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由艾滋病患者的HIV-gp120和gp120特异性抗体诱导的人CD4转基因小鼠中T淋巴细胞的缺失。

Deletion of T lymphocytes in human CD4 transgenic mice induced by HIV-gp120 and gp120-specific antibodies from AIDS patients.

作者信息

Wang Z Q, Orlikowsky T, Dudhane A, Mittler R, Blum M, Lacy E, Riethmüller G, Hoffmann M K

机构信息

Department of Microbiology and Immunology, New York Medical College, Valhalla 10595.

出版信息

Eur J Immunol. 1994 Jul;24(7):1553-7. doi: 10.1002/eji.1830240715.

Abstract

CD4, a T cell receptor for major histocompatibility complex class II antigen, is a key regulator of immunological reactivities. When engaged together with the T cell antigen receptor, CD4 enhances immune reactions, whereas when ligated independently of the antigen receptor CD4 inhibits the activation of T cells or initiates their deletion. CD4 serves also as a receptor for the human immunodeficiency virus (HIV), which binds the receptor with high avidity through its envelope molecule, gp120. Studies in tissue culture have shown that its affinity to CD4 gives the virus opportunities to utilize CD4-mediated signaling and to manipulate immunocytes. We show here in human CD4 transgenic mice that appropriately cross-linked HIV envelope protein causes massive deletion of HIV-reactive T cells in vivo.

摘要

CD4是主要组织相容性复合体II类抗原的T细胞受体,是免疫反应的关键调节因子。当与T细胞抗原受体一起作用时,CD4增强免疫反应,而当独立于抗原受体进行连接时,CD4会抑制T细胞的活化或启动其清除。CD4还是人类免疫缺陷病毒(HIV)的受体,HIV通过其包膜分子gp120与该受体高亲和力结合。组织培养研究表明,其对CD4的亲和力使该病毒有机会利用CD4介导的信号传导并操纵免疫细胞。我们在此处的人类CD4转基因小鼠中表明,适当交联的HIV包膜蛋白会在体内导致大量HIV反应性T细胞的清除。

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