Deaprtment of Immunology and Serology, ICMR-National AIDS Research Institute, Pune, India.
Faculty of Health Sciences, Symbiosis International University (SIU), Pune, India.
Front Immunol. 2021 Apr 30;12:663919. doi: 10.3389/fimmu.2021.663919. eCollection 2021.
Persistence of HIV reservoir even in suppressive ART is the key obstacle in HIV-1 cure. We evaluated the ability of HIV-1 C Env to reactivate the latently infected resting memory CD4 cells and the ability of polyclonal HIV antibodies mediating ADCC to lyse the reactivated targets.
HIV-1 antibodies from 25 HIV infected individuals (14 ADCC responders and 11 non-responders) were tested against the Env-C reactivated primary cells; CD4+ and CD4+CD45RO+ memory T cells in the presence of autologous or heterologous effector cells using multicolor flow cytometry. The frequencies of p24+ve target cells were measured to determine the reactivation and antibody mediated lysis.
Increase in the frequency of p24 expressing cells (P < 0.01 in all cases) after Env-C stimulation of target cells indicated reactivation. When these reactivated targets were mixed with effector cells and HIV-1 antibodies, the frequencies of p24 expressing targets were decreased significantly when the ADCC mediating antibodies (P < 0.01 in all cases) were added but not when the antibodies from ADCC non-responders or HIV negative individuals were added. In parallel, the NK cell activation was also increased only when ADCC mediating antibodies were added.
The study showed that the HIV-1 Env could act as latency reversal agent (LRA), and only ADCC mediating antibodies could lyse the reactivated HIV reservoirs. The short stimulation cycle used in this study could be useful in testing LRAs as well as immune mediated lysis of reactivated reservoirs. The observations have further implication in designing antibody mediated immunotherapy for eradication of latent HIV reservoir.
即使在抑制性 ART 下,HIV 储库的持续存在也是 HIV-1 治愈的关键障碍。我们评估了 HIV-1 C Env 重新激活潜伏感染的静止记忆 CD4 细胞的能力,以及多克隆 HIV 抗体介导 ADCC 裂解重新激活靶标的能力。
用多色流式细胞术检测来自 25 名 HIV 感染者(14 名 ADCC 应答者和 11 名非应答者)的 HIV-1 抗体对 Env-C 重新激活的原代细胞的反应;在存在自体或异体细胞效应物的情况下,检测 CD4+和 CD4+CD45RO+记忆 T 细胞。测量 p24+ve 靶细胞的频率以确定重新激活和抗体介导的裂解。
目标细胞经 Env-C 刺激后 p24 表达细胞的频率增加(所有情况下均 P < 0.01)表明发生了重新激活。当这些重新激活的靶细胞与效应细胞和 HIV-1 抗体混合时,当添加 ADCC 介导的抗体时(所有情况下均 P < 0.01),p24 表达靶细胞的频率显著降低,但当添加 ADCC 非应答者或 HIV 阴性个体的抗体时则没有降低。同时,只有当添加 ADCC 介导的抗体时,NK 细胞的激活也增加。
该研究表明,HIV-1 Env 可以作为潜伏逆转剂(LRA),只有 ADCC 介导的抗体才能裂解重新激活的 HIV 储库。本研究中使用的短刺激周期可用于测试 LRA 以及重新激活储库的免疫介导裂解。这些观察结果对设计抗体介导的免疫疗法以消除潜伏的 HIV 储库具有进一步的意义。