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作为HIV阳性患者临床病情发展预测指标的干扰素自发释放

Spontaneous release of interferon as a predictor of clinical evolution in HIV-positive subjects.

作者信息

Biglino A, Surbone A, Lipani F, Cappello N, Forno B, Pollono A M, Busso M, Pugliese A

机构信息

Istituto di Malattie Infettive, Università di Torino, Italy.

出版信息

Infection. 1991 Jan-Feb;19(1):7-12. doi: 10.1007/BF01643747.

Abstract

In order to establish a correlation with disease progression we prospectively evaluated ten clinical and immunologic parameters in 102 consecutive HIV-positive subjects. The eight immunologic variables were: in vitro spontaneous interferon release by peripheral blood monocytic cells, alpha- and gamma-interferon production induced by Newcastle Disease Virus and PHA, Multitest Mérieux score, PHA- and CON-A-induced lymphocyte transformation, absolute number of CD4+ cells and CD4/CD8 ratio, respectively. The two baseline clinical variables were risk factor and disease presentation. Generalized Wilcoxon analysis indicated a significant correlation of one clinical (disease presentation at entry) and three immunologic variables (spontaneous interferon release, CD4+ cell number, Multitest Mérieux) with disease progression. Baseline spontaneous release of alpha, acid-labile interferon showed the best correlation with disease progression, and appeared to be significantly associated with CD4+ cell loss. Spontaneous release of acid-labile alpha interferon by mononuclear cells in vitro could be highly predictive of disease evolution in HIV-Ab positive, AIDS-free subjects.

摘要

为了建立与疾病进展的相关性,我们前瞻性地评估了102例连续的HIV阳性受试者的10项临床和免疫学参数。八项免疫学变量分别为:外周血单核细胞体外自发干扰素释放、新城疫病毒和PHA诱导的α和γ干扰素产生、梅里埃多项试验评分、PHA和刀豆蛋白A诱导的淋巴细胞转化、CD4 + 细胞绝对数和CD4/CD8比值。两项基线临床变量为危险因素和疾病表现。广义威尔科克森分析表明,一项临床变量(入组时的疾病表现)和三项免疫学变量(自发干扰素释放、CD4 + 细胞数量、梅里埃多项试验)与疾病进展显著相关。基线时酸不稳定α干扰素的自发释放与疾病进展的相关性最佳,并且似乎与CD4 + 细胞丢失显著相关。体外单核细胞酸不稳定α干扰素的自发释放可高度预测HIV抗体阳性、无艾滋病受试者的疾病进展。

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