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血吸虫卵肉芽肿巨噬细胞诱导T辅助细胞对抗原无反应性。这是血吸虫病免疫调节的基础吗?

Induction of T helper cell unresponsiveness to antigen by macrophages from schistosomal egg granulomas. A basis for immunomodulation in schistosomiasis?

作者信息

Stadecker M J, Kamisato J K, Chikunguwo S M

机构信息

Department of Pathology, Tufts University School of Medicine, Boston, MA 02111.

出版信息

J Immunol. 1990 Oct 15;145(8):2697-700.

PMID:2145363
Abstract

The present studies were undertaken in an effort to understand the role of mononuclear phagocytes in the regulation of the T cell-mediated granulomatous inflammatory response in experimental murine schistosomiasis mansoni. We report that macrophages from schistosomal egg granulomas did not efficiently stimulate, but rather induced marked proliferative unresponsiveness to Ag in an IL-2-producing, I-Ek-restricted, CD4+ Th cell clone specific for pigeon cytochrome c. The unresponsive state of the T cells was achieved after incubation with granuloma macrophages in the presence of the specific Ag fragment 81-104, but not with either of them independently, and was, similarly, restricted by the I-Ek molecule. Equivalent amounts of peritoneal macrophages from schistosome-infected, but not from normal mice, were also effective in inducing T cell unresponsiveness. We postulate that granuloma macrophages, and potentially other accessory cells in schistosome-infected individuals, are similarly capable of inducing anergy in egg Ag-specific Th cells, and that the resulting inhibited T cell reactivity, which translates into failure of lymphokine secretion and of clonal expansion, represents a major basis of the immunologic down-regulation (immunomodulation) of granulomatous hypersensitivity, characteristically seen in this disease.

摘要

本研究旨在了解单核吞噬细胞在实验性小鼠曼氏血吸虫病中T细胞介导的肉芽肿性炎症反应调节中的作用。我们报告,来自血吸虫卵肉芽肿的巨噬细胞不能有效地刺激,反而在针对鸽细胞色素c的产生白细胞介素-2、受I-Ek限制的CD4 + Th细胞克隆中诱导对Ag的明显增殖无反应性。T细胞的无反应状态是在特异性Ag片段81 - 104存在下与肉芽肿巨噬细胞孵育后实现的,而不是单独与它们中的任何一个孵育,并且同样受I-Ek分子限制。来自感染血吸虫的小鼠而非正常小鼠的等量腹腔巨噬细胞也能有效诱导T细胞无反应性。我们推测,肉芽肿巨噬细胞以及血吸虫感染个体中潜在的其他辅助细胞同样能够诱导卵Ag特异性Th细胞无反应,并且由此产生的T细胞反应性抑制,表现为淋巴因子分泌和克隆扩增失败,是这种疾病中典型的肉芽肿性超敏反应免疫下调(免疫调节)的主要基础。

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