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细胞毒性T淋巴细胞相关抗原4(CTLA-4)的过表达通过一种依赖于CD28-B7的机制抑制T细胞反应。

CTLA-4 overexpression inhibits T cell responses through a CD28-B7-dependent mechanism.

作者信息

Engelhardt John J, Sullivan Timothy J, Allison James P

机构信息

Division of Immunology, Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

J Immunol. 2006 Jul 15;177(2):1052-61. doi: 10.4049/jimmunol.177.2.1052.

Abstract

CTLA-4 has been shown to be an important negative regulator of T cell activation. To better understand its inhibitory action, we constructed CTLA-4 transgenic mice that display constitutive cell surface expression of CTLA-4 on CD4 and CD8 T cells. In both in vivo and in vitro T cell responses, CTLA-4 overexpression inhibits T cell activation. This inhibition is dependent on B7 and CD28, suggesting that overexpressed CTLA-4 inhibits responses by competing with CD28 for B7 binding or by interfering with CD28 signaling. In addition, expression of the transgene decreases the number of CD25+Foxp3+ T cells in these mice, but does not affect their suppressive ability. Our data confirm the activity of CTLA-4 as a negative regulator of T cell activation and that its action may be by multiple mechanisms.

摘要

CTLA-4已被证明是T细胞活化的重要负调节因子。为了更好地理解其抑制作用,我们构建了CTLA-4转基因小鼠,这些小鼠在CD4和CD8 T细胞上组成性地表达CTLA-4细胞表面分子。在体内和体外T细胞反应中,CTLA-4的过表达均抑制T细胞活化。这种抑制作用依赖于B7和CD28,提示过表达的CTLA-4通过与CD28竞争结合B7或干扰CD28信号传导来抑制反应。此外,转基因的表达减少了这些小鼠中CD25+Foxp3+ T细胞的数量,但不影响其抑制能力。我们的数据证实了CTLA-4作为T细胞活化负调节因子的活性,并且其作用可能通过多种机制实现。

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