Reitano K N, Kottilil S, Gille C M, Zhang X, Yan M, O'Shea M A, Roby G, Hallahan C W, Yang J, Lempicki R A, Arthos J, Fauci A S
Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health/DHHS, SAIC-Frederick, NCI, Frederick, MD 21702, USA.
AIDS Res Hum Retroviruses. 2009 Oct;25(10):1029-37. doi: 10.1089/aid.2008.0311.
HIV viremia is associated with a wide range of immune dysfunctions that contribute to the immunocompromised state. HIV viremia has been shown to have a broad effect on several immune cell types and/or their interactions that are vital for mounting an effective immune response. In this study, we investigated the integrity of plasmacytoid dendritic cell (pDC)-NK cell interactions among HIV viremic, aviremic, and seronegative individuals. We describe a critical defect in the ability of pDCs from HIV-infected individuals to secrete IFN-alpha and TNF and subsequently activate NK cells. We also describe an inherent defect on NK cells from HIV-infected individuals to respond to pDC-secreted cytokines. Furthermore, we were able to demonstrate a direct effect of HIV trimeric gp120 on NK cells in vitro similar to that described ex vivo. Finally, we were able to establish that the HIV gp120-mediated suppressive effect on NK cells was a result of its binding to the integrin alpha(4)beta(7) expressed on NK cells. These findings suggest a novel mechanism by which HIV is capable of suppressing an innate immune function in infected individuals.
HIV病毒血症与多种免疫功能障碍相关,这些功能障碍导致免疫功能受损状态。已表明HIV病毒血症对几种免疫细胞类型和/或它们之间的相互作用具有广泛影响,而这些对于产生有效的免疫反应至关重要。在本研究中,我们调查了HIV病毒血症患者、无病毒血症患者和血清阴性个体中浆细胞样树突状细胞(pDC)-NK细胞相互作用的完整性。我们描述了HIV感染个体的pDC分泌IFN-α和TNF并随后激活NK细胞能力的关键缺陷。我们还描述了HIV感染个体的NK细胞对pDC分泌的细胞因子作出反应的内在缺陷。此外,我们能够在体外证明HIV三聚体gp120对NK细胞有直接作用,类似于在体内所描述的那样。最后,我们能够确定HIV gp120对NK细胞的抑制作用是其与NK细胞上表达的整合素α(4)β(7)结合的结果。这些发现提示了一种HIV能够抑制感染个体先天免疫功能的新机制。