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西尼罗河黄病毒对免疫识别分子的调控

Regulation of immune recognition molecules by flavivirus, West Nile.

作者信息

Kesson Alison M, Cheng Ying, King Nicholas J C

机构信息

Department of Virology and Microbiology, The Children's Hospital at Westmead, NSW, Australia.

出版信息

Viral Immunol. 2002;15(2):273-83. doi: 10.1089/08828240260066224.

Abstract

We have shown the flaviviruses can up-regulate the cell surface expression of the immune recognition molecules, major histocompatability complex class-I and class-II (MHC-I, MHC-II), ICAM-1, VCAM, and E-selectin, in an interferon-independent and tumor necrosis factor-independent manner. This up-regulation is associated with an increased transcription of the relevant genes and is due to activation of the transcription factor, nuclear factor-kappa B. The level of up-regulation is determined in part by the cell cycle position of the cell when infected with the flavivirus, as quiescent cells show a greater increase in the level of expression of the immune recognition molecules, MHC-I and ICAM-1, than cells in other phases of the cell cycle. The resultant increased cell surface expression is functional with the increased expression resulting in increased recognition by flavivirus-specific and allo-specific cytotoxic T cells.

摘要

我们已经证明,黄病毒能够以不依赖干扰素和不依赖肿瘤坏死因子的方式上调免疫识别分子的细胞表面表达,这些分子包括主要组织相容性复合体I类和II类(MHC-I、MHC-II)、细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子(VCAM)和E-选择素。这种上调与相关基因转录增加有关,并且是由于转录因子核因子-κB的激活所致。上调水平部分取决于感染黄病毒时细胞的细胞周期位置,因为静止细胞相比处于细胞周期其他阶段的细胞,在免疫识别分子MHC-I和ICAM-1的表达水平上有更大的增加。由此产生的细胞表面表达增加具有功能性,这种增加的表达导致黄病毒特异性和同种特异性细胞毒性T细胞的识别增加。

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