Roff Shannon R, Noon-Song Ezra N, Yamamoto Janet K
Department of Infectious Diseases and Pathology, College of Veterinary Medicine, University of Florida , Gainesville, FL , USA.
Front Immunol. 2014 Jan 13;4:498. doi: 10.3389/fimmu.2013.00498.
Interferon-γ (IFNγ) plays various roles in the pathogenesis of HIV/AIDS. In an HIV-1 infected individual, the production of IFNγ is detected as early as the acute phase and continually detected throughout the course of infection. Initially produced to clear the primary infection, IFNγ together with other inflammatory cytokines are involved in establishing a chronic immune activation that exacerbates clinical diseases associated with AIDS. Unlike Type 1 IFNs, IFNγ has no direct antiviral activity against HIV-1 in primary cultures, as supported by the in vivo findings of IFNγ therapy in infected subjects. Results from both in vitro and ex vivo studies show that IFNγ can instead enhance HIV-1 replication and its associated diseases, and therapies aimed at decreasing its production are under consideration. On the other hand, IFNγ has been shown to enhance cytotoxic T lymphocytes and NK cell activities against HIV-1 infected cells. These activities are important in controlling HIV-1 replication in an individual and will most likely play a role in the prophylaxis of an effective vaccine against HIV-1. Additionally, IFNγ has been used in combination with HIV-1 vaccine to augment antiviral immunity. Technological advancements have focused on using IFNγ as a biological marker to analyze the type(s) of immunity generated by candidate HIV vaccines and the levels of immunity restored by anti-retroviral drug therapies or novel immunotherapies. Hence, in addition to its valuable ancillary role as a biological marker for the development of effective HIV-1 prophylactic and therapeutic strategies, IFNγ has a vital role in promoting the pathogenesis of HIV.
干扰素-γ(IFNγ)在HIV/AIDS发病机制中发挥多种作用。在HIV-1感染个体中,早在急性期就能检测到IFNγ的产生,并且在整个感染过程中持续检测到。IFNγ最初产生是为了清除原发性感染,它与其他炎性细胞因子一起参与建立慢性免疫激活,从而加剧与艾滋病相关的临床疾病。与1型干扰素不同,在原代培养中,IFNγ对HIV-1没有直接抗病毒活性,这一点得到了感染受试者中IFNγ治疗的体内研究结果的支持。体外和离体研究结果均表明,IFNγ反而能增强HIV-1复制及其相关疾病,旨在降低其产生的治疗方法正在研究中。另一方面,IFNγ已被证明能增强细胞毒性T淋巴细胞和NK细胞对HIV-1感染细胞的活性。这些活性在控制个体中的HIV-1复制方面很重要,并且很可能在预防针对HIV-1的有效疫苗中发挥作用。此外,IFNγ已与HIV-1疫苗联合使用以增强抗病毒免疫力。技术进步集中在将IFNγ用作生物标志物,以分析候选HIV疫苗产生的免疫类型以及抗逆转录病毒药物疗法或新型免疫疗法恢复的免疫水平。因此,除了作为开发有效的HIV-1预防和治疗策略的生物标志物具有宝贵的辅助作用外,IFNγ在促进HIV发病机制方面也起着至关重要的作用。