aDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden bInserm, U955, Equipe 16, Créteil, France.
AIDS. 2013 Sep 24;27(15):2323-34. doi: 10.1097/QAD.0b013e328361a427.
A variety of B-cell dysfunctions are manifested during HIV-1 infection, as reported early during the HIV-1 epidemic. It is not unusual that the pathogenic mechanisms presented to elucidate impairment of B-cell responses during HIV-1 infection focus on the impact of reduced T-cell numbers and functions, and lack of germinal center formation in lymphoid tissues. To our understanding, however, perturbation of B-cell phenotype and function during HIV-1 infection may begin at several different B-cell developmental stages. These impairments can be mediated by intrinsic B-cell defects as well as by the lack of proper T-cell help. In this review, we will highlight some of the pathways and molecular interactions leading to B-cell impairment prior to germinal center formation and B-cell activation mediated through the B-cell receptor in response to HIV-1 antigens. Recent studies indicate a regulatory role for B cells on T-cell biology and immune responses. We will discuss some of these novel findings and how these regulatory mechanisms could potentially be affected by the intrinsic defects of B cells taking place during HIV-1 infection.
在 HIV-1 感染期间表现出多种 B 细胞功能障碍,这在 HIV-1 流行早期就有报道。在阐明 HIV-1 感染期间 B 细胞反应受损的致病机制时,通常集中在 T 细胞数量和功能减少以及淋巴组织中缺乏生发中心形成上,这并不罕见。然而,据我们所知,HIV-1 感染期间 B 细胞表型和功能的紊乱可能始于几个不同的 B 细胞发育阶段。这些损伤可以通过 B 细胞内在缺陷以及缺乏适当的 T 细胞辅助来介导。在这篇综述中,我们将重点介绍一些导致生发中心形成之前 B 细胞受损的途径和分子相互作用,以及通过 B 细胞受体对 HIV-1 抗原的反应介导的 B 细胞激活。最近的研究表明 B 细胞在 T 细胞生物学和免疫反应中具有调节作用。我们将讨论其中一些新发现,以及这些调节机制如何可能受到 HIV-1 感染期间 B 细胞内在缺陷的影响。