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日本血吸虫病小鼠卵中的热休克蛋白60特异性诱导调节性T细胞并减轻肝脏免疫病理损伤。

Heat Shock Protein 60 in Eggs Specifically Induces Tregs and Reduces Liver Immunopathology in Mice with Schistosomiasis Japonica.

作者信息

Zhou Sha, Jin Xin, Chen Xiaojun, Zhu Jifeng, Xu Zhipeng, Wang Xuefeng, Liu Feng, Hu Wei, Zhou Liang, Su Chuan

机构信息

Department of Pathogen Biology and Immunology, Jiangsu Key Laboratory of Pathogen Biology, Nanjing Medical University, Nanjing, Jiangsu, China.

Department of Microbiology and Microbial Engineering, School of Life Science, Fudan University, Shanghai, China.

出版信息

PLoS One. 2015 Sep 29;10(9):e0139133. doi: 10.1371/journal.pone.0139133. eCollection 2015.

Abstract

BACKGROUND

Parasitic helminths need to suppress the host immune system to establish chronic infections. Paradoxically, immunosuppression induced by the worm also benefits the host by limiting excessive inflammation and tissue damage, which remains the major cause leading to serious morbidity and mortality. Regulatory T cells (Tregs) are key immune regulators of this mutualism. The successive rise in Tregs during schistosome infection plays a critical role in immunoregulation. We and others previously showed that Schistosoma japonicum (S. japonicum) egg antigens (SEA) induce Tregs both in vitro and in vivo. In addition, we identified that SjHSP60 derived from SEA significantly induces Tregs in vivo and in vitro. However, the contribution of SjHSP60 in SEA to Treg induction and the related mechanisms of the Treg induction have not yet been identified.

METHODOLOGY/PRINCIPAL FINDINGS: In this study, we showed that S. japonicum stress protein HSP60 (SjHSP60) was constitutively and extensively expressed in eggs of S. japonicum. SjHSP60 specially induced Tregs in vivo and in vitro without inducing other CD4+ T sub-populations including Th1, Th2 and Th17 cells. Furthermore, we showed that the SjHSP60-depleted SEA almost lost the ability in vitro and displayed a significant impaired ability to induce Tregs in vivo. Finally, our study illustrated that the mechanisms of SjHSP60-mediated induction of Tregs are through both conversion of CD4+CD25- T cells into CD4+CD25+Foxp3+ Tregs and expansion of preexisting CD4+CD25+Foxp3+ Tregs in a TLR4-dependent manner.

CONCLUSIONS/SIGNIFICANCE: Collectively, our findings identify SjHSP60 as a major parasitic contributor of Treg induction in S. japonicum egg antigens, which not only contributes to the better understanding of the mechanism of immunoregulation during helminth infection, but also suggests its potential as a therapeutic target for control of immunopathology, allergic and autoimmune diseases.

摘要

背景

寄生性蠕虫需要抑制宿主免疫系统以建立慢性感染。矛盾的是,蠕虫诱导的免疫抑制通过限制过度炎症和组织损伤也对宿主有益,而过度炎症和组织损伤仍然是导致严重发病和死亡的主要原因。调节性T细胞(Tregs)是这种共生关系的关键免疫调节因子。血吸虫感染期间Tregs的持续增加在免疫调节中起关键作用。我们和其他人之前表明,日本血吸虫(S. japonicum)卵抗原(SEA)在体外和体内均可诱导Tregs。此外,我们确定源自SEA的SjHSP60在体内和体外均能显著诱导Tregs。然而,SEA中的SjHSP60对Treg诱导的贡献以及Treg诱导的相关机制尚未明确。

方法/主要发现:在本研究中,我们表明日本血吸虫应激蛋白HSP60(SjHSP60)在日本血吸虫卵中组成性且广泛表达。SjHSP60在体内和体外特异性诱导Tregs,而不诱导包括Th1、Th2和Th17细胞在内的其他CD4 + T亚群。此外,我们表明去除SjHSP60的SEA在体外几乎丧失了诱导能力,并且在体内诱导Tregs的能力显著受损。最后,我们的研究表明SjHSP60介导的Treg诱导机制是通过将CD4 + CD25 - T细胞转化为CD4 + CD25 + Foxp3 + Tregs以及以TLR4依赖性方式扩增预先存在的CD4 + CD25 + Foxp3 + Tregs。

结论/意义:总体而言,我们的研究结果确定SjHSP60是日本血吸虫卵抗原中Treg诱导的主要寄生虫贡献因子,这不仅有助于更好地理解蠕虫感染期间的免疫调节机制,还表明其作为控制免疫病理、过敏性和自身免疫性疾病的治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7393/4587937/fe50651c40c2/pone.0139133.g001.jpg

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