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通过预先感染非致病性病毒预防免疫缺陷病毒诱导的CD4 + T细胞耗竭。

Prevention of immunodeficiency virus induced CD4+ T-cell depletion by prior infection with a non-pathogenic virus.

作者信息

Terwee Julie A, Carlson Jennifer K, Sprague Wendy S, Sondgeroth Kerry S, Shropshire Sarah B, Troyer Jennifer L, VandeWoude Sue

机构信息

Department of Microbiology, Immunology and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado, USA.

出版信息

Virology. 2008 Jul 20;377(1):63-70. doi: 10.1016/j.virol.2008.03.037. Epub 2008 May 22.

Abstract

Immune dysregulation initiated by a profound loss of CD4+ T-cells is fundamental to HIV-induced pathogenesis. Infection of domestic cats with a non-pathogenic lentivirus prevalent in the puma (puma lentivirus, PLV or FIV(pco)) prevented peripheral blood CD4+ T-cell depletion caused by subsequent virulent FIV infection. Maintenance of this critical population was not associated with a significant decrease in FIV viremia, lending support to the hypothesis that direct viral cytopathic effect is not the primary cause of immunodeficiency. Although this approach was analogous to immunization with a modified live vaccine, correlates of immunity such as a serum-neutralizing antibody or virus-specific T-cell proliferative response were not found in protected animals. Differences in cytokine transcription profile, most notably in interferon gamma, were observed between the protected and unprotected groups. These data provide support for the importance of non-adaptive enhancement of the immune response in the prevention of CD4+ T-cell loss.

摘要

由CD4 + T细胞大量丧失引发的免疫失调是HIV诱导发病机制的根本。用美洲狮中普遍存在的一种非致病性慢病毒(美洲狮慢病毒,PLV或FIV(pco))感染家猫,可预防随后强毒FIV感染引起的外周血CD4 + T细胞耗竭。维持这一关键细胞群与FIV病毒血症的显著降低无关,这支持了直接病毒细胞病变效应不是免疫缺陷主要原因的假说。尽管这种方法类似于用减毒活疫苗进行免疫,但在受保护的动物中未发现免疫相关指标,如血清中和抗体或病毒特异性T细胞增殖反应。在受保护组和未受保护组之间观察到细胞因子转录谱的差异,最显著的是干扰素γ。这些数据支持了免疫反应的非适应性增强在预防CD4 + T细胞丧失中的重要性。

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