevated more than 2∗ULN.

Figure 1.

Figure 1

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Flowchart exhibiting the selection of the study population (n = 135) after excluding the patients who had ALT elevated ≥ 2ULN at baseline and not received antiviral patients. ULN = upper limits normal.

Table 1.

Comparison of pregnant and postpartum clinical information in patients with different postpartum ALT levels (n = 109).

3.1.

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3.2. Serum IL-10 flares are frequent in CHB carriers with postpartum ALT flares

We tested Th1 (IL-2, IFN-γ, TNF-α), Th2 (IL-4, IL-6, IL-10), Treg (IL-10) and mononuclear macrophage-related (IL-8, GM-CSF) serum cytokines previously reported to be associated with CHB flares. There was no significant difference in the levels of IL-2, IL-4, IL-8, IL-10, IFN-γ, TNF-α, GM-CSF, Treg, and cortisol (P > .05). However, IL-10 level was higher in patients with ALT elevating than in patients with normal ALT (P < .05) (Fig. 2A). To better understand whether IL-10 values can predict postpartum ALT elevation, we performed multivariate classification logistic regression analysis to compare the cytokine values of mothers with postpartum ALT higher than 80 IU/L to those of mothers who were in tolerant phase. After adjusting for the other cytokine variables listed in Supplementary Table S2, abnormal IL-10 was an independent predictor for postpartum ALT elevation (Wald = 3.995, Exp [B] = 11.887, 95% CI:[1.049, 134.653], P = .034) (see Table. Supplemental Table S1. Supplemental Table S1. Multiple variable logistic analysis on the postpartum abnormal ALT (>2ULN) with postpartum cytokines). After adjusting for the age, genotype, postpartum HBsAg, postpartum HBeAg, and postpartum HBV DNA levels, abnormal IL-10 was still the independent predictors for postpartum ALT elevation (Wald = 4.450, Exp [B] = 10.894, 95%CI:[1.184, 100.209], P = .035) (see Table. Supplemental Table S2. Multiple variable logistic analysis on the postpartum abnormal ALT (>2ULN) with postpartum IL-10).

Figure 2.

Figure 2

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The relationship of abnormal postpartum IL-10 levels with abnormal ALT. (A) Patients with postpartum ALT abnormalities (15 patients with ALT > 2∗ULN and 30 patients with ALT elevated in 1–2∗ULN) show higher IL-10 levels than control (64 patients with ALT in normal range); (B) patients with IL-10 abnormalities (n = 68) had a higher postpartum ALT levels than patients with IL-10 in normal range (n = 41). ALT = alanine aminotransferase, G-CSF = granulocyte colony stimulating factor, IL = Interleukin, INF-γ = Interferon-γ, TNF-α = Tumor necrosis factor-α, ULN = upper limits normal.

3.3. More ALT abnormalities in patients with Serum IL-10 abnormalities

To further explore the relationship of postpartum IL-10 with postpartum ALT flare, we compared the ratio of postpartum ALT flares between patients with IL-10 in the normal range and patients with IL-10 elevating higher than the normal range. In patients with normal IL-10 level, ALT in 1 patient was ALT flares (>80 U/L), 11 were mildly to moderately elevated (40–80 U/L), 29 were within the normal range (≤40 U/mL). In patients with elevated IL-10 level, ALT in 14 patients were ALT flares (>80 U/L), 20 were mildly to moderately elevated (40–80 U/L), 35 were within the normal range (≤40 U/mL). Statistically significant differences were seen in elevated postpartum IL-10 patients compared to normal postpartum IL-10 patients (P < .05) (Fig. 2B; Table 2). To further validate the relationship of IL-10 and ALT flare, we compared the ratio of ALT flares before delivery between patients with IL-10 in the normal range and patients with abnormal IL-10 elevation. Compared to patients with normal IL-10, more patients had abnormal ALT in abnormal IL-10 group. No difference of HBV-DNA levels between two groups of different IL-10 levels (see table. Supplemental Table S3. Frequency of ALT abnormalities in pregnant patients with abnormal IL-10 levels before delivery (n = 109)). In patients with IL-10 elevation before delivery, 2 of 66 patients had ALT elevating more than 2∗ULN, 5 of 66 patients had ALT elevating to 1–2ULN, 59 of 66 patients had ALT in normal range. However, in 43 patients with in normal IL-10 before delivery, only 1 patient had ALT elevating to 40.7 IU/L and the remaining 42 patients had ALT in normal range.

Table 2.

Frequency of ALT abnormalities in patients with abnormal postpartum IL-10 levels (n = 109).

3.3.

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4. Discussion

In previously published studies, 10% to 57% treated mothers experienced ALT flares[7,8] and 28.27% untreated CHB mothers were observed with abnormal ALT levels[12] after delivery. However, factors that can predict ALT flares during the postpartum period were still unknown. Cytokines are a complex and pleiotropic group of cell-signaling proteins that involve proliferation, maturation, migration, differentiation, activation, chemotaxis of immune cells, and predominantly responses to viral infections.[18] The production of pro-inflammatory cytokines (e.g., IL-2, IFN-c, TNF-a) are associated with Th1 cells and responsible for cell-mediated immunity, such as cytotoxic damage. By contrary, anti-inflammatory cytokines (e.g., IL-4, IL-5, IL-6, IL-9, IL-10) are usually produced by Th2 cells and promote humoral immunity.[19] No studies have reported on the relationships of postpartum ALT elevation and cytokine abnormalities in off-treatment postpartum populations.[20,21] Our research showed the serum levels of IL-10 were higher in postpartum patients with ALT abnormalities.

In the immune tolerance phase, some HBV infected patients remain HBeAg positive with high levels of serum HBV DNA but with few or no symptoms, normal ALT levels, and minimal histological activity in the liver.[22] When the tolerogenic effect is lost during the immune tolerance phase, immune mediated lysis of infected hepatocytes occurs, along with elevations in ALT levels. However, recent immunological studies challenge the concept of both immune tolerance and lack of disease activity based on clinical markers.[23,24] It has been suggested that rapid changes in the levels of maternal corticosteroids during postpartum period lead to active immunological responses to HBV.[13] But no differences were found in the levels of cortisol among three groups in our study. We found IL-10 levels were higher in patients with ALT elevation than in patients with normal ALT (P < .05). Within the liver, IL-10 comes from many cells, such as Toll-like receptor activated Kuppfer cells, LSEC primed CD4 +T cells, CD4+CD25+Foxp3+ and antigen-induced CD8 +T cells.[25,26] Increasing evidence has demonstrated that virus-specific T cells (i.e., CD8+CTL and CD4+Th cells) play a central role in the clearance of HBV.[27–29] After adjusting for the other cytokine variables, abnormal IL-10 was an independent predictor for postpartum ALT elevation. A previous study[30] showed that IL-10 levels were significantly positively correlated to HBV DNA load and ALT levels in the HBeAg-negative patients. After adjusting for the age, genotype of HBV, postpartum HBsAg, postpartum HBeAg, and postpartum HBV DNA levels, abnormal IL-10 was still the independent predictors for postpartum ALT elevation.

A successful pregnancy needs maternal immune suppression and fetal tolerance resulted from a shift from Th1-mediated cytotoxic attacks to Th2-mediated anti-inflammatory responses to foreign fetal cells.[31] IL-10 is a negative regulator of inflammation which tends to be raised in normal pregnancies[32] and reduced in preterm delivery pregnancies. Serum cytokine levels are dynamic and involve continuous modulation of cytokine balance by both exogenous (e.g., pregnancy-induced hypertension or gestational diabetes) and endogenous (e.g., progesterone) factors. The Th2-biased response resolves to pre-pregnant ratios by 4 weeks postpartum.[33] Besides, increased IL-10 seems to offer some degree of protection in normal pregnancy. The reduced IL-10 levels seen in preterm delivery and high-risk patients could be permissive of an excessively inflammatory, destructive local Environment.[34] Compared to placebo in the third trimester, IL-10 levels were increased in women who received progesterone.[35] The time of postpartum follow-up was 6.33 ± 1.23, 6.74 ± 1.15, 6.95 ± 2.32 weeks after delivery in our study when the influence of progesterone on cytokine attenuated. However, similar outcomes of more ALT abnormalities occurred in patients with elevated IL-10 than patients with IL-10 in normal ranges before delivery in our study.

However, mechanisms underlying the association of IL-10 and the cytoxic effects on liver cells are not fully understood. Th2 cytokines (IL-4, IL-6, and IL-10) can attenuate inflammatory responses which include the suppression of other cytokine production, the alteration of professional antigen presenting cells’ function and proliferation of CD4 and CD8 T cells.[36] Abnormal ALT is preceded by the change of immunological status suitable for active viral replication. In previous study, the parallel increase of serum IL-10 and HBV DNA levels suggested that IL-10 may trigger the surge of viral load by both suppressing antiviral inflammatory activity and enhancing viral replication. Elevated IL-10 has been repeatedly reported in patients with CHB and has been correlated with increased disease severity and viral load.[37] However, both higher IL-10 levels and lower HBV-DNA levels were found in our patients with ALT >2ULN than in immune tolerant patients. More patients had abnormal ALT in patients with abnormal IL-10 than in patients with normal IL-10 levels. Previous studies showed that increased expression of IL-10 is the primary factor that causes chronic HBV infection[30] and blockage of the IL-10 receptors could recover HBV specific CD8+ T cell response, accelerate virus elimination, and suppress the chronicity of viral infection.[37,38] IL-10 can induce the activation and proliferation of B cells and NK cells and enhance the cytotoxicity of CD8+ T cells, while inhibiting the production of IFN-γ selectively without changing the cytotoxicity of NK cells. In other studies, elevated serum IL-10 (Th2 cytokine) was correlated with early spontaneous seroconversion and degree of liver inflammation.[39] The expression of IL-10 is affected by the polymorphisms in the regulatory regions.[40] Haplotype carrying the homozygous ATA had low level of IL-10 while haplotype carrying the homozygous GCC had high level of IL-10. Meanwhile, the ACC (−1082, −819, and −592) haplotype could improve individuals’ anti-hepatitis B surface antigen (anti-HBs) antibody production to almost twice of individuals without this haplotype.[41] The mutation from −592G into −592A could enhance HBV susceptibility, while mutation from −1082A into −1082G could reduce HBV susceptibility. Mutation into −1082G allele was the protective factor against HBV infection, and the SNPs of IL-10 at −592 and −1082 sites were associated with HBV infection.[42,43] Wu et al[44] found that the polymorphisms of IL-10–1082 G/G genotype have correlation with lower HBV viral load and earlier HBeAg seroconversion. Different polymorphisms might explain the conflicting results between different results. In patients with abnormal IL-10 level, it is unclear whether the IL-10 elevation was the reflection of T-cell responses or IL-10 elevation lead to inflammatory activity and ALT elevation. This finding favors the close relationship between IL-10 levels and T cell cytotoxicity on HBV-infected liver. IL-10 could be a likely predictive marker for postpartum ALT elevation in patients with CHB virus. Besides, IL-10 may also be an underlying target for the control of HBV infection.

There are several limitations in our study. First, the sample size of this study was relatively small. Based on the data of our trial, 15 patients with ALT abnormal and 64 patients in immune tolerant could achieve 90% power at the significance of .05 both one-tailed and two-tailed. However, n the previous study,[45] mean value of IL-10 was 7.48 [3.10, 18.00] pg/mL) in CHB patients and 5.02 [2.98, 10.11] pg/mL in immune tolerant patients, the least patients were 17 patients in CHB group and 68 patients in tolerant phase at a significance level of .05 (one-tailed) and 80% power. The patients in previous study had a higher standard deviations than in our patients, which may relate to different methods of detection, higher ALT levels in previous study and individual difference. Second, we did not detect the polymorphisms of different patients in our study. Third, the immune status of patients with 1–2ULN is unclear since penetration biopsy of the liver is contraindicated in pregnant or postpartum women. There was no significant difference in the ratios of levels of postpartum IL-10 between patients with ALT higher than 2∗ULN and patients with ALT within the range of 1–2∗ULN. Some patients with ALT elevating in 1–2ULN might had undergone the peak ALT value higher than 2∗ULN Also some patients with ALT elevating in 1–2ULN in immune clearance had low levels of ALT. Therefore, we need a suitable animal model for acute exacerbation of CHB to study serial intrahepatic immunologic profiles and test any therapeutic implications of the identified cytokine targets. At the same time, the randomized controlled trials with larger samples are required to further resolve these issues in the future.

In conclusion, our data show that postpartum ALT abnormalities were associated with IL-10 elevation .IL-10 may be involved in the process of postpartum hepatitis flares. Further studies are needed to explore the mechanism and treatment values of IL-10 in HBeAg positive postpartum patients with high viremia.

Author contributions

Conceptualization: Ming Wang, Yun-xia Zhu.

Data curation: Ming Wang, Yun-xia Zhu.

Formal analysis: Ming Wang.

Funding acquisition: Ming Wang, Hua Zhang, Yun-xia Zhu.

Investigation: Ming Wang, Ying Hou, Bo Yang, Ping Yang, Yun-xia Zhu.

Methodology: Ming Wang.

Resources: Hua Zhang, Yun-xia Zhu.

Supervision: Yun-xia Zhu.

Writing – original draft: Ming Wang, Shi-hui Meng.

Writing – review & editing: Ming Wang, Shi-hui Meng, Yun-xia Zhu.

Supplementary Material

Supplemental Digital Content
medi-98-e17969-s001.doc (35.5KB, doc)

Supplementary Material

Supplemental Digital Content
medi-98-e17969-s002.doc (32.5KB, doc)

Supplementary Material

Supplemental Digital Content

Footnotes

Abbreviations: ALT = alanine aminotransferase, CHB = chronic hepatitis B, G-CSF = granulocyte colony stimulating factor, HBeAg = hepatitis B e-antigen, HBIg = hepatitis B immune globulin, HBsAg = hepatitis B surface antigen, HBV = hepatitis B virus, IL = interleukin, INF-γ = interferon-γ, LdT = telbivudine, MTCT = mother-to-child transmission, TDF = tenofovir disoproxil fumarate, TNF-α = tumor necrosis factor-α, ULN = upper limits normal.

How to cite this article: Wang M, Hou Y, Meng SH, Yang B, Yang P, Zhang H, Zhu Y. Abnormal IL-10 levels were related to alanine aminotransferase abnormalities during postpartum in HBeAg positive women with chronic hepatitis B. Medicine. 2019;98:46(e17969).

This study is supported by a research grant from Major project of Beijing Municipal Science and Technology Commission (grant number D161100002716004) and National Science and Technology Major Project (grant number 2017ZX10201201-001-009).

The authors have no conflicts of interest to disclose.

Supplemental Digital Content is available for this article.

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