Peakman Mark, Santamaria Pere
Immunology and Inflammation Research Therapeutic Area, Sanofi, Cambridge, Massachusetts 02141, USA
Department of Microbiology, Immunology and Infectious Diseases, Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Alberta T2N 4N1, Canada
Cold Spring Harb Perspect Med. 2025 Jun 2;15(6):a041598. doi: 10.1101/cshperspect.a041598.
Type 1 diabetes (T1D) is driven by an immunologically complex, diverse, and self-sustaining immune response directed against tissue autoantigens, leading to loss or dysfunction of β cells. To date, the single approved immune intervention in T1D is based on a strategy that is similar to that used in other related autoimmune diseases, namely, the attenuation of immune cell activation. As a next-generation approach that is more focused on underlying mechanisms of loss of tolerance, antigen-specific immunotherapy is designed to establish or restore bystander immunoregulation in a highly tissue- and target-specific fashion. Here, we describe the basis for this alternative approach, which could also have potential for complementarity if used in combination with more conventional immune modulators, and highlight recent advances, knowledge gaps, and next steps in clinical development.
1型糖尿病(T1D)是由针对组织自身抗原的免疫复杂、多样且自我维持的免疫反应驱动的,导致β细胞丧失或功能障碍。迄今为止,T1D中唯一获批的免疫干预措施是基于一种与其他相关自身免疫性疾病所采用的策略类似的方法,即减弱免疫细胞激活。作为一种更关注耐受性丧失潜在机制的下一代方法,抗原特异性免疫疗法旨在以高度组织和靶点特异性的方式建立或恢复旁观者免疫调节。在此,我们描述了这种替代方法的基础,如果与更传统的免疫调节剂联合使用,该方法也可能具有互补潜力,并强调了临床开发中的最新进展、知识空白和下一步措施。