7 Jun 2013: Tang H, Ming Z, Liu R, Xiong T, Grevelding CG, et al. (2013) Correction: Development of Adult Worms and Granulomatous Pathology Are Collectively Regulated by T- and B-Cells in Mice Infected with Schistosoma japonicum. PLOS ONE 8(6): 10.1371/annotation/40c28bf3-6dae-4d1e-b74c-a6a8f2450a8a. https://doi.org/10.1371/annotation/40c28bf3-6dae-4d1e-b74c-a6a8f2450a8a View correction
Schistosoma blood flukes, which cause schistosomiasis affecting 200 million people in the world, are dependent on signals from host CD4+ T cells to facilitate parasite growth and development in the mammalian host and to induce Th2-biased inflammatory granulomas. B cells, however, are reported to down-regulate granulomatous pathology in schistosomiasis, but not to affect the development of blood flukes together with CD4+ T lymphocytes. Thus it is not clear whether B cells mediate parasite development, reproduction and egg granuloma formation of schistosomes without the help of CD4+ T lymphocytes. Using mice that have severe combined immunodeficiency (scid) and mice lacking T cells (nude), we found that the absence of B cells can more seriously hamper the development and paring of adult worms, but granuloma formation of Schistosoma japonicum in scid mice was not down-regulated comparing with that in nude mice. The level of IL-10 in the sera of nude mice was significantly higher than of scid mice at 43 days post infection (p.i.). Thus multiple mechanisms of immune modulation seem to be involved in parasite development and reproduction by helminth-induced regulatory B cells. Our findings have significance for understanding the molecular connections between schistosomes and T- and B-cells, indicating that more research is needed to develop efficient vaccine-based therapies for schistosomiasis.
Citation: Tang H, Ming Z, Liu R, Xiong T, Grevelding CG, Dong H, et al. (2013) Development of Adult Worms and Granulomatous Pathology Are Collectively Regulated by T- and B-Cells in Mice Infected with Schistosoma japonicum. PLoS ONE 8(1): e54432. https://doi.org/10.1371/journal.pone.0054432
Editor: Wenzhe Ho, Temple University School of Medicine, United States of America
Received: September 17, 2012; Accepted: December 11, 2012; Published: January 22, 2013
Copyright: © 2013 Tang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work is financially supported by the national natural science foundation of china awarded #30872202. http://www.nsfc.gov.cn/Portal0/default152.htm. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Schistosomes are metazoan parasites which infect more than 200 million people worldwide, and about 700 million are at risk of infection . The host-parasite relationship (between schistosomes and mammal hosts) is complex and long-lived. As the only members of the trematodes, schistosomes have evolved separate sex. Furthermore, mating is required to induce the sexual maturation of the female as a prerequisite for egg production. The latter finally leads to inflammatory processes in the gut and the liver culminating in the formation of granulomas. The traditional opinion is that parasites may damage their hosts, and the host resists against the invading parasites by its immune response. However, some studies have suggested that host factors including endocrine and immune signals can modulate parasite development and maturation , , , .
It was recently shown that schistosome co-opt CD4+ T cell–driven mechanisms to facilitate parasite development and egg excretion , , . The role of CD4+ T cells in this process may be limited to provide non-cognate help for mononuclear phagocyte function . However, schistosome development was normal in immunoglobulin heavy chain (Igh)6−/− mice only lacking B cells , . Egg granuloma formation was dependent on sensitized CD4+ T lymphocytes, with both Th1 and Th2 subsets participating in different stages during the development of the lesions , , .
In this study we investigated whether the CD4+ T lymphocyte has influence on development of S.japonicum, and whether the B lymphocyte population was responsible for modulating schistosome development and granulomatous pathology in the absence of T cells. To address this question we conducted a detailed analysis of the development of worms in the different stages post infection, characterizing besides growth and reproduction also granuloma formation in a immunodeficiency mouse model for Schistosoma japonicum infection. Parasite development was evaluated by analyzing three separate parasitological parameters: worm length; the proportion of female parasites participating in pairs; and the number of eggs deposited in the liver by each parasite pair. Worm length was used as a measure of parasite growth during the pre-patent period, whereas pairing and egg production were used to assess parasite sexual maturation and subsequent reproductive activity, respectively. To assure the absence of B or T cells, we determined the amount of specific B- and T-lymphocyte populations in peripheral blood by flow cytometry (FCM), and the presence of IL-10 in peripheral blood by ELISA. Interestingly, our data indicate for the first time that schistosomes not only take advantage from T cell immune signals, but also from B-cells to manage development.
Materials and Methods
Parasite Maintenance and Infection
Six to eight weeks old male BALB/c mice, nude mice, and scid mice in BALB/c background, originally purchased from laboratory animal center of Wuhan university, were maintained by Wuhan university center for animal experiments(WUCAE). All animals were housed under specific pathogen-free conditions in an American Association for the Accreditation of Laboratory Animal Care internationally approved facility. A minimum of 8 mice were used in each experimental group, unless otherwise indicated. Cercariae of S. japonicum (strain from Jiangsu Province, China) were shed from Oncomelania hupensis snails . Miracidia that obtained from Eggs of livers in rabbits at 45 days post infection (p.i.) infect snails after incubated for 2–4 hours, and the snails were incubated for 75 days at 25°C. Mice were infected percutaneously via the abdomen skin with 30±1 cercariae. Each strain of mice was divided into three groups. Mice were killed at days 29, 36, or 43 p.i., respectively.
Parasites were perfused in hepatic portal veins  and immediately fixed in 4% neutral buffered formaldehyde to prevent pairs from dissociating. The collected worms were counted under a dissecting microscope. All fixed worms were photographed using a LY-WN-HPCCD,5M Pixels High-Speed HPCCD-5 Color Microscope Camera connected to a Vistavision trinocular dissecting microscope at 10× magnification. Parasite length was measured in digital images using “Image-Pro Plus 5.0” software (MediaCybernetics).
Determination of Egg Production
Following perfusion, livers were collected and weighed, and the large left lobe of each liver was digested at 37°C for 3 h in 20 ml/mg of 5% potassium hydroxide (KOH). Three replicates of 0.1 ml samples were counted from each digest and the mean value determined. Egg production per schistosome pair was calculated by dividing the total number of eggs from each mouse liver by the number of parasite pairs recovered , .
Histologic Evaluation of Granuloma Formation
The remaining right liver lobe of each mouse was fixed for histological examination. Livers were fixed in 10% buffered formaldehyde, embedded in paraffin and cut into 5-µm sections. The sections were stained with hematoxylin and eosin (H&E). Representative H&E-stained liver sections from each animal were scanned under ×400 magnifications with a compound microscope. For every granuloma containing a single egg, the granuloma size was determined by two perpendicular diameters at the mid-transmiracidial level of the egg . Digital images were analyzed using “Image-Pro Plus 5.0” software.
For analysis of T cell activation in cells recovered from peripheral blood, expression of CD4 was examined by flow cytometry, after gating on CD3+ cells. Cells isolated from peripheral blood were surface-labeled with FITC-conjugated antibodies to CD3, and PE-conjugated antibodies to CD4 (BD Biosciences). For analysis of B- cell populations, cells were stained with FITC-conjugated anti-CD45R and PE-conjugated anti-CD45. Cells expressing CD45R were examined by flow cytometry, after gating on CD45 cells. All samples were analyzed by using a LSR II Optical Bench flow cytometer with FACSDiva (BD Biosciences) and CellQuest software (BD Biosciences).
Analysis of Cytokine Production
Cytokines were measured by ELISA using Immulon 2HB plates (Thermo) according to the manufacturerś guidelines. Capture and detection antibodies for IL-10 were purchased from R&D. Serum IL-10 was measured using an in vivo cytokine capture assay (IVCCA) as previously described . ELISA plates were washed with 0.05% Tween 20 in PBS (PBST) and blocked with 5% non-fat milk in PBST. Recombinant cytokine standards (R&D) were used to assess the quantities of cytokines in supernatants using a standard curve, with OD acquired at 450 nm in an ELISA reader.
ANOVA was applied to determine the statistical significance of differences in median values from different experimental groups. In experiments involving 3 different experimental groups, LSD and Tamhane’s multiple comparison tests were employed to evaluate differences between each pair of experimental groups. Statistical analyses were performed with PASW Statistics Version 18.0 software (SPSS Inc.). P-values of less than 0.05 were considered statistically significant. Experiments were repeated twice, with 8 animals per group.
CD4+ Lymphocytes in Peripheral Blood Facilitate the Growth of S. japonicum
To evaluate the role of CD4+ T cells in schistosome growth and reproduction, we examined the body length of sexual worms (Figure 1B) and the population of lymphocytes in nude mice that lack a thymus and in BALB/c mice as the control (Figure 1A). Analysis of peripheral lymphocyte populations by FCM revealed the lack of CD4+ T cells in nude mice compared with immunocompetent BALB/c mice. In nude mice, schistosome development was impaired relative to wild type mice that have normal CD4+ T cells, as determined by measuring the parasite sizes (Figure 1B). Furthermore, the observed differences of worm length between the above two groups were neither influenced by the time point of recovery nor by gender. The overall number of worms recovered from nude mice were less than the control group (Figure 1C), especially female worms (Figure 1B). So the pairing rates in total worms from mice were not very high and the differences were no significant between the above two groups (Figure 1C). However, with respect to the number of eggs per couple in the liver of nude mice and BALB/c mice at 29, 36, 43 p.i. (Figure 2D), none of the differences was significant. Taken together, the data suggested that CD4+ T cells have no influence on reproduction, but on the growth of S. japonicum.
(A) Flow cytometric analysis of peripheral blood CD4+ lymphocytes in scid, nude and BALB/c mice, recovered at 43 days p.i. Presented are % of cells detected in CD3 gate as a mean from one of 2 experiments with 4 mice per group. (B) Parasites were recovered from the portal tract at 29, 36, 43 days p.i., and male and female worm sizes were determined based on digital micrographs. Mean values are represented by horizontal bars. (C) Total number of worms and worm pairs in nude and BALB/c mice at 29, 36, 43 days p.i… Data are represented as median± SEM.
(A) Flow cytometric analysis of peripheral blood B lymphocytes in scid, nude and BALB/c mice; peripheral blood was recovered at 43 days p.i… Presented are, % of cells in the CD45R gate as mean from one of two experiments), with 4 mice per group. (B) Sizes of parasites from scid and nude mice were measured from digital micrographs. (C) Total number of worms and worm pairs recovered from scid, nude, or BALB/c mice were compared at 29, 36, 43 days p.i… Data are represented as median± SEM. (D) Egg production by schistosome pairs, as in C. (E) IL-10 cytokine secretions, measured by ELISA, in scid (white bars), nude (gray bar) and BALB/c (black bar) mice at 29, 36, 43 days p.i. (F) Representative micrographs of parasites recovered from BALB/c mice, nude mice, or scid mice at the time points indicated p.i. (10× magnification).
B cells Promote Schistosome Growth in the Absence of CD4+ T cells
Since non-cognate CD4+ T cells were shown to facilitate parasite development , and since CD4+ T cell-mediated granulomatous pathology in schistosomasis is downregulated by a B cell-dependent mechanism , we hypothesized that B cells may also play a role in promoting schistosome development and reproduction. To test whether B cells have similar functions as CD4+ T cells, we examined S. japonicum development also in scid mice that have normal macrophages, but lack of functional B and T lymphocytes , . Indeed, the influence on development was observed. However, the extent to which parasite growth was limited varied between the different strains. the suppression of parasite growth was most serious in scid mice, and then in nude mice. As expected, the mean length of male parasites from scid mice was significantly shorter than from nude mice at different time points (36, 43 days p.i.), but there was no significant differences of the body length of female parasites (Figure 2B). We have observed that the total number of worms and the number of worm pairs recovered from scid mice were lower than those obtained from BALB/c or nude mice perfused at different time points (29, 36, 43 days) p.i.(Figure 2C). When compared with nude mice at 36 days p.i., the infected scid mice showed significantly decreased egg numbers per pair (Figure 2D), a parameter indicative for the reproductive capacity of the parasite. Scid and nude mice were quantitatively indistinguishable in terms of tissue egg recovery at 43 days p.i., which is consistent with previous studies . Nevertheless, the decline of worm pairing led to decrease in the total number of eggs in liver, indicating that B cells exert an influence on the growth of S. japonicum during primary infection.
Because schistosome infection protected mice from anaphylaxis via IL-10-producing B cells , and since IL-10 blocked the development of resistance to re-infection with schistosome , the levels of the regulatory cytokine IL-10 were elevated in infected mice (Figure 2E). A significant decrease of worm-specific IL-10 production in scid and nude mice serum levels was determined at two time points (29 and 36 days p.i.). However, a significant decrease IL-10 serum levels was only observed in scid mice 43 days p.i., whereas no differences of IL-10 levels were found in nude mice and BALB/c mice at 43 days p.i. These data suggest that depletion of B cells lead to reduce IL-10 levels in peripheral blood, even if the hosts were stimulated by helminth.
B cells are not Indispensable in the Egg Granuloma Formation in SCID Mice
To test whether host B cells contribute to granuloma formation without Th1 and Th2 subsets participating, we examined S. japonicum-derived hepatic granuloma formation by comparatively measuring of granuloma diameters in infected scid mice, nude mice, or BALB/c mice. No typical granuloma formation was observed for any group at days 29 and 36 p.i., time points where adult worms have reached the liver and start pairing as a prerequisite for subsequent egg production. Histological examinations at day 43 p.i. showed egg granulomas, which significantly differed between the different mouse strains used. Whereas BALB/c mice exhibited multi-cellular granulomas with a large number of eosinophils and minimal hepatocyte necrosis, granulomas from nude mice as well as scid mice were of smaller size showing reduced cellular infiltrations but obvious hepatocyte necrosis in the flanking liver tissue that was not observed in BALB/c mice (Figure 3A). The nude mice and scid mice developed the diameter of the granulomas that were smaller than those in the BALB/c group by 27% and 38%, however, the granulomas diameter between nude and scid group was insignificant (P>0.05).
(A) granuloma sizes calculated from isolated granulomas at 43 days after infection calculated from three separate granulomas per individual animal. (B) a typical well-formed and multi-cellular granuloma with minimal hepatocyte necrosis (×200) includes a large number of eosinophils in BALB/c. granuloma with a much reduced cellular infiltration and obvious hepatocyte necrosis surrounding egg show the relative selective depletion of eosinophils and cellularity in nude and scid, but there is no difference significant between the two.
Within the granulomas a significant diminution in the number of eosinophils was noted in nude compared with BALB/c mice. Lymphocytes and other mononuclear cells also appeared to be decreased in these granulomas, although to a lesser degree. In addition, hepatocyte necrosis in the vicinity of eggs was obvious in nude and scid, but minimal in BALB/c mice (Figure 3B).
In this study three mouse strains with different immunogenetic background were infected with S. japonicum to study effects on schistosome development and granuloma formation in the host. We have demonstrated that T cell-deficient mice as well as animals lacking functional T and B cells negatively influenced the growth of the parasite. Furthermore, we discovered a more serious impairment of schistosome development in animals lacking functional T and B cells than in mice only deficient in T cells. Pervious studies showed that schistosomes require host CD4+ T cells for normal development , , , which also mediate egg deposition via the gut wall , . Development and sexual maturation of schistosomes were also shown to be influenced by components of the adaptive immune system . Our results from S. japonicum infection in immune-deficient hosts are in agreement with previous studies suggesting that the growth of this parasite is influenced by immune signals. However, Unlike pervious researches , , we have observed that parasite development significantly differed between nude and BALB/c mice at 36 and 43 days p.i. The most likely explanation lies in a source of hosts and S. Japonicum that different sources host’s thymus glands have different immunological reactions to infection of pathogens, and development degree of different origins cercaria is different in same host. Our data indicate that CD4+ T cells are the critical immune element for normal S.japonicum development, and the absence of CD4+ T cells impairs the growth of this parasite in mice.
It was showed that CD4+ T cells had no effect on reproduction of worms. parameters of pairing and egg production of worms were no obvious differences in nude and BALB/c mice, even if eggs each pair were lower in nude mice than in normal control group at 29 and 36 days p.i. It indicated that CD4+ T cells only involved in the regulation of parasite growth. some researches showed that adoptive transfer of activated T-cells into scid mice were not sufficient to restore schistosomes eggs per pair to normal levels  and no defect in parasite paring were reported , which indicated that activated T cells did not directly influence the reproduction of blood fluke. We conclude that CD4+ T cells will only facilitate schistosome growth but not to affect schistosome reproduction including paring and egg production.
Someone thought that B cells, as the sentinels of the adaptive immune system, are not responsible for modulating schistosome development . Nevertheless, in our investigation, schistosome development, such as male worms growth, had more inhibition in sicd mice than nude mice, revealing that B cells are important for parasite development without CD4+ T lymphocytes in the host. Our data demonstrate that the absence of T or B cells not only impairs schistosome growth, but also inhibits parasite paring. Together with previous finding that adoptive transfer of wild-type CD4+ T cells into RAG-1−/− animals was sufficient to restore S. japonicum development to normal levels  and schistosomes do not respond directly to CD4+ T cells, as their absence can be bypassed completely by direct stimulation of innate immune responses ., our study implicate that B cells possibly are a by-pass or backup of CD4+ T lymphocyte regulation in the worm development. In normal circumstance, schistosome development have been played a major role by CD4+ T lymphocytes. In the absence of T cells, B cells are activated by helminth infection and produce cytokines to regulate helminth development. In support of this, IL-10-producing Bregs can also be activated by T-cell-independent stimuli, particularly TLR ligands . Thus, it is tempting to speculate that helminths may be able to induce the activity of regulatory B cells . Furthermore, in response to many stimuli, including CD40 ligation, Be-1, Be-2 cells and human peripheral blood B cells produce IL-10 make IL-10 , . For example, S. mansoni-induced regulatory B cells can attenuate allergic disease through an IL-10-dependent mechanism , , . S. mansoni infection promotes the expansion of peritoneal B1 cells and splenic B cells, and egg-derived oligosaccharides promote B cell proliferation and IL-10 production , . In this study we also measure the level of IL-10 in the peripheral blood of infected mice. Our findings correspond to results of previous studies where IL-10-competent B cells were the prevalent source of IL-10, but not other cytokines , suggesting that schistosome infections of mice stimulate B cells to produce IL-10, which may be involved in the regulation of parasite growth and paring.
Our experiment showed that parasite paring was inhibited in scid mice, but not in nude mice. In addition, parasite development was normal in Igh-6−/− mice lacking B cells . It showed that schistosome pairing was double modulated by both T and B cells, and one deficiency of them had no impact on schistosome pairing. They had also suggested B cells are a bypass or backup of T cells in the regulation of schistosome development. We have also observed that total number of eggs reduced in the livers of scid mice relative to nude and BALB/c mice at 29 and 36 days p.i., but there is no significant difference in eggs each pair among them. This has been interpreted to mean that the absence of B and T cells decreasing the rate of parasite pairing leads to drop total number of eggs in the livers, but not influence eggs each pair. In other words, schistosome reproduction is not significantly affected by B and T cells in the host.
The process of egg granuloma formation is dependent on sensitized CD4+ T lymphocytes. A variety of different mechanisms include cross-regulation by cytokines produced by Th1 or Th2 cells , , , , and the development of antiidiotypic Ab or T cells , . When quantitatively infected with S.japonicum, scid mice as well as nude mice displayed down-regulation of the granuloma formation typically observed in BALB/c mice. Surprisingly, this augmented pathology occurring in scid mice is different from in B cell-deficient mice or in mice by blockade of the receptor for IL-10 during chronic schistosomiasis  where granuloma volumes are significantly larger than that of the WT mice . And blockage of IL-10 in the in vitro granuloma assay lead to a significant increase in granuloma size with cells from intestinal patients but not with individuals in the acute phase or with the hepatosplenic form of schistosomiasis . However, as previously reported , , , T cell-deprived mice infected with S.japonicum develop greatly reduced egg granulomas and disseminated hepatocelluar lesions in the liver compared with that in intact control mice. Thus, these findings indicate that B cells may mediate CD4+ T cell to down-regulate the granuloma formation during chronic schistosomiasis, and this pathologic consequence is not directly influenced by B cells and IL-10 in the acute phase.
In conclusion, this study demonstrates that B cells and CD4+ T lymphocytes cooperatively facilitate development of blood flukes in mice. Furthermore, schistosome development is hampered more seriously in the mice lacking T and B cells mice than in the mice lacking T cells alone. As a regulatory mechanism with a bypass or backup, B cells and T cells double improve schistosome development. However, B cells contributing to the regulation of granulomatous pathology caused by schistosome infection seem to depend on CD4+ T lymphocytes. Thus, multiple mechanisms of immune modulation involving in parasite development by helminth-induced regulatory B cells are likely to exist.
The helpful comments of three anonymous reviewers and the Editor (Wenzhe Ho) are sincerely appreciated. We thank Laying Cheng and Jing Zhang for professional assistance, Ming Guo and Xin Wang for flow cytometry.
Conceived and designed the experiments: HBT HFD MSJ. Performed the experiments: HBT ZPM RL TX. Analyzed the data: HBT RL. Contributed reagents/materials/analysis tools: HBT RL. Wrote the paper: HBT RL CGG MSJ.
- 1. Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J (2006) Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect Dis 6: 411–425.
- 2. Harrison RA, Doenhoff MJ (1983) retarded development of schistosome mansoni in immunosuppressed mice. Parasitology 86: 429–438.
- 3. Amiri P, Locksley RM, Parslow TG, Sadick M, Rector E, et al. (1992) Tumour necrosis factor alpha restores granulomas and induces parasite egg-laying in schistosome-infected SCID mice [see comments]. Nature 356: 604–607.
- 4. Blank RB, Lamb EW, Tocheva AS, Crow ET, Lim KC, et al. (2006) The Common gamma Chain Cytokines Interleukin (IL)-2 and IL-7 Indirectly Modulate Blood Fluke Development via Effects on CD4+ T Cells. J Infect Dis 194: 1609–1616.
- 5. Wolowczuk I, Nutten S, Roye O, Delacre M, Capron M, et al. (1999) Infection of Mice Lacking Interleukin-7 (IL-7) Reveals an Unexpected Role for IL-7 in the Development of the Parasite Schistosoma mansoni. Infect Immun 67: 4183–4190.
- 6. Davies SJ, Grogan JL, Blank RB, Lim KC, Locksley RM, et al. (2001) Modulation of Blood Fluke Development in the Liver by Hepatic CD4+ Lymphocytes. Science 294: 1358–1361.
- 7. Cheng YL, Song WJ, Liu WQ, Lei JH, Mo HM, et al. (2008) The effects of T cell deficiency on the development of worms and granuloma formation in mice infected with Schistosoma japonicum. Parasitol Res 102: 1129–1134.
- 8. Lamb EW, Walls CD, Pesce JT, Riner DK, Maynard SK, et al. (2010) Blood fluke exploitation of non-cognate CD4+ T cell help to facilitate parasite development. Plos Pathog 6: e1000892.
- 9. Kitamura D, Roes J, Kuhn R, Rajewsky K (1991) A B cell-deficient mouse by targeted disruption of the membrane exon of the immunoglobulin μ chain gene. Nature 350: 423–426.
- 10. Jankovic D, Cheever AW, Kullberg MC, Wynn TA, Yap G, et al. (1998) CD4+ T Cell–mediated Granulomatous Pathology in Schistosomiasis Is Downregulated by a B Cell–dependent Mechanism Requiring Fc Receptor Signaling. J Exp Med 187: 619–629.
- 11. Chensue SW, Wellhausen SR, Boros DL (1981) Modulation of granulomatous hypersensitivity. II. Participation of Lyt1+and Lyt2+T lymphocytes in the suppression of granuloma formation and lymphokine production in Schistosoma mansoni-infected mice. J Immunol 127: 363–367.
- 12. Chensue SW, Warmington KS, Hershey SD, Terebuh PD, Othman M, et al. (1993) Evolving T cell responses in murine schistosomiasis. Th2 cells mediate secondary granulomatous hypersensitivity and are regulated by CD8+ T cells in vivo. J Immunol 151: 1391–1400.
- 13. Pearce EJ, Caspar P, Grzych JM, Lewis FA, Sher A (1991) Downregulation of Th1 cytokine production accompanies induction of Th2 responses by a parasitic helminth, Schistosoma mansoni.. J Exp Med 173: 159–166.
- 14. Chen PH, Zhou SL (1995) Cultivation in vitro of medical parasites. Beijing: Science Press 277–293 (in Chinese).
- 15. Ruppel A, Shi YE, Moloney NA (1990) Schistosoma mansoni and S.japonicum: comparison of levels of ultraviolet irradiation for vaccination of mice with cercariae. Parasitology 101: 23–26.
- 16. Moloney NA, Doenhoff MJ, Webbe G, Hinchcliffe P (1982) Studies on the host-parasite relationship of Schistosoma japonicum in normal and immunosuppressed mice. Parasite Immunol 4: 431–440.
- 17. Phillips SM, DiConza JJ, Gold JA, Reid WA (1977) Schistosomiasis in the congenitally athymic (nude) mouse. I. Thymic dependency of eosinophilia, granuloma formation, and host morbidity. J Immunol 118: 594–599.
- 18. Doenhoff M, Musallam R, Bain J, McGregor A (1978) Studies on the hostparasite relationship in Schistosoma mansoni- infected mice: the immunological dependence of parasite egg excretion. Immunology 35: 771–778.
- 19. Bosma GC, Custer RP, Bosma MJ (1983) A severe combined immunodeficiency mutant in the mouse. Nature 301: 527–530.
- 20. Custer RP, Bosma GC, Bosma MJ (1985) Severe combined immunodeficiency (SCID) in the mouse. Am J Path. 120: 464–477.
- 21. Doenhoff MJ, Musallam R, Bain J, McGregor A (1979) Studies on the host-parasite relationship in Schistosoma mansoni–infected mice: the immunological dependence of parasite egg excretion. Immunology 35: 771–778.
- 22. Mangan NE, Fallon RE, Smith P, Rooijen N, Mckenzie AN, et al. (2004) Helminth Infection Protects Mice from Anaphylaxis via IL-10-Producing B Cells. J Immunol 173: 6346–6356.
- 23. Mark S Wilson, Allen W Cheever, Sandra D White, et al. (2011) IL-10 Blocks the Development of Resistance to Re-Infection with Schistosoma mansoni. Plos Pathog 7: e1002171.
- 24. Harrison RA, Doenhoff MJ (1983) Retarded development of Schistosoma mansoni in immunosuppressed mice. Parasitology 86: 429–438.
- 25. Lamb EW, Crow ET, Lim KC, Liang YS, Lewis FA, et al. (2007) Conservation of CD4+ T cell-dependent developmental mechanisms in the blood fluke pathogens of humans. Int J Parasitol 37: 405–415.
- 26. Doenhoff MJ, Sabah AA, Fletcher C, Webbe G, Bain J (1987) Evidence for an immune-dependent action of praziquantel on Schistosoma mansoni in mice. Trans R Soc Trop Med Hyg 81: 947–951.
- 27. Cheever AW, Poindexter RW, Wynn TA (1999) Egg laying is delayed but worm fecundity is normal in SCID mice infected with Schistosoma japonicum and S. mansoni with or without recombinant tumor necrosis factor alpha treatment. Infect Immun 67: 2201–2208.
- 28. Mizoguchi A, Bhan AK (2006) A case for regulatory B cells. J Immunol 176: 705–710.
- 29. Harris N, Gause WC (2011) To B or not to B:B cells and the Th2-type immune response to helminths. Cell 32: 80–88.
- 30. Burdin N, Rousset F, Banchereau J (1997) B-cell-derived IL-10: production and function. Methods 11: 98–111.
- 31. Duddy ME, Alter A, Bar-Or A (2004) Distinct profiles of human B cell effector cytokines: a role in immune regulation? J Immunol 172: 3422–3427.
- 32. Amu S, Saunders SP, Kronenberg M, Mangan NE, Atzberger, et al (2010) Regulatory B cells prevent and reverse allergic airway inflammation via FoxP3-positive T regulatory cells in a murine model. J Allergy Clin Immunol 125: 1125–1127.
- 33. Smits HH, Hammad H, van Nimwegen M, Soullie T, Willart MA, et al. (2007) Protective effect of Schistosoma mansoni infection on allergic airway inflammation depends on the intensity and chronicity of infection. J Allergy Clin Immunol 120: 932–940.
- 34. Velupillai P, Harn DA (1994) Oligosaccharide-specific induction of interleukin 10 production by B220+ cells from schistosome-infected mice: a mechanism for regulation of CD4+ T-cell subsets. Proc Natl Acad Sci U S A 91: 18–22.
- 35. Velupillai P, Secor WE, Horauf AM, Harn DA (1997) B-1 cell (CD5+B220+) outgrowth in murine schistosomiasis is genetically restricted and is largely due to activation by polylactosamine sugars. J Immunol 158: 338–344.
- 36. Pearce EJ, Caspar P, Grzych JM, Lewis FA, Sher A (1991) Downregulation of Th1 cytokine production accompanies induction of Th2 responses by a parasitic helminth, Schistosoma mansoni.. J Exp Med 173: 159–166.
- 37. Flores Villanueva PO, Reiser H, Stadecker MJ (1994) Regulation of T helper cell responses in experimental murine schistosomiasis by IL-10: effect on expression of B7 and B7–2 costimulatory molecules by macrophages. J Immunol 153: 5190–5199.
- 38. Chensue SW, Warmington KS, Ruth J, Lincoln PM, Kunkel SL (1994) Cross-regulatory role of interferongamma (IFN-gamma), IL-4 and IL-10 in schistosome egg granuloma formation: in vivo regulation of Th activity and inflammation. Clin Exp Immunol 98: 395–400.
- 39. Flores Villanueva PO, Zheng XX, Storm TB, Stadecker MJ (1996) Recombinant IL-10 and IL-10/Fc treatment down-regulate egg antigen-specific delayed hypersensitivity reactions and egg granuloma formation in schistosomiasis. J Immunol 156: 3315–3120.
- 40. Abe T, Colley DG (1984) Modulation of Schistosoma mansoni egg–induced granuloma formation. III. Evidence for an anti-idiotypic, I-J–positive, I-J–restricted, soluble T suppressor factor. J Immunol 132: 2084–2088.
- 41. Montesano MA, Freeman GL, Secor WE, Colley DC (1997) Immunoregulatory idiotypes stimulate T helper 1 cytokine responses in experimental Schistosoma mansoni infections. J Immunol 158: 3800–3804.
- 42. Fairfax KC, Amiel E, King IL, Freitas TC, Mohrs M, et al. (2012) IL-10R blockade during chronic schistosomiasis mansoni results in the loss of B cells from the liver and the development of severe pulmonary disease. PLoS Pathog. 8(1): e1002490.
- 43. Falcão PL, Malaquias LC, Martins-Filho OA, Silveira AM, Passos VM, et al. (1998) Human Schistosomiasis mansoni: IL-10 modulates the in vitro granuloma formation. Parasite Immunol. 1998 20: 447–454.
- 44. Byram JE, von Lichtenberg F (1977) Altered schistosome granuloma formation in nude mice. Am J Trop Med Hyg 26: 944–956.
- 45. Byram JE, Doenhoff MJ, Musallam R, Brink LH, von Lichtenberg F (1979) Schistosoma mansoni infections in T-cell deprived mice, and the ameliorating effect of administering homologous chronic infection serum. II. Pathology. Am J Trop Med Hyg 28: 274–285.