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HIV感染中CD45异构体表达异常。

Abnormalities of CD45 isoform expression in HIV infection.

作者信息

Mahalingam M, Pozniak A, McManus T J, Senaldi G, Vergani D, Peakman M

机构信息

Department of Immunology, King's College Hospital, London, United Kingdom.

出版信息

Clin Immunol Immunopathol. 1996 Nov;81(2):210-4. doi: 10.1006/clin.1996.0178.

Abstract

Using monoclonal antibodies against CD45, CD45RA, CD45RB, and CD45RO, the surface density of expression and proportions of different CD45 isoforms were analyzed on CD4+ and CD8+ T lymphocyte subsets in HIV+ patients and controls. Analysis of the relative specific fluorescence (RSF) of CD45 isoforms showed a significant reduction in expression of total CD45 and its isoforms, CD45RA, CD45RO, and CD45RB, on CD4+ and CD8+ lymphocyte subsets in HIV+ patients compared with controls. However, expression of phosphotyrosine in the cytoplasm of CD4+ and CD8+ lymphocytes did not differ significantly between HIV+ patients and controls. Percentages of "naive" CD45RA+RO- CD4+ and CD8+ lymphocytes were lower than control values in all HIV+ patients (P < 0.001). Compared with controls, HIV+ patients had similar percentages of "memory" CD45RA-RO+ CD4+ lymphocytes but significantly higher percentages of memory CD8+ lymphocytes (P < 0.001). Percentages of memory CD8+ lymphocytes were lowest in patients with AIDS (P < 0.001). The consistent reduction in surface expression of all CD45 isoforms observed in our study may be of relevance to the impaired T cell activation characteristic of HIV infection. Also, our results argue against the selective depletion of memory CD4+ lymphocytes in HIV-induced disease.

摘要

利用抗CD45、CD45RA、CD45RB和CD45RO的单克隆抗体,分析了HIV阳性患者和对照者CD4+和CD8+ T淋巴细胞亚群上不同CD45异构体的表面表达密度和比例。CD45异构体相对特异性荧光(RSF)分析显示,与对照相比,HIV阳性患者CD4+和CD8+淋巴细胞亚群上总CD45及其异构体CD45RA、CD45RO和CD45RB的表达显著降低。然而,HIV阳性患者和对照者CD4+和CD8+淋巴细胞细胞质中磷酸酪氨酸的表达没有显著差异。所有HIV阳性患者中,“初始”CD45RA+RO-CD4+和CD8+淋巴细胞的百分比均低于对照值(P<0.001)。与对照相比,HIV阳性患者“记忆”CD45RA-RO+CD4+淋巴细胞的百分比相似,但记忆CD8+淋巴细胞的百分比显著更高(P<0.001)。艾滋病患者中记忆CD8+淋巴细胞的百分比最低(P<0.001)。我们研究中观察到的所有CD45异构体表面表达的持续降低可能与HIV感染特有的T细胞活化受损有关。此外,我们的结果反对HIV诱导疾病中记忆CD4+淋巴细胞的选择性耗竭。

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