HIV & Immunology Division, Department of Microbiology, All India Institute of Medical Sciences, New Delhi, India.
Cytokine. 2012 Oct;60(1):55-63. doi: 10.1016/j.cyto.2012.06.288. Epub 2012 Jul 26.
Th17 cells play a crucial role in host immune response. We examined the role of Th17 cells in HIV-1 'subtype-C' infection and report that HIV-1 specific Th17 cells are induced in early infection and slow progressors but are significantly reduced at late stage of infection. There was a further decline in Th17 cells in late stage subjects with gastrointestinal infections. Additionally, we observed expanded population of IL-21 (needed for Th17 population expansion) producing CD4 T cells in early and slow progressors compared to subjects with late stage infection. A significant positive correlation existed between virus specific IL-17 and IL-21 producing CD4 T cells suggesting that HIV-1 infection induces a demand for Th17 cells. A significant negative correlation between virus specific Th17 cells and HIV-1 plasma viral load (pVL) was also observed, indicating a gradual loss of Th17 cells with HIV-1 disease progression.
辅助性 T 细胞 17(Th17 细胞)在宿主免疫反应中起着至关重要的作用。我们研究了 Th17 细胞在人类免疫缺陷病毒 1 型(HIV-1)“亚型-C”感染中的作用,结果表明在早期感染和疾病进展缓慢的患者中诱导了 HIV-1 特异性 Th17 细胞,但在感染晚期,这些细胞的数量明显减少。在晚期合并胃肠道感染的患者中,Th17 细胞进一步减少。此外,与晚期感染患者相比,我们观察到早期和疾病进展缓慢的患者中,IL-21(Th17 细胞扩增所必需的)产生的 CD4 T 细胞的群体扩张。HIV-1 特异性 IL-17 和 IL-21 产生的 CD4 T 细胞之间存在显著的正相关,表明 HIV-1 感染诱导了对 Th17 细胞的需求。HIV-1 特异性 Th17 细胞与 HIV-1 血浆病毒载量(pVL)之间也存在显著的负相关,表明随着 HIV-1 疾病的进展,Th17 细胞逐渐丢失。