Division of Immunology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, 4-4-1, Komatsushima, Aoba-ku, Sendai 981-8558, Japan.
Int Immunol. 2017 Jul 1;29(7):319-325. doi: 10.1093/intimm/dxx041.
Receptors for the Fc domain of immunoglobulins [Fc receptors (FcRs)] are essential for the maintenance of antibody-mediated immune responses. FcRs consist of activating- and inhibitory-type receptors that regulate adequate thresholds for various immune cells. In particular, polymorphisms and/or gene copy-number variations of FcRs for IgG (FcγRs) are closely associated with the development of inflammatory disorders, including autoimmune diseases. Recent evidence has implicated polymorphisms of FcRs in the efficacy of monoclonal antibody (mAb)-mediated therapy. This review provides an overview of genetic variations in human FcγRs and the clinical contribution of FcγR polymorphisms in mAb treatments for cancer, autoimmune diseases and allergies.
免疫球蛋白 Fc 结构域的受体(Fc 受体 (FcR))对于维持抗体介导的免疫反应至关重要。FcR 由激活型和抑制型受体组成,它们调节各种免疫细胞的适当阈值。特别是,FcγR(免疫球蛋白 G 的 Fc 受体)的 FcR 的多态性和/或基因拷贝数变异与炎症性疾病的发展密切相关,包括自身免疫性疾病。最近的证据表明,FcR 的多态性与单克隆抗体 (mAb) 介导的治疗效果有关。本综述概述了人类 FcγR 的遗传变异以及 FcγR 多态性在 mAb 治疗癌症、自身免疫性疾病和过敏中的临床贡献。