Caruso A, Canaris A D, Licenziati S, Cantalamessa A, Folghera S, Lonati M A, de Panfilis G, Garotta G, Turano A
Institute of Microbiology, University of Brescia, Italy.
J Acquir Immune Defic Syndr Hum Retrovirol. 1995 Dec 1;10(4):462-70. doi: 10.1097/00042560-199512000-00010.
Individual cells capable of interferon-gamma (IFN-gamma) synthesis are easily detected by immunofluorescence and flow cytometric analysis using an anti-IFN-gamma monoclonal antibody as specific reagent. By IFN-gamma flow cytometry assay, we demonstrated that HIV-seropositive patients, starting at the early stage of viral infection, generally have an increased percentage of lymphocytes potentially able to produce IFN-gamma, compared with healthy blood donors. IFN-gamma expression in patient lymphocytes was observed to increase with the progressive stages of HIV infection, with the highest figures occurring in stage C patients. Such increased IFN-gamma expression involved both CD4+ and CD8+ T cell subsets. Most interestingly, we found patients at the same stage of HIV infection who had similar numbers of total and CD4+ lymphocytes but highly different percentages of lymphocytes potentially capable of producing IFN-gamma.
使用抗γ干扰素(IFN-γ)单克隆抗体作为特异性试剂,通过免疫荧光和流式细胞术分析能够轻松检测出可合成IFN-γ的单个细胞。通过IFN-γ流式细胞术检测,我们发现,从病毒感染早期开始,与健康献血者相比,HIV血清阳性患者中潜在能够产生IFN-γ的淋巴细胞百分比普遍增加。观察到患者淋巴细胞中的IFN-γ表达随着HIV感染的进展阶段而增加,最高数值出现在C期患者中。这种IFN-γ表达的增加涉及CD4+和CD8+ T细胞亚群。最有趣的是,我们发现处于HIV感染同一阶段的患者,其总淋巴细胞和CD4+淋巴细胞数量相似,但潜在能够产生IFN-γ的淋巴细胞百分比却有很大差异。