Department of Immunology & Microbiology, University of Colorado School of Medicine, Aurora, CO 80045, United States.
Department of Immunology & Microbiology, University of Colorado School of Medicine, Aurora, CO 80045, United States.
Curr Opin Immunol. 2017 Aug;47:26-34. doi: 10.1016/j.coi.2017.06.004. Epub 2017 Jul 17.
HIV-1 infection typically eludes antibody control by our immune system and is not yet prevented by a vaccine. While many viral features contribute to this immune evasion, broadly neutralizing antibodies (bnAbs) against HIV-1 are often autoreactive and it has been suggested that immunological tolerance may restrict a neutralizing antibody response. Indeed, recent Ig knockin mouse studies have shown that bnAb-expressing B cells are largely censored by central tolerance in the bone marrow. However, the contribution of peripheral tolerance in limiting the HIV antibody response by anergic and potentially protective B cells is poorly understood. Studies using mouse models to elucidate how anergic B cells are regulated and can be recruited into HIV-specific neutralizing antibody responses may provide insight into the development of a protective HIV-1 vaccine.
HIV-1 感染通常能逃避我们免疫系统的抗体控制,目前还无法通过疫苗来预防。虽然许多病毒特征有助于这种免疫逃避,但针对 HIV-1 的广泛中和抗体 (bnAb) 通常具有自身反应性,有人认为免疫耐受可能会限制中和抗体反应。事实上,最近的 Ig 基因敲入小鼠研究表明,bnAb 表达 B 细胞在很大程度上受到骨髓中中枢耐受的抑制。然而,外周耐受在限制无反应性和潜在保护性 B 细胞的 HIV 抗体反应方面的作用还知之甚少。使用小鼠模型研究阐明无反应性 B 细胞是如何受到调节的,并能被招募到 HIV 特异性中和抗体反应中,可能有助于深入了解保护性 HIV-1 疫苗的开发。