Department of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Department of Infectious Diseases, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
J Immunol Res. 2021 Sep 29;2021:7316456. doi: 10.1155/2021/7316456. eCollection 2021.
Although antiretroviral therapy effectively controls human immunodeficiency virus (HIV) replication, a residual chronic immune activation/inflammation persists throughout the disease. This aberrant immune activation and inflammation are considered an accelerator of non-AIDS-related events and one of the driving forces of CD4 T cell depletion. Unfortunately, HIV-associated immune activation is driven by various factors, while the mechanism of excessive inflammation has not been formally clarified. To date, several clinical interventions or treatment candidates undergoing clinical trials have been proposed to combat this systemic immune activation/inflammation. However, these strategies revealed limited results, or their nonspecific anti-inflammatory properties are similar to previous interventions. Here, we reviewed recent learnings of immune activation and persisting inflammation associated with HIV infection, as well as the current directions to overcome it. Of note, a more profound understanding of the specific mechanisms for aberrant inflammation is still imperative for identifying an effective clinical intervention strategy.
虽然抗逆转录病毒疗法可有效控制人类免疫缺陷病毒 (HIV) 的复制,但在整个疾病过程中仍存在持续的慢性免疫激活/炎症。这种异常的免疫激活和炎症被认为是加速非艾滋病相关事件的因素之一,也是 CD4 T 细胞耗竭的驱动力之一。不幸的是,HIV 相关的免疫激活是由多种因素驱动的,而过度炎症的机制尚未得到正式阐明。迄今为止,已经提出了几种正在临床试验中进行的临床干预或治疗候选药物来对抗这种全身免疫激活/炎症。然而,这些策略的结果有限,或者它们的非特异性抗炎特性与以前的干预措施相似。在这里,我们回顾了与 HIV 感染相关的免疫激活和持续炎症的最新研究进展,以及克服这些问题的当前方向。值得注意的是,更深入地了解异常炎症的具体机制对于确定有效的临床干预策略仍然至关重要。