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口服抗原后48小时内,功能性CD25 - 和CD25 + 黏膜调节性T细胞在肠道引流淋巴组织中被诱导产生。

Functional CD25- and CD25+ mucosal regulatory T cells are induced in gut-draining lymphoid tissue within 48 h after oral antigen application.

作者信息

Hauet-Broere Femke, Unger Wendy W J, Garssen Johan, Hoijer Maarten A, Kraal Georg, Samsom Janneke N

机构信息

Department of Molecular Cell Biology, VUMC, Amsterdam, The Netherlands.

出版信息

Eur J Immunol. 2003 Oct;33(10):2801-10. doi: 10.1002/eji.200324115.

DOI:10.1002/eji.200324115
PMID:14515264
Abstract

Oral antigen application induces tolerance, leading to suppression of a subsequent systemic challenge with this antigen. The suppression is mediated by mucosal regulatory T (Tr) cells that may differentiate from naive peripheral T cells in the gut-draining lymphoid tissue. However, little is known about the initial steps of this differentiation process. In this study we show that 48 h after oral OVA treatment, antigen-specific T cells in mesenteric lymph nodes (MLN) and Peyer's Patches (PP) were activated and had divided up to four times. The first division was already seen in PP after 24 h. Analysis of surface marker expression and cytokine secretion of the dividing antigen-specific T cells revealed that they sequentially obtained an activation- and memory-like phenotype. These cells secreted IL-2 in most stages of division but only transiently IFN-gamma whereas no IL-4 or IL-10 secretion was detected. Remarkably, 48 h after antigen application, isolated dividing cells were suppressive, as they transferred tolerance to naive mice. Even though CD25 was expressed heterogeneously, both CD25(+) and CD25(-) OVA-specific T cells from MLN could transfer tolerance. Together these findings show that differentiation of functional Tr cells occurs in the MLN and PP within 2 days after antigen ingestion and involves the generation of CD25(+) and CD25(-) antigen-specific T cells.

摘要

口服抗原可诱导耐受性,从而抑制随后用该抗原进行的全身性攻击。这种抑制作用由黏膜调节性T(Tr)细胞介导,这些细胞可能在肠道引流淋巴组织中由幼稚外周T细胞分化而来。然而,对于这一分化过程的初始步骤知之甚少。在本研究中,我们发现口服卵清蛋白(OVA)处理48小时后,肠系膜淋巴结(MLN)和派尔集合淋巴结(PP)中的抗原特异性T细胞被激活,并且已经分裂了多达四次。24小时后在PP中就已经观察到了第一次分裂。对正在分裂的抗原特异性T细胞的表面标志物表达和细胞因子分泌进行分析发现,它们依次获得了激活样和记忆样表型。这些细胞在大多数分裂阶段分泌白细胞介素-2(IL-2),但仅短暂分泌干扰素-γ(IFN-γ),未检测到IL-4或IL-10的分泌。值得注意的是,抗原应用48小时后,分离出的正在分裂的细胞具有抑制作用,因为它们将耐受性传递给了幼稚小鼠。尽管CD25的表达存在异质性,但来自MLN的CD25(+)和CD25(-) OVA特异性T细胞都可以传递耐受性。这些发现共同表明,功能性Tr细胞的分化在抗原摄入后2天内在MLN和PP中发生,并且涉及CD25(+)和CD25(-)抗原特异性T细胞的产生。

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