The role of mucosal T lymphocytes in regulating intestinal inflammation.

Springer seminars in immunopathology Pub Date : 2005-09-01 Epub Date: 2005-06-15 DOI:10.1007/s00281-005-0206-6
Holm H Uhlig, Fiona Powrie
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引用次数: 31

Abstract

Suppression of chronic intestinal inflammation by different subtypes of T cells has been described in recent years. In particular, naturally arising CD4(+)CD25(+) regulatory T cells and IL-10-producing regulatory T cell type 1 CD4(+) T lymphocytes have been implicated in the regulation of intestinal inflammation. Here we focus on the ability of CD4(+)CD25(+) regulatory T cells to suppress innate and T-cell responses and discuss implications for immunoregulation in human inflammatory bowel disease. Besides the modulation of lymphoproliferation, a role for CD4(+)CD25(+) T cells in down-modulation of innate immune responses is emerging and the immunoregulatory activities of regulatory T cells in vivo may be mediated via effects on dendritic cells. Considering the extraordinary regenerative potential of the intestinal mucosa, the ability to impede pathogenic T-cell responses by active regulation might be of particular therapeutic benefit for the treatment of chronic intestinal inflammatory diseases such as Crohn's disease and ulcerative colitis.

粘膜T淋巴细胞在调节肠道炎症中的作用。
近年来,不同亚型的T细胞对慢性肠道炎症的抑制已被描述。特别是,自然产生的CD4(+)CD25(+)调节性T细胞和产生il -10的调节性T细胞1型CD4(+) T淋巴细胞参与了肠道炎症的调节。在这里,我们关注CD4(+)CD25(+)调节性T细胞抑制先天和T细胞反应的能力,并讨论在人类炎症性肠病中免疫调节的意义。除了对淋巴细胞增殖的调节外,CD4(+)CD25(+) T细胞在下调先天免疫应答中的作用正在出现,体内调节性T细胞的免疫调节活性可能通过对树突状细胞的作用来介导。考虑到肠粘膜非凡的再生潜力,通过主动调节来阻止致病性t细胞反应的能力可能对治疗慢性肠道炎症性疾病(如克罗恩病和溃疡性结肠炎)具有特殊的治疗益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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