IrsiCaixa AIDS Research Institute, Hospital Germans Trias i Pujol, Institute for Health Science Research Germans Trias i Pujol (IGTP), Badalona, Spain.
Departament de Biologia Cellular, de Fisiologia i d'Immunologia, Universitat Autonoma de Barcelona, Cerdanyola del Valles, Spain.
Front Immunol. 2022 Jun 15;13:928039. doi: 10.3389/fimmu.2022.928039. eCollection 2022.
T cell responses are considered critical for the control of HIV, but the contribution of different T cell subsets to this control remains unclear. Using a boosted flow cytometric approach that is able to differentiate CD4 and CD8 T cell Th1/Tc1, Th2/Tc2, Th17/Tc17, Treg and Tfh/Tfc-like HIV-specific T cell populations, we identified CD8 Tfc responses that were related to HIV plasma viral loads and associated with rate of antibody isotype class switching to IgG. This favorable balance towards IgG responses positively correlated with increased virus neutralization, higher avidity of neutralizing antibodies and more potent antibody-dependent cell cytotoxicity (ADCC) in PBMCs from HIV controllers compared to non-controllers. Our results identified the CD8 Tfc-like T-cell response as a component of effective virus control which could possibly be exploited therapeutically.
T 细胞应答被认为对 HIV 的控制至关重要,但不同 T 细胞亚群对此控制的贡献仍不清楚。本研究采用增强型流式细胞术,能够区分 CD4 和 CD8 T 细胞 Th1/Tc1、Th2/Tc2、Th17/Tc17、Treg 和 Tfh/Tfc 样 HIV 特异性 T 细胞群,我们发现 CD8 Tfc 应答与 HIV 血浆病毒载量相关,并与抗体同种型类别转换为 IgG 的速率相关。与非控制者相比,HIV 控制者的 PBMC 中,这种有利于 IgG 应答的平衡与增加的病毒中和作用、更高的中和抗体亲和力和更有效的抗体依赖性细胞细胞毒性(ADCC)呈正相关。我们的研究结果确定了 CD8 Tfc 样 T 细胞应答是有效病毒控制的组成部分,这可能具有治疗潜力。