Suppr超能文献

对初始CD8(+)淋巴细胞的共刺激可诱导CD4表达并允许1型人类免疫缺陷病毒感染。

Costimulation of naive CD8(+) lymphocytes induces CD4 expression and allows human immunodeficiency virus type 1 infection.

作者信息

Kitchen S G, Korin Y D, Roth M D, Landay A, Zack J A

机构信息

Division of Hematology-Oncology, Department of Medicine, UCLA School of Medicine, Los Angeles, California 90095, USA.

出版信息

J Virol. 1998 Nov;72(11):9054-60. doi: 10.1128/JVI.72.11.9054-9060.1998.

Abstract

Human immunodeficiency virus type 1 (HIV-1) infection requires cell surface expression of CD4. Costimulation of CD8(+)/CD4(-) T lymphocytes by anti-CD3 and anti-CD28 antibodies or by allogeneic dendritic cells induced expression of CD4 and rendered these CD8 cells susceptible to HIV-1 infection. Naive CD45RA+ cells responded with greater expression of CD4 than did CD45RO+ cells. CD8(+) lymphocytes derived from fetal or newborn sources exhibited a greater tendency to express CD4, consistent with their naive states. This mechanism of infection suggests HIV-induced perturbation of the CD8 arm of the immune response and could explain the generally rapid disease progression seen in HIV-infected children.

摘要

1型人类免疫缺陷病毒(HIV-1)感染需要CD4在细胞表面表达。抗CD3和抗CD28抗体或同种异体树突状细胞对CD8(+)/CD4(-) T淋巴细胞的共刺激诱导了CD4的表达,并使这些CD8细胞易受HIV-1感染。初始CD45RA+细胞比CD45RO+细胞对CD4的表达反应更强。来自胎儿或新生儿来源的CD8(+)淋巴细胞表现出更大的CD4表达倾向,这与其初始状态一致。这种感染机制表明HIV诱导了免疫反应中CD8臂的扰动,并且可以解释在HIV感染儿童中普遍观察到的疾病快速进展情况。

相似文献

引用本文的文献

3
The Role of CD4CD8 T Cells in HIV Infection With Tuberculosis.CD4CD8 T 细胞在 HIV 合并结核感染中的作用。
Front Public Health. 2022 May 27;10:895179. doi: 10.3389/fpubh.2022.895179. eCollection 2022.
6
CD32 is enriched on CD4dimCD8bright T cells.CD32 在 CD4dimCD8bright T 细胞上富集。
PLoS One. 2020 Sep 22;15(9):e0239157. doi: 10.1371/journal.pone.0239157. eCollection 2020.

本文引用的文献

9
Co-stimulation in T cell responses.T细胞应答中的共刺激
Curr Opin Immunol. 1997 Jun;9(3):396-404. doi: 10.1016/s0952-7915(97)80087-8.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验