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在对感染的免疫反应早期阶段非特异性T细胞的选择性耗竭。

Selective depletion of nonspecific T cells during the early stage of immune responses to infection.

作者信息

Jiang Jiu, Lau Lisa L, Shen Hao

机构信息

Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6076, USA.

出版信息

J Immunol. 2003 Oct 15;171(8):4352-8. doi: 10.4049/jimmunol.171.8.4352.

Abstract

Transient T cell depletion occurs before the development of an effective immune response to infection. In this study we show that most T cells, regardless of specificity, are induced to express early activation markers soon after infection with Listeria monocytogenes or lymphocytic choriomeningitis virus. Ag-specific T cells are further activated to display late activation markers and undergo extensive proliferation. As Ag-specific T cells begin to expand, nonspecific T cells are depleted en masse and exhibit no sign of further activation or proliferation before their depletion. This selective depletion of nonspecific T cells is due to in situ death via apoptosis, as visualized by confocal microscopy. Thus, early activation and subsequent depletion of nonspecific T cells are integral parts of the immune response to proinflammatory infections. These results have important implications for our understanding of early events in the development of a robust T cell response.

摘要

在对感染产生有效的免疫反应之前,会发生短暂的T细胞耗竭。在本研究中,我们发现,大多数T细胞,无论其特异性如何,在感染单核细胞增生李斯特菌或淋巴细胞性脉络丛脑膜炎病毒后不久,就会被诱导表达早期激活标志物。抗原特异性T细胞会进一步被激活,以显示晚期激活标志物并进行广泛增殖。随着抗原特异性T细胞开始扩增,非特异性T细胞会大量耗竭,并且在耗竭之前没有进一步激活或增殖的迹象。非特异性T细胞的这种选择性耗竭是由于通过共聚焦显微镜观察到的原位凋亡死亡。因此,非特异性T细胞的早期激活和随后的耗竭是对促炎性感染免疫反应的组成部分。这些结果对于我们理解强大的T细胞反应发展中的早期事件具有重要意义。

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