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在人类免疫缺陷病毒1型感染期间,在外周血淋巴细胞上定量检测到的CD4掩盖现象是疾病进展的一个潜在标志物。

CD4 masking during human immunodeficiency virus type 1 infection, quantified on peripheral blood lymphocytes, is a potential marker of disease progression.

作者信息

Carrière D, Vendrell J, Berthier A, Atoui N, Salhi S L, Reynes J, Gros P, Fontaine C, Jansen A, Huguet M, Ait-Cheik L, Pau B

机构信息

Sanofi Recherche (Laboratoire d'Immunologie), Montpellier, France.

出版信息

J Infect Dis. 1996 Mar;173(3):565-73. doi: 10.1093/infdis/173.3.565.

Abstract

In human immunodeficiency virus type 1 (HIV-1)-infected adults, the proportion of gp120-free CD4 molecules on the surface of T lymphocytes was measured by double-epitope EIA and expressed as a CD epitope concentration ratio. In 51% of these patients (n=81), CD4 T cells showed a significant decrease (up to 100%) in the accessibility of the CD4 epitope in the D1 domain remained accessible. Of interest, a significant increase in the CD4 gp120 binding site concentration, without a change in T cell counts, was observed within 10 days after initiation of zidovudine treatment. Furthermore, CD4 masking by gp120 was associated with a poor clinical patient status. The assessment of the CD4 epitope concentration ratio is proposed as a surrogate marker of disease progression in HIV-1-infected patients.

摘要

在人类免疫缺陷病毒1型(HIV-1)感染的成年人中,通过双表位酶联免疫吸附测定法(EIA)测量T淋巴细胞表面无gp120的CD4分子比例,并将其表示为CD表位浓度比。在这些患者的51%(n = 81)中,CD4 T细胞显示D1结构域中CD4表位的可及性显著降低(高达100%),而该结构域仍可及。有趣的是,在齐多夫定治疗开始后的10天内,观察到CD4 gp120结合位点浓度显著增加,而T细胞计数没有变化。此外,gp120对CD4的掩盖与患者的不良临床状态相关。建议将CD4表位浓度比的评估作为HIV-1感染患者疾病进展的替代标志物。

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