Molecular adjuvant interleukin-33 enhances the antifertility effect of Lagurus lagurus zona pellucida 3 DNA vaccine administered by the mucosal route

Abstract

It has been shown that cytokines can act as molecular adjuvant to enhance the immune response induced by DNA vaccines, but it is unknown whether interleukin 33 (IL-33) can enhance the immunocontraceptive effect induced by DNA vaccines. In the present study, we explored the effects of murine IL-33 on infertility induced by Lagurus lagurus zona pellucida 3 (Lzp3) contraceptive DNA vaccine administered by the mucosal route. Plasmid pcD-Lzp3 and plasmid pcD-mIL-33 were encapsulated with chitosan to generate the nanoparticle chi-(pcD-Lzp3+pcD-mIL-33) as the DNA vaccine. Sixty female ICR mice, divided into 5 groups (n=12/group), were intranasally immunized on days 0, 14, 28, and 42. After intranasal immunization, the anti-LZP3-specific IgG in serum and IgA in vaginal secretions and feces were determined by ELISA. The results showed that chi-(pcD-Lzp3+pcD-mIL-33) co-immunization induced the highest levels of serum IgG, secreted mucosal IgA, and T cell proliferation. Importantly, mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) had the lowest birth rate and mean litter size, which correlated with high levels of antibodies. Ovaries from infertile female mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) showed abnormal development of ovarian follicles, indicated by atretic follicles and loss of oocytes. Our results demonstrated that intranasal delivery of the molecular adjuvant mIL-33 with chi-pcD-Lzp3significantly increased infertility by enhancing both systemic and mucosal immune responses. Therefore, chi-(pcD-Lzp3+pcD-mIL-33) co-immunization could be a strategy for controlling the population of wild animal pests.

DNA immunocontraceptive vaccine; Interleukin 33; Intranasal co-immunization; Antifertility effect; Anti-LZP3-specific IgG; Lagurus lagurus

Introduction

Immunocontraception prevents pregnancy or oocyte fertilization by immunological mechanisms (¹-³). The potential of immunocontraceptive vaccines to control the population of pest animals and wildlife such as foxes, mice, rabbits, African elephants, and white-tailed deer has been investigated (⁴-⁶). Mammalian zona pellucida glycoprotein (ZP) is made up of three sulfated glycoproteins (ZP1, ZP2, ZP3 or ZPA, ZPB, ZPC) that surround the oocyte (⁷). ZP3 glycoprotein, a primary sperm receptor, plays a critical role in specific sperm-oocyte combining and triggers the acrosome reaction (⁸,⁹). It has been regarded as a promising target antigen for developing an immunocontraceptive vaccine because ZP3 antibodies (Abs) can block sperm-oocyte binding (⁹-¹¹).

It has been shown that inoculation of murine cytomegalovirus-expressing mouse ZP3 (mZP3) (²) or purified mZP3 protein expressed by vaccinia virus (¹²) induces an anti-ZP3 immune response and results in a strong immunocontraceptive effect in immunized mice. Except for the direct effects of ZP3 Abs blocking the sperm binding site, some studies showed that ovarian pathological features characterized by depletion of primordial follicles and loss of follicles might cause the infertility induced by ZP3 protein vaccination (⁷,¹³). Accumulated evidence indicates that both T cell and Ab-mediated reactions could cause ovarian pathology (¹⁴-¹⁶). For humans, a safe immunocontraceptive vaccine should not induce ovarian pathology. A number of research groups focused their investigations on developing a safe and effective immunocontraceptive vaccine (¹⁰,¹⁷,¹⁸). However, for wildlife pests such as Lagurus lagurus (a wild pest in the Xinjiang desert grassland, in Northwest China), immunocontraceptive efficiency should be the first issue of concern. Therefore, we tried to develop an effective DNA vaccine expressing LZP3 to decrease the fertility of L. lagurus. DNA vaccines can induce both cellular and humoral responses, but the level of immune response needs to be further improved, especially humoral responses.

The signaling of interleukin 33 (IL-33), a novel cytokine of the IL-1 family, and its receptor ST2 promotes generation of proinflammatory cytokines, chemokines, and Th2-associated cytokines in many cells of the immune system such as Th2 lymphocytes, basophils, eosinophils, mast cells, and natural killer cells (¹⁹,²⁰). IL-33 has strong immunomodulatory functions and predominantly induces Th2 immune responses (²¹,²²) by activating dendritic cells (²³). The Th2 immune response is important for induction of Ab production because Th2 cells effectively activate B cells to secrete Abs (²⁴). Th2 immune responses to ZP3 antigens also play a role in autoimmune infertility caused by immunization with ZP3 proteins (¹²). Therefore, we chose IL-33 as a molecular adjuvant for our DNA vaccine.

Conventional vaccine delivery technologies are based on injection into the body of a mixture of protective components with an immunostimulatory agent (²⁵). Direct injection of zona pellucida antigens into the body is not feasible for controlling the overpopulation of widely distributed pest animals (²⁶). Mucosal vaccination has the advantage of needle-free administration, induces both systemic and mucosal immune responses, and can be used for mass vaccination (²⁵). Our previous studies showed that nasal immunization induced both IgA and IgG Ab responses to mZP3 in mouse models (²⁷,²⁸). In order to protect DNA from degradation, chitosan, a biodegradable cationic polysaccharide, was used to encapsulate the plasmid DNA as in our previous studies (¹⁴,²⁷).

In this study, LZP3 DNA vaccine (pcD-Lzp3) and a molecular adjuvantMus musculus IL-33 (pcD-mIL-33) were encapsulated with chitosan and delivered intranasally into ICR mice, an outbred Swiss-derived model. The results showed that mice intranasally co-immunized with chitosan (chi)-(pcD-Lzp3+pcD-mIL-33) produced significantly higher levels of systemic and mucosal immune responses than mice immunized with chi-pcD-Lzp3 alone and decreased the birth rate, suggesting that IL-33 is a good candidate for developing an immunocontraceptive DNA vaccine for L. lagurus.

Material and Methods

Animals

Female ICR mice (6-8 weeks old) were purchased from the Center for Disease Control and Prevention (Xinjiang, China). Animal experimental procedures were in compliance with regulations issued by the Science and Technology Department [approval number SCXK (Xin) 2003-0002] of Xinjiang Uygur Autonomous Region, China.

LZP3 antigen and plasmids

The core coding region of the L. lagurus ZP3 gene (Lzp3, GenBank No. AF515621) was cloned into pGEX-4T-1 to generate pGEX-4T-1-Lzp3 plasmids, which were expressed inEscherichia coli BL21(DE3) as a GST-LZP3 fusion protein. GST-LZP3 was purified and quantified using a Bradford micro-assay kit (Tiangen, China), and was used as a specific antigen in ELISA or T-cell proliferation assays. Lzp3 was inserted into the eukaryotic expression plasmid pcDNA3.0 to produce a pcD-Lzp3 construct, which was used as the DNA vaccine. mIL-33 encoding the open reading frame of M. musculus IL-33 was inserted into the pcDNA3.0 plasmid to yield a pcD-mIL-33 plasmid that was used as the molecular adjuvant. pcD-mIL-33 was prepared on a large scale and transfected into mouse hepatocytes by a hydrodynamic-based transfection method to detect the expression of mIL-33 (²⁹). Briefly, 37.5 µg (12.5 μg/mL) plasmid was injected via the tail vein using a 21-gauge needle syringe. The plasmid solution injection was completed within 8-10 s and did not exceed 8-10% body weight according to the age and weight of mice. Total RNA was extracted from hepatocytes 8 h after injection, and the expression of the target gene was assayed by RT-PCR.

Preparation of chitosan-DNA complex nanoparticles

Chitosan (170 kD, 85% deacetylated) was purchased from Xindie Chitin Co., Ltd., China. Chitosan-DNA nanoparticles were prepared as described previously (¹⁴,²⁷). In brief, chitosan was dissolved completely in 1% acetic acid, then 0.14% chitosan solution (w/v) in 0.1 M sodium acetate buffer, pH 5.7, and 100 μg/mL plasmid (pcD-Lzp3, pcD-mIL-33, or pcDNA3) solution in 0.2 M sodium sulfate were incubated at 55°C for 30 min separately, then were mixed together quickly and shaken vigorously for 60 s. The DNA plasmids were encapsulated with chitosan in a 1:7 ratio. The resulting nanoparticles were named chi-pcDNA3, chi-pcD-Lzp3, and chi-pcD-mIL-33, respectively. Equal amounts of pcD-Lzp3 and pcD-mIL-33 were encapsulated together with chitosan to generate the nanoparticle chi-(pcD-Lzp3+pcD-mIL-33). The mixture was kept at 4°C for 30 min, then centrifuged at 10,000g at 4°C for 20 min. Pellets were resuspended in 0.9% sterile saline, and the final concentration of plasmid DNA in the chitosan-DNA complex was 2.5 μg/μL.

Examination of chitosan-DNA nanoparticles

For scanning electron microscopy observation, 20 μL chitosan-DNA nanoparticle solution was pipetted onto a glass slide and sprayed with silver powder after being dried for 30 min. The surface of the chitosan-DNA nanoparticles was observed using scanning electron microscopy.

The protective effect of chitosan against nuclease degradation of DNA plasmids was checked by gel electrophoresis. The chitosan-coated plasmids and the corresponding naked plasmids (3.4 μL) were separately digested with 0.3 μL 5 U/μL DNase I (Takara, China) at 37°C for 30 min in a 20-μL digestion system. Two microliters of 6× loading buffer was added to deactivate DNase I after each reaction. The protective effect of chitosan on DNA was detected by 0.7% agarose gel electrophoresis.

Intranasal immunization with chitosan-DNA nanoparticles

Sixty ICR female mice were randomly divided into 5 groups (n=12/group). The five groups were randomly administered chi-(pcD-Lzp3+pcD-mIL-33), chi-pcD-Lzp3, chi-pcD-mIL-33, chi-pcDNA3, and chitosan. Inoculation was conducted intranasally on days 0, 14, 28, and 42 by dropping 40 μL of the chitosan-DNA nanoparticle solution (containing 100 μg plasmid DNA) into a nasal cavity with a Gilson pipette. In the co-immunization group, each mouse was inoculated with a total of 80 μL chi-(pcD-Lzp3+pcD-mIL-33) nanoparticle solution (containing 100 μg pcD-Lzp3 and 100 μg pcD-mIL-33). In the blank control group, each mouse received 40 μL chitosan solution.

Sample collection

Serum was collected from mice at 2, 4, 6, and 8 weeks after the first immunization and stored at −20°C until ELISA detection for IgG, and at the same time vaginal washings and fecal extracts were collected to measure secretory IgA (sIgA). The vaginal washings were obtained by washing the mouse's vaginal cavity with 150 μL sterile PBS containing 1% bovine serum albumin (BSA-PBS) nine times with a Gilson pipette. The vaginal washing was centrifuged at 10,000 g at 4°C for 20 min. The supernatant was collected, 10 mM protease inhibitor phenylmethylsulfonyl fluoride (PMSF) was added, and then it was stored at −20°C. The fecal sample was dissolved in 1 mL PBS at a final concentration of 0.1 g/mL and kept at 4°C for 2 h, and then vigorously shaken for 5 min. The fecal sample was centrifuged at 10,000 g for 20 min at 4°C, and the supernatant was collected and detected by ELISA.

Assessment of specific IgG and sIgA responses

The levels of anti-LZP3 Abs in the serum samples, vaginal washings, and fecal extracts were determined using ELISA. A 96-well microtiter plate (Jet Biofil^¯, China) was coated with 5 μg/mL recombinant LZP3 protein (in 10 mL 0.05 M bicarbonate buffer, pH 9.6) at 4°C overnight, and then was blocked with 3% BSA-PBST (PBS with 0.05% Tween 20) for 2 h at 37°C. The serum and vaginal washings were diluted at 1:100 and 1:4 in 1% BSA-PBST, respectively. One hundred microliters of serum dilution, vaginal washing dilution, or supernatant of fecal extract was added to each well and incubated at 37°C for 1 h. The plate was washed four times with 350 μL PBST with a microplate washer. After washing, 100 μL secondary, goat anti-mouse IgG conjugated with horseradish peroxidase (Southern Biotechnology Associates, USA) at a dilution of 1:8000 in 1% BSA-PBST was added to each well and incubated at 37°C for 1 h. Other secondary Ab IgA subtypes (Southern Biotechnology Associates) were diluted at 1:10,000. To display the color, 100 mg 3,3′,5,5′-tetramethylbenzidine (TMB) (Shanghai Lanji Science and Technology Development Co., Ltd., China) was dissolved in 10 mL dimethyl sulfoxide (DMSO), then 100 μL of the TMB solution and 42 μL 0.75% H₂O₂ were added to 10 mL 0.025 M phosphate-citrate buffer, and 100 μL of the resulting solution was added to each well. Finally, 50 μL 2 M H₂SO₄ was added to each well to stop the reaction. The absorbance at 450/655 nm was read with a microplate spectrophotometer (Benchmark Plus™, Bio-Rad, USA). Antibody titers were determined by the ratio of the absorbance values (postimmune/preimmune ≥2.0) with successive dilution of the serum of each sample.

T cell proliferation

On day 7 after the final immunization, spleens were collected from immunized mice. A suspension of single splenocytes was made and 1×10⁵cells/well were inoculated onto a 96-well plate in RPMI-1640 medium with 10% fetal bovine serum and stimulated in vitro by each of the following antigens: 20 μg/mL ConA as a positive control, 10 μg/mL LZP3 protein as a specific antigen, 2.0 μg/mL BSA as an irrelevant antigen, or medium. The plate was incubated with 5% CO₂ for 48 h at 37°C.

To determine lymphocyte proliferation, 20 μL MTT solution [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, 5 mg/mL in PBS, pH 7.2-7.4] was added to each well and further incubated for 4 h at 37°C. One hundred microliters of DMSO was added to each well, and the absorbance was measured at 570 nm using a microplate spectrophotometer (Benchmark Plus™, Bio-Rad). Data are reported as stimulation index, calculated as the mean absorbance of triplicate wells stimulated with an antigen, and divided by the mean absorbance of triplicate wells stimulated with the medium (A_antigen/A_control, used as control) (²⁷,²⁸).

Detection of contraceptive efficacy

Immunized ICR female mice were mated on day 7 after the last immunization with healthy fertile male ICR mice. Mating was performed by housing two immunized female mice together with a male mouse in one cage. The male and female mice were co-habited for 16 days to assess the efficacy of the contraceptive.

Histological analysis of the ovaries

Mouse ovaries were fixed in 4% paraformaldehyde buffer, dehydrated and embedded in paraffin, and subsequently sectioned at a thickness of 5 μm. The slides were stained with hematoxylin and eosin (HE), and then observed and photographed using a Leica inverted fluorescence microscope (Leica, DMI Series, Germany).

Statistical analysis

Data are reported as means±SE, and were analyzed using the one-sided Studentt-test and one-way analysis of variance with the GraphPad Prism 4 software. A value of P<0.05 was considered to be statistically significant.

Results

Characterization of chitosan-DNA nanoparticles

The morphology of the chitosan-DNA nanoparticles was observed with scanning electron microscopy (Figure 1). The size of chitosan-DNA nanoparticles was approximately 100-1000 nm. The protective effect of nanoparticles was detected using DNase I digestion. The nanoparticles completely protected DNA plasmids from digestion by DNase I, whereas the naked DNA was completely degraded by DNase I after 30 min (Figure 2). These results show that chitosan could protect DNA vaccine from degradation.

Figure 1
Scanning electron microscope (SEM) analysis of the chitosan-encapsulated plasmid DNA. DNA plasmids were encapsulated by the chitosan at the ratio of 1:7, and the generated chitosan-DNA complexes were observed under the SEM at a magnification of 30,000×.

Figure 2
Degradation of the chitosan-DNA nanoparticles by DNase I. The chitosan-DNA nanoparticles and naked DNA plasmids were all digested with or without DNase I (RNase free, 40 U/µL) at 37°C for 30 min. The resulting products were analyzed by agarose gel electrophoresis.Lane 1, chitosan-DNA nanoparticles were digested without DNase I; lane 2, naked DNA plasmids were digested without DNase I; lane 3, chitosan-DNA nanoparticles were digested by DNase I; lane 4, naked DNA plasmids were digested by DNase I.

Transcription expression of mIL-33 plasmid in mouse hepatocytes

In order to confirm the expression of mIL-33 plasmids in the eukaryotic cells, plasmid pcDNA3-mIL-33 was transfected into mouse hepatocytes. Total RNA was isolated 8 h after transfection and RT-PCR was conducted. A specific band of 801 bp was observed from the cells transfected with pcD-mIL-33, which is consistent with the size of mIL-33, whereas a similar size band was not displayed in the negative control groups (Figure 3). The results revealed that the construct encoding mIL-33 was expressed in eukaryotic cells.

Figure 3
Expression of pcDNA3-mIL-33 in mouse hepatocytes. Total RNA was extracted from mouse hepatocytes 8 h after transfection with pcDNA3-mIL-33 using the hydrodynamics-based transfection method. The templates used for RT-PCR were as follows:lane 1, distilled water as a negative control;lane 2, cDNA from hepatocytes of mouse transfected with pcDNA3 as a negative control; lane 3, RNA from hepatocytes of mouse transfected with pcDNA3-mIL-33 as a negative control; lane 4, cDNA from hepatocytes of mouse transfected with pcDNA3-mIL-33; lane 5, pcDNA3-mIL-33 plasmid served as a positive template. M1: 1500 bp DNA marker; M2: DL15,000+2000 bp DNA marker.

Systemic IgG Ab responses to different nanoparticles

To investigate whether these different nanoparticles could induce humoral immune responses, serum samples were collected on days 14, 28, 42, 56, and 70 after the first immunization, and anti-LZP3 IgG Abs were detected by ELISA. As shown inFigure 4A, the group immunized with chi-pcD-Lzp3 produced LZP3-specific IgG Abs, which were significantly higher than control groups immunized with chitosan, chi-pcDNA3, and chi-pcD-mIL-33 on days 42 and 56 (P<0.05). The level of LZP3-specific IgG Abs produced by the mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) was statistically higher than that observed in the mice immunized with chi-pcD-Lzp3 and in the control groups on days 28, 42, 56 (P<0.01) and 70 (P<0.05 vs control groups; Figure 4A). LZP3-specific IgG Abs were detected as early as 28 days in chi-(pcD-Lzp3+pcD-mIL-33) co-immunized mice, suggesting that chi-(pcD-Lzp3+pcD-mIL-33) co-immunization not only enhanced the level of IgG Ab but also quickly induced Ab production. The level of Abs reached the maximum on day 42. The highest IgG titer of the group co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) was 4000 on day 42 (P<0.01 vs chi-pcD-Lzp3 and control groups; P<0.05 vs control groups; Figure 4B). Importantly, we analyzed the level of IgG Ab in infertile and fertile mice after mating. The levels of IgG Abs in infertile mice were significantly higher than those in fertile mice in the co-immunized group (P<0.01; Figure 5), suggesting that infertility was correlated with the higher level of Abs. The results showed that mIL-33 as a molecular adjuvant for pcD-Lzp3 DNA vaccine could enhance systemic Ab responses against ZP3 through mucosal immunization.

Figure 4
Serum anti-LZP3 IgG of ICR mice immunized intranasally with different chitosan-DNA nanoparticles. Serum samples were collected from mice (n=12/group) immunized with different nanoparticles on days (d) 14, 28, 42, 56, and 70 after the 1st immunization. A, Anti-LZP3 IgG levels of serum (diluted at 1:100) were detected by ELISA on days 14, 28, 42, 56, and 70. ⁺P<0.05, compared to the control groups immunized with chitosan, chi-pcDNA3 and chi-pcD-mIL-33; **P<0.01, chi-(pcD-Lzp3+pcD-mIL-33) group compared to the chi-pcD-Lzp3 group and the control groups (one-way ANOVA). B, Serum anti-LZP3 IgG levels (diluted from 1:100 to 1:4000) were assessed by ELISA on day 42 after the 1st immunization. ⁺P<0.05, chi-pcD-Lzp3 group compared to the control groups; **P<0.01, chi-(pcD-Lzp3+pcD-mIL-33) group compared to the chi-pcD-Lzp3 group and the control groups (one-way ANOVA).

Figure 5
Anti-LZP3 IgG levels in serum of fertile and infertile mice. Anti-LZP3 IgG levels in serum of fertile and infertile mice (n=8/group) were detected by ELISA on day 56 after the 1st immunization. *P<0.01, IgG levels in infertile mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) compared to fertile mice (one-sided Studentt-test).

Mucosal IgA responses

After testing the systemic IgG Ab responses, we detected a mucosal response, antigen-specific sIgA, in the vaginal washes and fecal extracts by ELISA. Chi-(pcD-Lzp3+pcD-mIL-33) co-immunization quickly induced high levels of LZP3-specific sIgA in the vaginal washes and reached peak responses on day 28 after the first immunization. The sIgA levels in response to co-immunization were statistically higher than those in mice immunized with chi-pcD-Lzp3 and the control groups on days 28, 42, and 70. On day 56, both chi-(pcD-Lzp3+pcD-mIL-33) and chi-pcD-Lzp3 induced higher sIgA levels than control groups, but the sIgA level of chi-pcD-Lzp3 quickly decreased on day 70 (Figure 6A). Both chi-(pcD-Lzp3+pcD-mIL-33) and chi-pcD-Lzp3 induced LZP3-specific sIgA in fecal extracts on day 28, and the level of sIgA induced by chi-(pcD-Lzp3+pcD-mIL-33) was significantly higher than that induced by chi-pcD-Lzp3 and the control groups (P<0.05 vs chi-pcD-Lzp3and control groups; Figure 6B). LZP3-specific sIgA in mice immunized with chi-pcD-Lzp3decreased to basal levels on day 42, but a high level of LZP3-specific sIgA in mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) remained on day 42. These results suggest that mIL-33 not only increases the level of sIgA induced by LZP3 DNA vaccine but also enhances the longevity of sIgA.

Figure 6
SIgA levels from vaginal washes and fecal samples of ICR mice immunized intranasally with different chitosan-DNA nanoparticles. Vaginal washes were collected from each immunized mouse (n=12/group). Fecal samples were collected from immunized mice (n=12/group). LZP3-specific sIgA (secretory IgA) antibodies in vaginal washes (diluted at 1:4) on days (d) 28, 42, 56, and 70 (A) and fecal samples on days 28 and 42 (B) after the 1st immunization were determined by ELISA. ⁺P<0.05, IgA levels in mice immunized with chi-pcD-Lzp3 compared to control group mice immunized with chitosan, chi-pcDNA3 and chi-pcD-mIL-33 (one-way ANOVA). *P<0.05, IgA levels in mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) compared to mice immunized with chi-pcD-Lzp3 and the control groups (one-way ANOVA).

T cell proliferation in vitro

The above results show that mIL-33 enhanced systemic and mucosal Ab responses induced by LZP3 DNA vaccine. We next examined whether mIL-33 enhanced cellular responses. T cell proliferation in vitro was assessed by the MTT method. The level of T cell proliferation induced by chi-(pcD-Lzp3+pcD-mIL-33) was significantly higher than that of other groups (P<0.05; Figure 7). The level of T cell proliferation induced by chi-pcD-Lzp3 was somewhat higher than that of the control groups but was not significantly different. The results indicated that IL-33 as a mucosal adjuvant also enhanced antigen-specific cellular immune responses.

Figure 7
T cell proliferation in spleens of ICR mice immunized intranasally with different chitosan-DNA nanoparticles. Spleens were isolated from the vaccinated mice (n=3/group) on day 7 after the last immunization. Single cell suspensions were prepared and stimulated in vitro with LZP3 protein, BSA and ConA, separately. T cell proliferation was determined by the MTT colorimetric method.⁺P<0.05, stimulation index of mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) compared to mice immunized with chitosan, chi-pcDNA3, and chi-pcD-mIL-33 (one-way ANOVA).

Analysis of antifertility

To detect the antifertility effect of the mice immunized with different nanoparticles, the rate of fertility was recorded. The results showed that mice of the co-immunized group had the lowest birth rate and mean litter size compared with the other groups. Three of 8 female mice in the co-immunized group were infertile, the other 5 females had 54 pups in total, and the average litter size for the entire group was 6.75 pups, that is, significantly lower than that of other groups (Table 1). Only one mouse in the group immunized with chi-pcD-Lzp3 was infertile, and the average litter size was 9.25. All females in other control groups were fertile. These results showed that the fertility of mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) by intranasal delivery was reduced.

Ovarian pathology

Ovaries were collected from immunized mice 6 weeks after mating. Ovarian slides were prepared and stained with HE. The results indicated that the fertile mice immunized with chi-(pcD-Lzp3+pcD-mIL-33) or chi-pcD-Lzp3 or other control groups had normal follicles in numbers and in morphology with primordial, primary, secondary, tertiary, and mature follicles (Figure 8A-F). The mature follicles contained oocytes surrounded by a single layer of granulosa cells. However, the infertile mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) showed aberrant development of ovarian follicles (Figure 8E1), where secondary follicles and tertiary follicles were absent and the number of primary follicles was reduced. The results suggest that T cell responses induced by chi-(pcD-Lzp3+pcD-mIL-33) co-immunization may cause an abnormal morphological structure of the ovary that may be correlated with lower fertility.

Figure 8
Histological examination of ovarian sections of the ICR mice immunized intranasally with different chitosan-DNA nanoparticles. Ovaries were collected from fertile and infertile mice (n=6/group) on day 49 after final immunization. Ovarian sections were stained with hematoxylin and eosin and photographs (100X) were taken under a microscope. Ovaries were collected from naive mice (A) or mice immunized with chitosan (B), chi-pcDNA3 (C), chi-pcD-Lzp3(D), chi-(pcD-Lzp3+pcD-mIL-33) (E, E1) and chi-pcD-mIL-33 (F). Black arrows indicate normal mature ovarian follicles; white arrows indicate immature ovarian follicles; white arrowheads indicate tertiary follicles; black arrowheads indicate atrophic follicles; CL: corpora lutea; St: stroma.

Discussion

In order to enhance the immunogenicity of DNA vaccines, many materials, such as liposomes and poly(DL-lactide-co-glycolic acid) microspheres, have been tested for protecting the DNA from degradation (³⁰,³¹). In the present study, the chitosan-DNA nanoparticles displayed resistance against DNase I degradation (Figure 2). This could result in that a greater amount of plasmid DNA in the chitosan-DNA complex was not degraded, more DNA would be used for transcription, leading to the formation of a greater amount of antigenic protein and the generation of a better immune response (³²). Chitosan also has an immune-stimulating activity, including recruitment and activation of macrophages and polymorphonuclear cells, and enhancing the cytotoxic T cell response (³³). Chitosan-DNA nanoparticles can induce mucosal immunity and produce sIgA (³³-³⁵).

Cytokines have been used as mucosal adjuvants to overcome the mucosal tolerance and promote IgA secretion because of their pleiotropic functions (³⁶). Cytokines can enhance both mucosal and systemic immunities. Intranasal co-immunization of mice with IL-15-expressing DNA constructs with foot and mouth disease virus DNA vaccine increased the levels of both IgG and sIgA (³⁶). IL-33 administration could induce production of IgA and IgG by increasing the production of Th2-associated cytokines, IL-5 and IL-13 (²²), or activation of mast cells (³⁷). Consistent with that, we also observed that IL-33 enhanced not only the level of systemic IgG but also mucosal sIgA in the vaginal tract and intestine (Figures 4A, 6A and B). Interestingly, nasal immunization at one local IgA inductive site always induced specific immunity responses at distant mucosal effector sites through the common mucosal immune system (³³); therefore, nasal immunization could produce a strong genital-vaginal mucosal immune response and mucosal IgA antibody (³⁸). Our study showed that co-immunization with chi-(pcD-Lzp3+pcD-mIL-33) in the nasal cavity could also elicit IgA responses in the genital tract and intestine through the common mucosal immune system. All this evidence has demonstrated that intranasal immunization is an effective method to generate specific mucosal immune responses in the female reproductive tract and that IL-33 is a good molecular adjuvant for intranasal administration.

IgG Abs against ZP3 in the circulation are very important to infertility, because the Abs can infiltrate through ovarian follicles and bind to ZP to block sperm-oocyte binding in vivo (¹¹). In several studies, high titers of ZP-specific total IgG Abs are associated with infertility in mice immunized with the recombinant ZP3 protein or ZP3 peptides (¹²,¹⁸,³⁹). Consistent with those studies, we also demonstrated that the higher level of total IgG Abs was correlated with infertility in mice in the group co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) (Figure 5). Furthermore, chi-(pcD-Lzp3+pcD-mIL-33) co-immunization also induced high levels of mucosal sIgA, which may be also correlated with decreased fertility. The mean litter size and birth rate of mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33) were significantly reduced compared with control groups.

Anti-LZP3-specific Abs may lead to abnormal development of ovaries. Calongos et al. (⁴⁰) and Lloyd et al. (¹⁶) found that anti-ZP Abs were detrimental to normal folliculogenesis and oocyte development. Anti-ZP Abs may give rise to follicle loss and premature ovarian failure because they impair zona pellucida formation in developing follicles and formation of gap junctions between the oocyte and granulosa cells (¹⁶,⁴⁰). Some reports suggested that anti-ZP Abs may induce infertility of immunized mice via two mechanisms, one disrupting ZP formation and oocyte development and the other blocking sperm-oocyte binding and oocyte fertilization. The degree to which these two mechanisms each bear responsibility for infertility may rely on the Ab titer and the interval since the beginning of the response (¹⁶). Our results showed that chi-(pcD-Lzp3+pcD-mIL-33) co-immunization induced significantly higher levels of Abs in infertile mice than in fertile mice, suggesting that the infertility may be due to the Abs blocking sperm-oocyte binding. We also observed abnormal development of follicles in infertile mice co-immunized with chi-(pcD-Lzp3+pcD-mIL-33), which may be correlated with the high level of T cell proliferation, and the abnormal development of follicles may also contribute to infertility.

Taken together, our results show that IL-33 is a good molecular adjuvant to enhance systemic and mucosal Ab responses and cellular responses induced by LZP3 DNA vaccine. Importantly, chi-(pcD-Lzp3+pcD-mIL-33) co-immunization significantly increased infertility. We provide a potential strategy to control the population of wild animal pests.

We would like to thank Dr. Ji Ma, Dr. Jinyao Li and Ms. Jiayinaguli Zhumabai for the critical reading and for revising the manuscript. We also thank Mr. Yonghai Liang for his technical support. Research supported by the Research Starting Foundation for Doctors of Xinjiang University (#BS120112) to Dr. Y.X. Tu, and the Natural Science Foundation of China (#30760136) to F.C. Zhang.

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• First published online December 2, 2013.

Publication Dates

• Publication in this collection
  10 Dec 2013
• Date of issue
  Dec 2013

History

• Received
  15 Apr 2013
• Accepted
  23 July 2013