Chougnet C, Wynn T A, Clerici M, Landay A L, Kessler H A, Rusnak J, Melcher G P, Sher A, Shearer G M
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-1360, USA.
J Infect Dis. 1996 Jul;174(1):46-53. doi: 10.1093/infdis/174.1.46.
Human immunodeficiency virus (HIV) disease is associated with loss of type 1 responses, including interleukin (IL)-12 production. The dramatic drop in p70 production seen at early stages of disease was found not to be associated with a similarly decreased p40 mRNA expression. p35 mRNA expression was more extensively reduced than p40 mRNA expression at these early stages. Monocytes infected in vitro with HIV displayed decreased p35 expression and p70 production, suggesting that such decreased IL-12 expression may contribute to reduced IL-12 production in HIV-positive patients' cells. In addition, treatment of cells with IL-10 increased IL-10 mRNA expression and decreased p40 expression in both HIV-positive and -negative cells, while neutralization of IL-10 increased p40 mRNA levels. These observations, together with the observed hyperproduction of IL-10 in HIV-positive patients, may explain the dysregulation of IL-12 production seen in HIV disease.
人类免疫缺陷病毒(HIV)疾病与1型免疫反应的丧失有关,包括白细胞介素(IL)-12的产生。在疾病早期观察到的p70产生的显著下降,被发现与p40 mRNA表达的类似下降无关。在这些早期阶段,p35 mRNA表达比p40 mRNA表达减少得更广泛。体外感染HIV的单核细胞显示p35表达降低和p70产生减少,这表明这种IL-12表达的降低可能导致HIV阳性患者细胞中IL-12产生减少。此外,用IL-10处理细胞会增加HIV阳性和阴性细胞中IL-10 mRNA的表达,并降低p40的表达,而中和IL-10会增加p40 mRNA水平。这些观察结果,连同在HIV阳性患者中观察到的IL-10过度产生,可能解释了在HIV疾病中看到的IL-12产生的失调。