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由于CCR5的诱导,恒河猴外周血CD4和CD8双阳性T细胞通过体外刺激变得易受猴免疫缺陷病毒感染。

Peripheral blood CD4 and CD8 double-positive T cells of rhesus macaques become vulnerable to Simian Immunodeficiency Virus by in vitro stimulation due to the induction of CCR5.

作者信息

Matsumoto Yusuke, Miura Tomoyuki, Akari Hirofumi, Goto Yoshitaka, Haga Takeshi

机构信息

Department of Veterinary Microbiology, University of Miyazaki, Miyazaki, Japan.

出版信息

J Vet Med Sci. 2010 Aug;72(8):1057-61. doi: 10.1292/jvms.09-0588. Epub 2010 Mar 12.

Abstract

In vivo Simian Immunodeficiency Virus (SIV) challenge of macaques demonstrated the earlier disappearance of CD4 and CD8 double-positive (DP) T cells than CD4 single-positive T cells, although its mechanism remains unclear. Here we found that peripheral DP T cells were readily induced to express CCR5, a secondary receptor for SIV, by in vitro stimulation with either concanavalin A or anti-CD3/CD28 monoclonal antibodies. Activated DP T cells were more vulnerable to SIV infection, indicating that the ability of DP T cells to readily express CCR5 after activation may hasten DP T cell death by SIV infection in vivo.

摘要

猕猴的体内猿猴免疫缺陷病毒(SIV)攻击试验表明,CD4和CD8双阳性(DP)T细胞比CD4单阳性T细胞更早消失,尽管其机制尚不清楚。在这里,我们发现,通过伴刀豆球蛋白A或抗CD3/CD28单克隆抗体进行体外刺激,外周血DP T细胞很容易被诱导表达SIV的辅助受体CCR5。活化的DP T细胞更容易受到SIV感染,这表明DP T细胞在活化后易于表达CCR5的能力可能会加速体内SIV感染导致的DP T细胞死亡。

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