VGTI Florida, Port St. Lucie, FL, USA.
Cytokine Growth Factor Rev. 2012 Aug-Oct;23(4-5):143-9. doi: 10.1016/j.cytogfr.2012.05.001. Epub 2012 Jun 27.
HIV persists in cellular and anatomical reservoirs during Highly Active Antiretroviral Therapy (HAART). In vitro studies as well as in vivo observations have identified cytokines as important factors regulating the immunological and virological mechanisms involved in HIV persistence. Immunosuppressive cytokines might contribute to the establishment of viral latency by dampening T cell activation and HIV production, thereby creating the necessary immuno-virological condition for the establishment of a pool of latently infected cells. Other cytokines that are involved in the maintenance of memory CD4(+) T cells promote the persistence of these cells during HAART. Conversely, proinflammatory cytokines may favor HIV persistence by exacerbating low levels of ongoing viral replication in lymphoid tissues even after prolonged therapy. The ability of several cytokines to interfere with the molecular mechanisms responsible for HIV latency makes them attractive candidates for therapeutic strategies aimed at reducing the pool of latently infected cells. In this article, we review the role of cytokines in HIV persistence during HAART and discuss their role as potential eradicating agents.
在高效抗逆转录病毒治疗(HAART)期间,HIV 存在于细胞和解剖学储库中。体外研究以及体内观察已经确定细胞因子是调节 HIV 持续存在所涉及的免疫和病毒学机制的重要因素。免疫抑制细胞因子可能通过抑制 T 细胞激活和 HIV 产生来促成病毒潜伏的建立,从而为潜伏感染细胞池的建立创造必要的免疫病毒学条件。其他参与记忆 CD4(+) T 细胞维持的细胞因子促进这些细胞在 HAART 期间的持续存在。相反,促炎细胞因子可能通过加剧淋巴组织中持续存在的低水平病毒复制,即使在长期治疗后,也有利于 HIV 的持续存在。几种细胞因子干扰 HIV 潜伏相关分子机制的能力使它们成为旨在减少潜伏感染细胞池的治疗策略的有吸引力的候选物。在本文中,我们综述了细胞因子在 HAART 期间 HIV 持续存在中的作用,并讨论了它们作为潜在清除剂的作用。