Clinical Sciences Division, St. Michael's Hospital, University of Toronto, Canada.
J Immunol. 2010 Jul 1;185(1):498-506. doi: 10.4049/jimmunol.0903915. Epub 2010 Jun 2.
We examined the role of CD4(+) T cell IL-21 production in viral control of HIV infection. HIV-infected individuals had greater circulating IL-21-producing CD4(+) T cells in blood compared with uninfected volunteers. HIV-specific IL-21-producing CD4(+) T cells were detected in blood during untreated acute and chronic HIV infection, and elevated frequencies of these cells correlated with relative viral control. These cells had an effector memory or end effector phenotype and expressed CXCR5. HIV-specific CD8(+) T cells exhibited high levels of IL-21R, indicating sensitivity to IL-21. Low or aviremic long-term nonprogressors, however, showed absent or low HIV-specific IL-21 CD4(+) T cells, but more easily detectable HIV-specific IL-2-producing CD4(+) T cells, suggesting changing requirements for particular gamma-chain cytokines depending on Ag abundance. Thus, IL-21-producing CD4(+) T cells are induced in viremic HIV infection and likely contribute to viral control by affecting CD8(+) T cell maintenance.
我们研究了 CD4(+)T 细胞 IL-21 产生在 HIV 感染病毒控制中的作用。与未感染的志愿者相比,HIV 感染者血液中循环的产生 IL-21 的 CD4(+)T 细胞更多。在未经治疗的急性和慢性 HIV 感染期间,血液中检测到 HIV 特异性产生 IL-21 的 CD4(+)T 细胞,这些细胞的频率升高与相对病毒控制相关。这些细胞具有效应记忆或终末效应表型,并表达 CXCR5。HIV 特异性 CD8(+)T 细胞表现出高水平的 IL-21R,表明对 IL-21 敏感。然而,低病毒载量或长期非进展者表现出不存在或低水平的 HIV 特异性 IL-21 产生 CD4(+)T 细胞,但更易检测到 HIV 特异性产生 IL-2 的 CD4(+)T 细胞,这表明根据 Ag 丰度,特定 γ 链细胞因子的需求发生变化。因此,在病毒血症性 HIV 感染中诱导产生 IL-21 的 CD4(+)T 细胞,并可能通过影响 CD8(+)T 细胞的维持来有助于病毒控制。