总T细胞计数下降与艾滋病发病有关,与CD4+淋巴细胞计数无关:对艾滋病发病机制的影响

Joseph B. Margolick , Albert D. Donnenberg , Clara Chu , Maurice R.G. O'Gorman , Janis V. Giorgi , Alvaro Muñoz
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引用次数: 25

摘要

我们之前报道了盲T细胞稳态,其中T细胞总数保持不变,但T细胞的CD4+和CD8+亚群组成可能发生变化,在艾滋病发病前约1.5至2.5年失效。本研究的前提假设是,如果T细胞稳态的失败(即总T细胞计数的下降)在艾滋病的发病机制中很重要,那么在控制CD4+淋巴细胞计数后,它应该是艾滋病的一个重要预测因子。研究人员评估了1556名具有足够序列T细胞亚群测量值的男同性恋者的数据,这些数据代表了在超过10年的时间里有已知临床结果的11988名男性患者。利用结合CD4+淋巴细胞计数和hiv相关症状(发热、鹅口疮)的回归模型,我们确定,对于CD4+淋巴细胞计数为500细胞/μl的受试者,外周血T细胞每年下降超过300个/μl是艾滋病发病的独立预测因子。这些结果支持了T细胞稳态失败在艾滋病发病机制中的重要作用。
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Decline in Total T Cell Count Is Associated with Onset of AIDS, Independent of CD4+Lymphocyte Count: Implications for AIDS Pathogenesis

We previously reported that blind T cell homeostasis, in which the total T cell count is maintained but the CD4+and CD8+subset composition of the T cells can vary, fails approximately 1.5 to 2.5 years before the onset of AIDS. The present study was premised on the hypothesis that if failure of T cell homeostasis (i.e., a decline in total T cell counts) is important in the pathogenesis of AIDS, it should be a significant predictor of AIDS after controlling for the CD4+lymphocyte count. Data from 1556 homosexual men with sufficient sequential T cell subset measurements were evaluated, representing 11,988 person-visits in men with known clinical outcomes over a period of more than 10 years. Using regression models that incorporated CD4+lymphocyte count and HIV-related symptoms (fever, thrush), it was determined that a yearly decline of more than 300 T cells/μl of peripheral blood was an independent predictor of the onset of AIDS for subjects with CD4+lymphocyte counts of <500 cells/μl. The results support an important role for failure of T cell homeostasis in the pathogenesis of AIDS.

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