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Immunomodulatory effects of Eimeria maxima surface antigen (EmSAG) as an IFN-γ inhibitory molecule on peripheral blood mononuclear cells (PBMCs) and T cell subsets in chickens

文献类型： 外文期刊

作者： Pu, Xianglin 1 ; Zhang, Yiyuan 1 ; Huang, Xinmei 2 ; Lu, Mingmin 1 ; Xu, Lixin 1 ; Yan, Ruofeng 1 ; Li, Xiangrui 1 ; Song, Xiaokai 1 ;

作者机构： 1.Nanjing Agr Univ, Coll Vet Med, Minist Educ MOE, Joint Int Res Lab Anim Hlth & Food Safety, Nanjing 210095, Peoples R China

2.Jiangsu Acad Agr Sci, Inst Vet Med, Nanjing 210014, Peoples R China

关键词： IFN-gamma inhibitory molecule; EmSAG; T cell subsets; immune evasion; immunomodulation

期刊名称：VETERINARY RESEARCH （ 影响因子：3.5； 五年影响因子：4.0 ）

ISSN： 0928-4249

年卷期： 2025 年 56 卷 1 期

页码：

收录情况： SCI

摘要： Eimeria maxima (E. maxima) infection inhibits the expression of IFN-gamma, a cytokine that is essential for the Th1 immune response and plays a key role in combating this parasite. In our preliminary investigations, we identified the E. maxima surface antigen (EmSAG) as an inhibitory molecule of IFN-gamma. EmSAG was screened and characterised from an E. maxima sporozoite cDNA expression library. The present study aimed to evaluate the immunomodulatory effects of EmSAG on chicken peripheral blood mononuclear cells (PBMCs) and various T cell subsets. We analysed cell proliferation, nitric oxide (NO) release, and cytokine transcription. The results revealed that EmSAG boosts PBMC proliferation and promotes differentiation of CD4+/CD8+ T cells. Additionally, stimulation with EmSAG significantly inhibited NO release and IFN-gamma transcription while enhancing the transcription of IL-4, IL-10, and TGF-beta 1 in chicken PBMCs. The sorting purity of T cell subsets was as follows: CD8+ (96.90%), CD4+ (86.25%), CD4+CD25- (89.14%), and CD4+CD25+ regulatory T cells (Tregs; 92.16%). These purified subsets were co-incubated with EmSAG to analyse the transcription of hallmark cytokines associated with Th1, Th2, and Treg responses. EmSAG significantly inhibited the transcription of IFN-gamma and IL-2 in both CD4+ and CD8+ T cells, while promoting the expression of IL-10, TGF-beta 1, and CTLA-4 in Tregs. Moreover, depletion of CD25+ cells reversed the EmSAG-induced suppression of IL-2 transcription and reduced its stimulating effects on IL-4 and IL-10 transcription in CD4+CD25- T cells. These findings highlight the role of EmSAG as an inhibitor of IFN-gamma, facilitating immune evasion by attenuating the Th1 immune response and modulating Treg cell function. This study provides critical insights into the immune evasion mechanisms utilised by chicken coccidia.

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