Institute of Immunology and Immunotherapy, University of Birmingham, B15 2TT, United Kingdom.
Institute of Immunology and Immunotherapy, University of Birmingham, B15 2TT, United Kingdom.
Curr Opin Immunol. 2021 Jun;70:75-81. doi: 10.1016/j.coi.2021.03.019. Epub 2021 Apr 18.
Current treatments for autoimmune diseases do not address the immune pathology underlying their initiation and progression and too often rely on non-specific immunosuppressive drugs for control of symptoms. Antigen-specific immunotherapy aims to induce tolerance selectively among the cells causing the disease while leaving the rest of the adaptive immune system capable of protecting against infectious diseases and cancers. Here we describe how novel approaches for antigen-specific immunotherapy are designed to manipulate antigen presentation and promote tolerance to specific self-antigens. This analysis points to liver antigen presenting cells, targeted by carrier particles, and steady-state dendritic cells, to which antigen-processing independent T-cell epitopes (apitopes) bind directly, as the principal targets for antigen-specific immunotherapy. Delivery of antigens to these cells holds great promise for effective control of this rapidly expanding group of diseases.
目前针对自身免疫性疾病的治疗方法并不能解决其发病和进展的免疫病理学问题,而且往往依赖于非特异性免疫抑制剂来控制症状。抗原特异性免疫疗法旨在选择性诱导引起疾病的细胞产生耐受,同时使适应性免疫系统的其余部分能够预防传染病和癌症。在这里,我们描述了如何设计新型的抗原特异性免疫疗法来操纵抗原呈递并促进对特定自身抗原的耐受。该分析指出,肝脏抗原提呈细胞(被载体颗粒靶向)和稳态树突状细胞(抗原加工非依赖性 T 细胞表位(apitopes)直接结合的细胞)是抗原特异性免疫疗法的主要靶点。将抗原递送到这些细胞有望有效控制这一快速扩展的疾病群体。