Department of Oncology, University of Oxford, Oxford, United Kingdom.
The Jackson Laboratory, Bar Harbor, ME, United States.
Front Immunol. 2023 Feb 22;14:1096759. doi: 10.3389/fimmu.2023.1096759. eCollection 2023.
The human immunodeficiency virus (HIV) is still a global pandemic and despite the successful use of anti-retroviral therapy, a well-established cure remains to be identified. Viral modulation of cell death has a significant role in HIV pathogenesis. Here we sought to understand the major mechanisms of HIV-induced death of lymphocytes and the effects on viral transmission. Flow cytometry analysis of lymphocytes from five latent HIV-infected patients, and HIV IIIB-infected MT2 cells demonstrated both necrosis and apoptosis to be the major mechanisms of cell death in CD4 and CD4/CD8 lymphocytes. Significantly, pro-apoptotic tumor necrosis factor (TNF) peptide (P13) was found to inhibit HIV-related cell death and reduced viral transmission. Whereas pro-necrotic TNF peptide (P16) had little effect on HIV-related cell death and viral transmission. Understanding mechanisms by which cell death can be manipulated may provide additional drug targets to reduce the loss of CD4 cells and the formation of a viral reservoir in HIV infection.
人类免疫缺陷病毒 (HIV) 仍然是一种全球大流行疾病,尽管抗逆转录病毒疗法取得了成功,但仍有待确定有效的治愈方法。病毒对细胞死亡的调节在 HIV 发病机制中起着重要作用。在这里,我们试图了解 HIV 诱导淋巴细胞死亡的主要机制及其对病毒传播的影响。对来自 5 名潜伏性 HIV 感染患者和 HIV IIIB 感染的 MT2 细胞的淋巴细胞进行流式细胞术分析表明,细胞坏死和细胞凋亡都是 CD4 和 CD4/CD8 淋巴细胞死亡的主要机制。值得注意的是,发现促凋亡肿瘤坏死因子 (TNF) 肽 (P13) 可抑制与 HIV 相关的细胞死亡并降低病毒传播。而促坏死 TNF 肽 (P16) 对与 HIV 相关的细胞死亡和病毒传播几乎没有影响。了解细胞死亡如何被操纵的机制可能为减少 HIV 感染中 CD4 细胞的损失和形成病毒储存库提供额外的药物靶点。