Riviere-Cazaux Cecile, Cornell Jessica, Shen Yang, Zhou Miou
Graduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA, USA.
Mayo Clinic Alix School of Medicine, Rochester, MN, USA.
Heliyon. 2022 Jul 14;8(7):e09950. doi: 10.1016/j.heliyon.2022.e09950. eCollection 2022 Jul.
While combination antiretroviral therapy (cART) has successfully increased the lifespan of individuals infected with HIV, a significant portion of this population remains affected by HIV-associated neurocognitive disorder (HAND). C-C chemokine receptor 5 (CCR5) has been well studied in immune response and as a co-receptor for HIV infection. HIV-infected (HIV) patients experienced mild to significant amelioration of cognitive function when treated with different CCR5 antagonists, including maraviroc and cenicriviroc. Consistent with clinical results, knockout or knockdown rescued cognitive deficits in HIV animal models, with mechanisms of reduced microgliosis and neuroinflammation. Pharmacologic inhibition of CCR5 directly improved cerebral and hippocampal neuronal plasticity and cognitive function. By summarizing the animal and human studies of CCR5 in HIV-associated cognitive deficits, this review aims to provide an overview of the mechanistic role of CCR5 in HAND pathophysiology. This review also discusses the addition of CCR5 antagonists, such as maraviroc, to cART for targeted prevention and treatment of cognitive impairments in patients infected with HIV.
虽然联合抗逆转录病毒疗法(cART)成功延长了HIV感染者的寿命,但该人群中很大一部分仍受到HIV相关神经认知障碍(HAND)的影响。C-C趋化因子受体5(CCR5)在免疫反应以及作为HIV感染的共受体方面已得到充分研究。接受包括马拉维若和塞尼卡维若在内的不同CCR5拮抗剂治疗时,HIV感染(HIV)患者的认知功能有轻度到显著改善。与临床结果一致,在HIV动物模型中,CCR5基因敲除或敲低可挽救认知缺陷,其机制是小胶质细胞增生和神经炎症减轻。CCR5的药理学抑制直接改善了大脑和海马神经元的可塑性以及认知功能。通过总结CCR5在HIV相关认知缺陷方面的动物和人体研究,本综述旨在概述CCR5在HAND病理生理学中的机制作用。本综述还讨论了在cART中添加CCR5拮抗剂(如马拉维若)以针对性预防和治疗HIV感染患者认知障碍的问题。