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表达 CD8 和 T 细胞受体 γδ 的小肠上皮内淋巴细胞参与鼠伤寒沙门氏菌感染期间的细菌清除。

Small intestinal intraepithelial lymphocytes expressing CD8 and T cell receptor γδ are involved in bacterial clearance during Salmonella enterica serovar Typhimurium infection.

机构信息

Institute of Immunopharmacology & Immunotherapy, School of Pharmaceutical Sciences, Shandong University, Jinan, China.

出版信息

Infect Immun. 2012 Feb;80(2):565-74. doi: 10.1128/IAI.05078-11. Epub 2011 Dec 5.

Abstract

The intestinal immune system is crucial for the maintenance of mucosal homeostasis and has evolved under the dual pressure of protecting the host from pathogenic infection and coexisting with the dense and diverse commensal organisms in the lumen. Intestinal intraepithelial lymphocytes (iIELs) are the first element of the host T cell compartment available to respond to oral infection by pathogens. This study demonstrated that oral infection by Salmonella enterica serovar Typhimurium promoted the expansion of iIELs, particularly CD8(+) TCRγδ(+) IELs, enhanced expression of NKG2D on iIELs, increased expression of MULT1, and decreased expression of Qa-1 by intestinal epithelial cells (IECs), leading to activation of, particularly, CD8(+) TCRγδ(+) iIELs and cytolytic activity against S. Typhimurium-infected IECs. Blockade of NKG2D recognition or depletion of TCRγδ(+) cells using a depleting monoclonal antibody significantly attenuated the clearance of S. Typhimurium in the intestine and other tissues. This study suggests that iIELs, particularly CD8(+) TCRγδ(+) iIELs, play important roles in the detection of pathogenic bacteria and eradication of infected epithelial cells and, thus, provide protection against invading pathogens. These data further our understanding of the mechanisms by which the immune system of the intestinal mucosa discriminates between pathogenic and commensal organisms.

摘要

肠道免疫系统对于维持黏膜稳态至关重要,它在保护宿主免受病原感染和与腔道中密集多样的共生生物共存的双重压力下进化而来。肠道上皮内淋巴细胞 (iIEL) 是宿主 T 细胞区室中对病原体经口感染作出反应的第一个元素。本研究表明,鼠伤寒沙门氏菌经口感染促进了 iIEL 的扩增,特别是 CD8(+) TCRγδ(+) IEL 的扩增,增强了 iIEL 上 NKG2D 的表达,增加了 MULT1 的表达,降低了肠道上皮细胞 (IEC) 上 Qa-1 的表达,导致特别是 CD8(+) TCRγδ(+) iIEL 的激活和对受感染的 IEC 进行细胞溶解。使用耗竭单克隆抗体阻断 NKG2D 识别或耗竭 TCRγδ(+) 细胞,可显著减弱肠道和其他组织中鼠伤寒沙门氏菌的清除。本研究表明,iIEL,特别是 CD8(+) TCRγδ(+) iIEL,在检测致病性细菌和清除受感染的上皮细胞方面发挥重要作用,从而为抵御入侵病原体提供保护。这些数据进一步了解了肠道黏膜免疫系统区分病原生物和共生生物的机制。

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