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否决抑制:T细胞耐受的外周途径。

Veto suppression: the peripheral way of T cell tolerization.

作者信息

Tscherning T, Claësson M H

机构信息

Laboratory of Experimental Immunology, Panum Institute, Copenhagen, Denmark.

出版信息

Exp Clin Immunogenet. 1993;10(4):179-88.

PMID:7907886
Abstract

Cells with veto activity induce a state of tolerance in T cell precursors with specificity for antigen determinants expressed on the surface of the veto-active cell. This state of tolerance is not strictly defined, but results in altered responses to specific antigen, such as decreased proliferation, decreased development of cytotoxicity and secretion of interleukins, down-regulated ability to reject grafts and expression of T cell and IL-2 receptors. Both clonal anergy and clonal deletion has been shown to operate in vetoed T cells. Veto-induced tolerance can be established in vitro and in vivo for both MHC class I and II as well as minor histocompatibility antigens. The most powerful veto activity is present in mature activated cytotoxic CD8+ T cells, but other cells including noncytotoxic cells are also capable of acting as veto cells. Thus it appears that veto activity per se is not confined to a certain cellular entity, but rather reflects a constitutively expressed immunoregulatory capability inherent to a broad array of activated T cell and non-T cell categories with their own distinct functions not related to their eventual veto activity.

摘要

具有否决活性的细胞会在对否决活性细胞表面所表达抗原决定簇具有特异性的T细胞前体中诱导出一种耐受状态。这种耐受状态并无严格定义,但会导致对特定抗原的反应发生改变,比如增殖减少、细胞毒性的发育及白细胞介素分泌减少、移植物排斥能力下调以及T细胞和白细胞介素-2受体的表达下调。克隆失能和克隆清除在被否决的T细胞中均有作用。否决诱导的耐受可在体外和体内针对MHC I类和II类以及次要组织相容性抗原建立。最强大的否决活性存在于成熟活化的细胞毒性CD8+ T细胞中,但包括非细胞毒性细胞在内的其他细胞也能够充当否决细胞。因此,似乎否决活性本身并不局限于某一特定细胞实体,而是反映了广泛的活化T细胞和非T细胞类别所固有的一种组成性表达的免疫调节能力,这些细胞具有与其最终否决活性无关的各自独特功能。

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