Barabás É Éva, Falus András, Nagy Károly, Várkonyi Viktória, Temesvári Erzsébet, Horváth Attila
National Institute for Dermato-Venereology, Budapest, Hungary.
Pathol Oncol Res. 1997;3(1):68-73. doi: 10.1007/BF02893357.
In HIV infection, the decrease in the number and functional activity of lymphocytes is accompanied by atopia and an increased level of total IgE and some specific IgE antibodies. This could be explained by the Th2 dominance induced by HIV replication and so a Th1-Th2 switch could have prognostic value. We investigated the characteristic T-helper phenotype dominance and its relationship to cytokine expression and IgE immune response in the early stage of asymptomatic HIV infection. In the separated lymphocytes of i. asymptomatic HIV positive persons; ii. HIV negative homosexuals; iii. atopic patients; and iv. healthy controls, expression of mRNA for IFNg (Th1) and IL-10 (Th2) were determined by semiquantitative RT-PCR. The serum level of antibodies for HIV 1/2 and total/specific IgE were also determined. Transcription of mRNA of IFNg and IL-10 were more pronounced in HIV positive and atopic groups than in the healthy control, without lymphocyte phenotype dominance. In HIV negative persons, however, a significant Th2 dominance was detected. There was no significant difference in the IgE level between the 4 investigated groups. In the HIV positive cases, IL-10 expression and total serum IgE do not support a switch to Th2 dominance. In the atopic group, aside from the total IgE level, down regulation of IFNg was not observed. These results suggest a general activation of the immune system in the early stage of HIV infection.
在HIV感染中,淋巴细胞数量和功能活性的降低伴随着异位性以及总IgE和一些特异性IgE抗体水平的升高。这可以用HIV复制诱导的Th2优势来解释,因此Th1-Th2转换可能具有预后价值。我们研究了无症状HIV感染早期特征性辅助性T细胞表型优势及其与细胞因子表达和IgE免疫反应的关系。在分离的淋巴细胞中:i. 无症状HIV阳性者;ii. HIV阴性同性恋者;iii. 异位性患者;iv. 健康对照,通过半定量RT-PCR测定IFNg(Th1)和IL-10(Th2)的mRNA表达。还测定了HIV 1/2抗体以及总/特异性IgE的血清水平。IFNg和IL-10的mRNA转录在HIV阳性和异位性组中比在健康对照组中更明显,且无淋巴细胞表型优势。然而,在HIV阴性者中,检测到显著的Th2优势。4个研究组之间的IgE水平无显著差异。在HIV阳性病例中,IL-10表达和血清总IgE不支持向Th2优势的转换。在异位性组中,除了总IgE水平外,未观察到IFNg的下调。这些结果表明HIV感染早期免疫系统普遍激活。