hiv感染者的单核细胞毒性抗体。tnf - α处理U937细胞增加补体依赖性细胞毒性。

Acta microbiologica Hungarica Pub Date : 1993-01-01
B Szabó, C Locardi, E Lo Presti, A Benedetto, F Belardelli
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引用次数: 0

摘要

对40名静脉注射吸毒成瘾者的血清进行了细胞毒抗体检测,以对抗未感染和感染hiv的单核细胞U937。31个血清阳性样本中有12个在补体存在的情况下对hiv感染、未经处理的靶细胞具有细胞毒性。tnf - α处理hiv感染的U937细胞可提高血清细胞毒性作用的可检测性(21/31)。重组HIV gp120预处理可降低血清补体依赖性细胞毒活性。在大多数情况下,这种减少证明是剂量依赖性的。免疫荧光研究表明,细胞毒性血清与主要定位于hiv感染的tnf - α处理的U937细胞细胞膜上的抗原相互作用。本文讨论了hiv感染者单核细胞毒性抗体的特异性、可能的作用和来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Monocytotoxic antibodies in HIV-infected persons. TNF-alpha treatment of U937 cells increases the complement dependent cytotoxicity.

Sera of 40 intravenous drug addicts were tested for the presence of cytotoxic antibodies against uninfected and HIV-infected monocytic U937 cells. Twelve out of 31 seropositive samples proved to be cytotoxic for HIV-infected, untreated target cells in the presence of complement. The TNF-alpha treatment of HIV-infected U937 cells increased the detectability of cytotoxic effect of sera (21/31). The complement dependent cytotoxic activity of sera was reduced by pretreatment with recombinant HIV gp120. This reduction proved to be dose-dependent in the majority of cases. Immunofluorescence studies indicated that the cytotoxic sera interacted with antigens mostly localized on the cell membrane of HIV-infected TNF-alpha treated U937 cells. The specificity, the possible role and origin of monocytotoxic antibodies in HIV-infected persons is discussed.

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