Reka S, Garro M L, Kotler D P
Department of Medicine, St. Luke's-Roosevelt Hospital Center, College of Physicians and Surgeons, Columbia University, New York.
Lymphokine Cytokine Res. 1994 Dec;13(6):391-8.
Previous studies demonstrated that mucosal HIV p24 antigen content varied during the progression of HIV infection. In this study, expression of HIV RNA and mRNA of selected cytokines was examined in rectal mucosa from HIV-infected individuals. Rectal biopsies from 27 subjects were studied: 7 with CD4 counts > 500/mm3 (early), 11 with CD4 < 500 (intermediate), and 9 with AIDS (late), plus 4 HIV-seronegative controls. RNA in situ hybridization was performed using 35S-labeled riboprobes of HIV, TNF-alpha, IL-1 beta, IL-2, IL-4, IL-5, IL-6, IL-10, INF-alpha, IFN-gamma, and TGF-beta. HIV RNA was detected more frequently in the intermediate group than in the other groups (p < 0.005). Cytokine mRNA expression also varied during disease progression. The expression of IFN-alpha, IFN-gamma, and TGF-beta mRNA was most prevalent early in the disease; peak expression of IL-4, IL-5, IL-6, and IL-10 was seen during the intermediate stage, and peak expression of TNF-alpha and IL-1 beta mRNA were seen in AIDS patients. HIV RNA and cytokine mRNA expression vary during HIV disease progression. HIV RNA expression is greatest in the intermediate stage of the disease. The pattern of cytokine mRNA expression suggests predominant cell-mediated immunity under basal conditions and early in the disease, generalized cytokine activation in its middle phase, and proinflammatory cytokine activation in AIDS patients. Cytokine modulation of HIV expression in rectal mucosa in vivo may occur and have pathogenic importance.
先前的研究表明,在HIV感染的进展过程中,黏膜HIV p24抗原含量会发生变化。在本研究中,对HIV感染者直肠黏膜中HIV RNA及选定细胞因子的mRNA表达进行了检测。研究了27名受试者的直肠活检样本:7名CD4细胞计数>500/mm³(早期),11名CD4<500(中期),9名患有艾滋病(晚期),外加4名HIV血清阴性对照。使用35S标记的HIV、TNF-α、IL-1β、IL-2、IL-4、IL-5、IL-6、IL-10、INF-α、IFN-γ和TGF-β核糖探针进行RNA原位杂交。HIV RNA在中期组中的检测频率高于其他组(p<0.005)。细胞因子mRNA表达在疾病进展过程中也有所不同。IFN-α、IFN-γ和TGF-β mRNA的表达在疾病早期最为普遍;IL-4、IL-5、IL-6和IL-10的表达高峰出现在中期,而TNF-α和IL-1β mRNA的表达高峰出现在艾滋病患者中。HIV RNA和细胞因子mRNA表达在HIV疾病进展过程中会发生变化。HIV RNA表达在疾病中期最高。细胞因子mRNA表达模式表明,在基础条件下和疾病早期主要是细胞介导的免疫,在中期是全身性细胞因子激活,在艾滋病患者中是促炎细胞因子激活。体内直肠黏膜中细胞因子对HIV表达的调节可能会发生并具有致病重要性。