Hawaii Center for AIDS, John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii 96816, USA.
J Leukoc Biol. 2010 Apr;87(4):621-6. doi: 10.1189/jlb.0809571. Epub 2010 Feb 3.
It is broadly accepted that HIV DNA in lymphoid and myeloid cells persists despite combination antiretroviral therapy. Recognized as the Achilles heel to HIV eradication, the role of these peripheral reservoirs in HIV morbidity is less well developed. The burden of HIV DNA in peripheral mononuclear cells is linked to HIV disease outcomes such as time to AIDS diagnosis, survival, and CD4 T-lymphocyte counts. Monocytes are a minor HIV DNA reservoir, and the burden of HIV DNA in these cells appears to be linked to dementia, suggesting that residual infection in this subset is linked to tissue-related HIV complications. Since monocytes are likely involved in trafficking virus to the brain, there is a strong mechanistic link underlying this discovery. Herein, we summarize our current understanding of monocyte HIV DNA and central nervous system dysfunction in humans. We present a model to understand these relationships and suggest possible treatment approaches to be tested.
人们普遍认为,尽管采用了联合抗逆转录病毒疗法,淋巴样和髓样细胞中的 HIV DNA 仍会持续存在。这些外周储库被认为是 HIV 根除的致命弱点,但其在 HIV 发病机制中的作用尚不清楚。外周单核细胞中的 HIV DNA 负担与 HIV 疾病结局相关,如艾滋病诊断时间、存活时间和 CD4 淋巴细胞计数。单核细胞是 HIV DNA 的次要储存库,这些细胞中的 HIV DNA 负担似乎与痴呆症有关,这表明该亚群中残留的感染与与组织相关的 HIV 并发症有关。由于单核细胞可能参与将病毒贩运到大脑,因此在这一发现背后存在着很强的机制联系。本文总结了我们目前对人类单核细胞 HIV DNA 和中枢神经系统功能障碍的认识。我们提出了一个模型来理解这些关系,并提出了一些可能的治疗方法来进行测试。