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gp120-induced programmed cell death in recently activated T cells without subsequent ligation of the T cell receptor.

作者信息

Foster S, Beverley P, Aspinall R

机构信息

Department of Medicine, St. Mary's Hospital Medical School, London, GB.

出版信息

Eur J Immunol. 1995 Jun;25(6):1778-82. doi: 10.1002/eji.1830250644.

DOI:10.1002/eji.1830250644
PMID:7615007
Abstract

In most individuals, HIV infection is characterized by a progressive decline in the number of peripheral blood CD4+ T lymphocytes, and while the number of CD4+ cells is within the normal range, defects in immune function are detectable. To date neither the decline in function nor the decline in cell number have been satisfactorily explained. Here we describe a mechanism which may contribute to the immunodeficiency and decline in CD4+ cell numbers in HIV-infected individuals. We show that recently activated T cells are susceptible to apoptosis when exposed to HIV gp120 in the presence of anti-gp120 antibody.

摘要

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引用本文的文献

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Microbiol Mol Biol Rev. 2000 Dec;64(4):725-45. doi: 10.1128/MMBR.64.4.725-745.2000.
3
Highly active anti-retroviral therapy (HAART) is associated with a lower level of CD4+ T cell apoptosis in HIV-infected patients.
高效抗逆转录病毒疗法(HAART)与HIV感染患者较低水平的CD4 + T细胞凋亡有关。
Clin Exp Immunol. 1999 Dec;118(3):412-6. doi: 10.1046/j.1365-2249.1999.01076.x.
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T helper cell activation and human retroviral pathogenesis.辅助性T细胞激活与人类逆转录病毒发病机制。
Microbiol Rev. 1996 Dec;60(4):722-42. doi: 10.1128/mr.60.4.722-742.1996.
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