Contribution of sex‑based immunological differences to the enhanced immune response in female mice following vaccination with hepatitis B vaccine

  • Authors:
    • Meng Li
    • Yuwei Zhao
    • Xue Chen
    • Xuemei Fu
    • Wen Li
    • Humin Liu
    • Yufang Dong
    • Chuanyao Liu
    • Xiao Zhang
    • Li Shen
    • Bing Li
    • Yaomei Tian
  • View Affiliations

  • Published online on: May 10, 2019     https://doi.org/10.3892/mmr.2019.10231
  • Pages: 103-110
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Abstract

Hepatitis B virus (HBV) vaccination is regarded as the most economical and effective method for the prevention and control of HBV infection, a major global health problem. Previous studies have suggested that there may be sex‑specific differences regarding the immune response to the HBV vaccine in humans; however, the mechanisms associated with these sex‑specific differences are yet to be elucidated. In the present study, sex‑based immunological differences in mice following HBV vaccination were investigated to determine the mechanisms underlying sexual dimorphism, with the aim of identifying potential targets for clinical intervention. Balb/c mice (n=6) were vaccinated intramuscularly on 3 different days (days 0, 14 and 28) with the HBV vaccine. Sera were analyzed via ELISA for the presence of HBV surface antigen (HBsAg)‑specific immunoglobulin G (IgG), and of different IgG subtypes, 3 weeks following the third injection. Enzyme‑linked immunosorbent spot assays were conducted to determine interleukin‑4/interferon‑γ secretion. Immunological memory stimulated by the vaccine was detected via flow cytometry analysis and ELISA 1 week following the booster immunization. The seroconversion of the treated female group was higher compared with the male group at one week following the second vaccination. Female mice exhibited significantly increased HBsAg antibody titers compared with males at 1‑5 weeks following the third vaccination. Sera obtained from vaccinated female mice exhibited markedly increased titers of IgG1 and IgG2b compared with those from male mice. Furthermore, female mice exhibited elevated cytotoxic T lymphocyte responses and immune memory. Collectively, the results of the present study indicated that sex‑based immunological differences affected the dynamics and characteristics of the immune response in mice immunized with the HBV vaccine.

Introduction

Hepatitis B virus (HBV) infection is a global health problem, particularly in Southeast Asia and Africa (1). An estimated ~260 million individuals are chronic carriers, serving as the main reservoir for continued HBV transmission (24). Almost 25% of carriers develop serious liver diseases, including cirrhosis, chronic hepatitis and primary hepatocellular carcinoma (5). It is predicted that 500,000–1.2 million individuals succumb every year from the chronic consequences of HBV infection (6); however, the prevalence of HBV infection varies markedly between different countries. For example, the incidence rate is 15–20% in Taiwanese adults, 9.8% in Egypt, 7.4% in Iran, 8.6% in Israel and 7.18% in China (7,8).

Numerous countries introduced the HBV vaccine into national routine immunization schemes of infants during the 1990s to eliminate HBV transmission and prevent HBV-associated chronic liver disease. The prevalence of HBV infection subsequently decreased in the following years, as the vaccination program was universally implemented (9). The universal HBV vaccination program for infants has been incorporated into the national immunization scheme in China since 1992 (10). Between 1992 and 2006, the surface antigen of HBV (HBsAg)-positive rate among young children in China decreased from ~10% to 2.08% (11). High titers of HBV surface antibody (anti-HBs) produced in response to the HBV vaccine were revealed to be able to effectively protect humans from infection with HBV (12). At present, HBV vaccination is regarded as the most effective and economical method for the prevention and control of HBV infection (11,13,14).

Anti-HBs levels ≥10 IU/l in response to HBV vaccination are generally regarded as seroprotective, and are considered to effectively prevent HBV infection (15); however, due to interindividual differences, 5–10% of healthy immunocompetent subjects do not elicit an antibody response (16), notably increasing the possibility of HBV infection. A large number of clinical data have revealed that males exhibit an increased risk of non-responsiveness to the HBV vaccine (1719). In addition, males are more likely than females to be HBV carriers, exhibit a notably increased mortality rate from hepatocellular carcinoma associated with HBV infection (13,14,20), and HBV infection has been observed to be sexually dimorphic in humans (14). Consistent with these differences are sex-specific differences in the antibody response following vaccination; antibody responses are more easily stimulated in females than in males (21). At present, however, the mechanism underlying sex-based differences with respect to the anti-HBV immune response remains unclear. The present study aimed to determine the immunological differences in response to the HBV vaccine between immunized female and male mice, providing a potential theoretical framework for the prevention and control of HBV infection.

Materials and methods

Mice

A total of 72 BALB/c mice (36 males and 36 females, specific pathogen-free grade; aged 4–6 weeks; 13–15 g) were purchased from Beijing Huafukang Biological Technology Co., Ltd. and housed in an aseptic environment at the Animal Center of State Key Laboratory of Biotherapy of Sichuan University for 2 weeks, with adaptive feeding prior to the start of experiment. The animals were fed with a standard laboratory chow and sterile water ad libitum. They were maintained in a controlled environment at a temperature of 20–25°C, relative humidity of 40–70%, artificially illuminated with a 12:12-h light/dark cycle and air exchanges of 10–15 times/h. The experimental protocol was approved by the Ethics Review Committee for Animal Experimentation of Chengdu Blood Center. A total of 3 cohorts of 24 mice were used during the present study; a preliminary cohort, and 2 experimental cohorts. Data from the second cohort were presented for ELISpot assays, whereas data for all other assays were generated from the third cohort.

Vaccines and immunization protocol

HBV vaccines were prepared by mixing 1 µg HBsAg (cat. no. P4875; Abnova) with 25 µg alum (cat. no. 21645-51-2; Brenntag Biosector A/S) in PBS in a total volume of 100 µl. BALB/c mice were randomly divided into four groups: Male control; female control; male treated and female treated. Treated groups (n=6) were vaccinated 3 times intramuscularly with the HBV vaccine on days 0, 14 and 28. The mice in the control groups (n=6) were treated with PBS. Blood samples were collected from the tail vein, with the exception of week 7, when blood was collected via retro-orbital sampling under 4% isoflurane to obtain sufficient blood (150–200 µl) to analyze total and subtype anti-HBs titers. Serum samples were obtained via centrifugation at 4,000 × g for 10 min at 4°C following incubation at 37°C for 2 h. Sera were analyzed using ELISA for the presence of HBsAg-specific immunoglobulin G (IgG) at weeks 1, 3, 5 and 7. Enzyme-linked immunosorbent spot (ELISpot) assays were performed to determine the secreted levels of interleukin-4 (IL-4)/interferon-γ (IFN-γ) at 1 week following the third immunization. Immunological memory stimulated by the vaccine was detected using flow cytometric analysis and ELISA at 1 week following the booster immunization (week 31 immunization; schematic of treatments in Fig. 1A).

Measurement of antibodies

HBsAg solution (100 µl) diluted in carbonate buffer to a concentration of 1 µg/ml was applied to Nunc™ MaxiSorp™ 96-well flat-bottomed ELISA plates (BioLegend, Inc.) overnight at 4°C. Following washing with 5% (v/v) Tween-20 in PBS (pH 7.2; PBST), the plates were blocked with 5% non-fat dry milk and 0.05% Tween-20 in PBS for 1 h at 37°C. The plates were subsequently incubated with 2-fold diluted serum from animals for 1 h at 37°C. The initial dilution of serum for total IgG was set at 1:2,000, whereas that of the antibody subtype was 1:100. Plates were washed 5 times with PBST and subsequently detected with horseradish peroxidase-conjugated goat anti-mouse IgG (1:3,000 dilution; cat. no. ZB-2305; Beijing Zhongshan Golden Bridge Biotechnology Co., Ltd.; OriGene Technologies, Inc.), IgG1 (cat. no. 1070-05), IgG2a (cat. no. 1080-05) or IgG2b (cat. no. 1090-05; all 1:1,000 dilution; SouthernBiotech) for 1 h at 37°C. Plates were developed using Thermo Scientific™ Pierce™ 3,3′,5,5′-tetramethylbenzidine substrate (cat. no. 34028; Pierce; Thermo Fisher Scientific, Inc.) for the peroxidase color reaction, followed by detection of the absorbance at 450 nm on an ELISA microplate reader.

Detection of seroconversion

Sera from weeks 1, 3 and 5 were diluted to 1:100 with 5% non-fat milk and 0.05% Tween-30 in PBS, and subsequently analyzed for total anti-HBs IgG, following the aforementioned ELISA protocol. The calculation formula for the cut-off value was as follows: 2.1×[A450(negative control)-A450(blank)]. When the value of A450(negative control)-A450(blank) exceeded the cutoff value, the animals were classified as being anti-HBs seropositive. The seroconversion rate was determined as the percentage of anti-HBs seropositive mice in total immunized mice.

ELISpot assay

Splenocytes were isolated from immunized mice at 1 week following the final immunization as previously described (22), and ELISpot assays were performed using the mouse IFN-γ/IL-4 Dual-Color ELISpot kit (cat. no. ELD5217; R&D Systems, Inc.). Briefly, splenocytes (5×105 cells/well) were seeded in microplates that were pre-coated with mouse IFN-γ-specific monoclonal antibody and IL-4-specific polyclonal antibody. Subsequently, cells were co-incubated with 5 µg/ml HBsAg or 1 µg/ml Concanavalin A (cat. no. 11028-71-0, Sigma-Aldrich; Merck KGaA) as a positive control at 37°C for 48 h. ELISA analysis was then conducted according to the manufacturer's protocol. The spots were counted using an ELISpot reader system (Dakewe Biotech Co., Ltd.).

Flow cytometric analysis

A total of 3 treated mice were randomly selected to measure the percentage of memory T lymphocytes. Splenocytes were isolated from the immunized mice at week 32 and adjusted to 2×106 cells/ml. Splenic lymphocyte-suspending liquid (100 µl) was added into the flow tube and centrifuged at 1,000 × g for 5 min at 4°C. The cells were blocked with 1 µl anti-mouse cluster of differentiation (CD)16/CD32 mAb (cat. no. 553141) in PBS for 5 min at 4°C. Then cells were stained with peridinin-chlorophyll protein (perCP)-cyanine 5 (cy5)-anti-mouse CD4 (cat. no. 550954), perCP-cy5-anti-mouse CD8 (cat. no. 561109), phycoerythrin-anti-mouse CD44 (cat. no. 553134) and fluorescein isothiocyanate-anti-mouse CD62L (cat. no. 561917; 1 µl of each antibody) for 30 min at 4°C. All antibodies were purchased from BD Pharmingen (BD Biosciences). Then, the cells were washed twice with PBS. Stained cells were analyzed on a BD FACSCalibur™ flow cytometer (BD Biosciences). Flow cytometric analysis was performed using NovoExpress 1.2.1 software (ACEA Biosciences, Inc.).

Statistical analysis

Statistical analysis was performed using SPSS version 13.0 software (SPSS, Inc.). All values were presented as the mean ± standard deviation. The independent-samples t-test was used for comparisons between treated groups. One-way ANOVA followed by Tukey's post hoc test was used for comparisons between multiple groups. P<0.05 was considered to indicate a statistically significant difference.

Results

Seroconversion following HBV vaccination

To investigate the seroconversion rate of anti-HBs, the prepared HBV vaccines were separately injected intramuscularly into the hind legs of female or male mice at 0, 2 and 4 weeks, and subsequently the anti-HBs titers were detected at 1, 3 and 5 weeks (Fig. 1A). No changes in the immune response were elicited by the HBV vaccine in any of the mice at 1 week following the first immunization; however, 3 of the 6 female mice generated anti-HBs 1 week following the second immunization (a seroconversion rate of 50%). Conversely, the seroconversion rate of the treated male mice group at this time point was 16.7% (Fig. 1B). A 100% seroconversion rate was observed for the two treated groups following the third immunization; however, treated female mice produced a significantly increased total anti-HBs titer compared with the treated male mice (Fig. 1C).

Detection of increased levels of anti-HBs titer in treated female mice

It was previously reported that antibody responses to HBV vaccines were typically elevated in females compared with in males, particularly in young and elderly adult populations (12). To determine the effects of sex-specific differences on the efficacy of HBV vaccines, total anti-HBs titers were evaluated at 1, 3, 5, 7, 9 and 11 weeks following the first injection (Fig. 1A). The specific anti-HBs response was elicited in all immunized mice from week 3 compared with the control group (Fig. 2). In the treated female group, anti-HBs levels peaked at week 7 with a subsequent gradual reduction by weeks 9 and 11. Immune responses to the HBV vaccine were markedly increased in the treated female group compared with the treated males during the entire course of the experiment, and were significantly increased at weeks 5, 7 and 9 (Fig. 2).

Detection of increased levels of HBsAg-specific antibody subtypes in treated female mice

To further investigate the mechanisms of humoral immunity elicited by HBV vaccines, the expression of various subtypes of anti-HBs antibody were detected at week 7. Treated female mice produced a significantly increased total anti-HBs titer compared with the treated male mice at week 7 (Fig. 3A). Additionally, it was revealed that the HBV vaccine led to a non-significant trend towards an increased HBsAg-specific IgG2a titer in treated female mice compared with treated male mice (Fig. 3C). Furthermore, serum IgG1 (7.5-fold) and IgG2b (32-fold) levels were significantly increased in the treated female group compared with the treated male group (Fig. 3B and D). Collectively, the results indicated that compared with male mice, the HBV vaccine induced an increased antibody response in female mice.

Cytotoxic T lymphocyte (CTL) responses are increased in female mice compared with male mice

To further investigate the sex-based immunological differences between the female and the male mice, the production of IFN-γ and IL-4 by HBsAg-exposed splenocytes extracted from the immunized mice was detected via ELISpot assays in vitro. The number of IL-4 spot-forming cells (SFCs; blue; Fig. 4) was significantly increased in female mice compared with the treated males. Furthermore, the secretion of IFN-γ (red SFCs) was markedly increased in treated female mice compared with treated males.

Female mice exhibit heightened immune memory compared with male mice

Memory lymphocytes capable of rapid proliferation or production of specific antibodies upon encountering HBV antigens serve an important role in suppressing HBV re-infection (23,24). To determine the extent of long-term protection against HBV, treated mice were injected with an HBV vaccine booster at week 31, and anti-HBs levels were detected one week later. A total of 3 treated mice were randomly selected to measure the percentage of memory T lymphocytes. As presented in Fig. 5A and B, treated female mice exhibited a significantly increased percentage of CD4+CD44+CD62L+ memory T cells compared with treated male mice. In addition, the anti-HBs titers in the treated female mice were significantly increased compared with the male mice (Fig. 5C).

Body weight

Age-matched Balb/c mice were randomly assigned to the aforementioned four treatment groups. Body weight was measured every week. Female and male treated mice exhibited normal body weights. There were no significant differences in body weight between the control and treated animals for either gender (Fig. 6).

Discussion

Infection with HBV, an acute and chronic communicable disease, has developed into a major global health problem (7,8,25). At present, vaccination is regarded as the most effective prevention measure against HBV infection; however, ~5–10% of healthy immunocompetent subjects are non-responsive (26). Previous studies demonstrated that the male gender was associated with increased incidence of non-response to HBV vaccination (19,25,27), whereas others indicated that there was no sex-based difference in the immune response to the HBV vaccine between males and females (28,29). To clarify the biological influences of sex on the immune response to the HBV vaccine, the present study aimed to investigate the sexual dimorphism in the immune response to HBV vaccination in mice.

In the present study, sex-specific differences in antibody responses to the HBV vaccine were reported. Female mice exhibited an increased seroconversion rate in the early immunization stages, and sustained increased humoral immunity and cellular immunity compared with male mice. In addition, female mice developed a more effective immune memory that could rapidly induce high levels of anti-HBs or activate cellular immunity to clear HBV infection. Consistent with these results, sex-specific differences in the humoral immune response were previously observed with other vaccines, such as influenza, hepatitis B and meningococcal A (27). It was reported that females mount more frequent and stronger humoral and cell-mediated immune responses to bacterial and viral vaccines compared with males (30). According to certain studies (3135), in addition to gender, the immunogenicity of the HBV vaccine was associated with age and body mass index; old age and excessive weight reduced the immune response to HBV vaccination. In the present study, mice of the same age were randomly divided into groups and body weight was measured every one week. There were no significant differences in body weight between the groups during the study period.

The results of the present study revealed that ~50% of the female mice were seropositive for anti-HBs antibody following two injections, compared with 16.7% of the male mice. Furthermore, the female mice developed more sustained, longer-lasting and significantly increased levels of anti-HBs following the second dose of HBV vaccine. The IgG2a:IgG1 antibody level ratio is frequently used to evaluate the type of T helper cell (Th) response, with a value >1 indicating a predominantly Th1 response, and a value <1 indicating a predominantly Th2 response (3638). To evaluate the type of immune response, the levels of total IgG1, IgG2a, and IgG2b were evaluated. The production of IgG1 and IgG2b antibodies in the female group was significantly increased compared with the male group, whereas no significant difference was observed between the two groups regarding IgG2a levels; however, this may be a result of the small sample size of the study (n=6), as relative IgG2a levels were notably increased in the female group compared with the male group. These findings suggested that the immune response evoked by HBV vaccine in the two treated groups was Th2-type.

The mechanisms underlying sex differences associated with antibody responses to vaccines remain unclear. It has been reported that an observed relative increase in CD4+ T cell numbers in females compared with males may partially explain the more vigorous antibody response in females (39,40). In addition, increased levels of T cell activation and proliferation were previously detected in females compared with males when cultured peripheral blood mononuclear cells were stimulated in vitro (41,42). HBV-specific CTLs and CD4+ T lymphocytes serve important roles in determining the outcome of HBV infection (43). Viral replication usually activates the CD8+ CTL response, which contributes towards the elimination of infected cells and reduced viral loads (44). Accompanying the development of the CTL response, CD4+ T cells proliferate and produce antiviral cytokines to regulate the immune response, preventing persistent infection by sustaining the CD8+ CTL function (45) or by providing signals for the induction of CD8+ T-cell memory (4649). To characterize the functional differences between the immune responses induced by HBV vaccination in mice of different sex, the production of the antiviral cytokines, IL-4 and IFN-γ, by HBsAg-exposed splenocytes from immunized mice was analyzed by an ELISpot assay. IFN-γ, predominantly secreted by HBsAg-specific CD8+ T cells, but also by HBsAg-specific Th1 CD4+ T cells, is required for the elimination of HBV infection (50,51). IL-4 produced by CD4+ Th2 cells contributes to B-cell development and the promotion of humoral responses; IL-4 was revealed to suppress the expression and replication of HBV in a hepatocellular carcinoma cell line (52). In the present study, the number of IL-4-secreting T cells was significantly increased in females compared with in males; however, the number of SFCs secreting IFN-γ in females was not significantly different compared with in males.

HBV vaccination induces the production of a high titer of antibodies and an effective CTL response with the ability to eliminate HBV in immunized subjects (53); however, HBV-specific T-cell responses have a tendency to decline, even beyond the point of detection, in the years following vaccination (54). Therefore, the induction of immunological memory is required for achieving long-term protection (54). To characterize whether there were sexual differences in immune memory, in the present study, memory T cells were detected via flow cytometric analysis. The percentage of CD4+CD44+CD62L+ memory T cells was significantly increased in treated female mice compared with treated male mice; however, the percentage of CD8+CD44+CD62L+ memory T cells was not significantly different between the two genders. Sex-dependent differences in immunological memory have also been reported in response to other vaccines (55). The anti-HBs titers in the treated female mice were increased compared with those in the treated male mice at one week following the booster injection. A limitation of the present study is that blood samples were not collected during week 31, meaning that alterations in antibody titers prior to and following the booster could not be determined.

In conclusion, the present study may improve understanding of sexual dimorphism in the immune responses to HBV vaccine. Increasing evidence has indicated that biological sex influences the immune responses to vaccination and infection; however, the biological mechanisms underpinning such differences are yet to be determined (30,56,57). Among the most well-established mechanisms for differences in immunity is the sex-hormone milieu. Therefore, further studies into the regulatory effects of sex hormones on the immune system are required.

Acknowledgements

We thank Professor Li Yang (State Key Laboratory of Biotherapy and Cancer Center, Sichuan University) for her assistance with experiments.

Funding

This work was supported by the Medical Research Program of Sichuan Medical Association (grant no. S16018).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

YT and BL made significant contributions to the design of the study, supervised the research and finalized the manuscript. ML, YZ and XC performed the majority of the in vitro studies, and all of the in vivo experiments. ML drafted the manuscript. CL and XZ contributed to the analysis and interpretation of data. XF, WL, HL, YD and LS contributed to the design and coordination of experiments. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The experimental protocol was approved by the Ethics Review Committee for Animal Experimentation of Chengdu Blood Center.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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July-2019
Volume 20 Issue 1

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Copy and paste a formatted citation
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Spandidos Publications style
Li M, Zhao Y, Chen X, Fu X, Li W, Liu H, Dong Y, Liu C, Zhang X, Shen L, Shen L, et al: Contribution of sex‑based immunological differences to the enhanced immune response in female mice following vaccination with hepatitis B vaccine. Mol Med Rep 20: 103-110, 2019
APA
Li, M., Zhao, Y., Chen, X., Fu, X., Li, W., Liu, H. ... Tian, Y. (2019). Contribution of sex‑based immunological differences to the enhanced immune response in female mice following vaccination with hepatitis B vaccine. Molecular Medicine Reports, 20, 103-110. https://doi.org/10.3892/mmr.2019.10231
MLA
Li, M., Zhao, Y., Chen, X., Fu, X., Li, W., Liu, H., Dong, Y., Liu, C., Zhang, X., Shen, L., Li, B., Tian, Y."Contribution of sex‑based immunological differences to the enhanced immune response in female mice following vaccination with hepatitis B vaccine". Molecular Medicine Reports 20.1 (2019): 103-110.
Chicago
Li, M., Zhao, Y., Chen, X., Fu, X., Li, W., Liu, H., Dong, Y., Liu, C., Zhang, X., Shen, L., Li, B., Tian, Y."Contribution of sex‑based immunological differences to the enhanced immune response in female mice following vaccination with hepatitis B vaccine". Molecular Medicine Reports 20, no. 1 (2019): 103-110. https://doi.org/10.3892/mmr.2019.10231