Macatangay Bernard Jc, Rinaldo Charles R
HIV/AIDS Program, Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
HIV Ther. 2010 Nov;4(6):639-647. doi: 10.2217/hiv.10.51.
Significant research has been conducted on the role of regulatory T cells (Tregs) in HIV infection. To date, however, it is not clear whether Tregs play a detrimental role or a beneficial role in the pathogenesis of HIV infection. In fact, a number of immunotherapeutic strategies to control HIV infection have revealed a possible antagonistic role for Tregs. This necessitates investigating ways to counteract the suppressive function, such as through Treg depletion or blockade of specific Treg immunosuppressive mechanisms, without further increasing the cellular immune activation associated with chronic HIV infection. Simply applying Treg immunotherapeutic strategies used in diseases other than HIV may pose problems due to the complexity of HIV immunopathogenesis. Studies are therefore necessary to elucidate the different immunoregulatory networks in HIV infection in order to determine the specific cellular or molecular pathways that can be altered to boost the body's immune control of HIV.
关于调节性T细胞(Tregs)在HIV感染中的作用,已经开展了大量研究。然而,迄今为止,尚不清楚Tregs在HIV感染发病机制中是发挥有害作用还是有益作用。事实上,一些控制HIV感染的免疫治疗策略已揭示出Tregs可能具有拮抗作用。这就需要研究对抗其抑制功能的方法,例如通过清除Tregs或阻断特定的Treg免疫抑制机制,同时又不会进一步增加与慢性HIV感染相关的细胞免疫激活。由于HIV免疫发病机制的复杂性,简单应用用于HIV以外疾病的Treg免疫治疗策略可能会带来问题。因此,有必要开展研究以阐明HIV感染中不同的免疫调节网络,从而确定可以改变哪些特定的细胞或分子途径来增强机体对HIV的免疫控制。