Research & Development, Cour Pharmaceuticals Development Company, Northbrook, IL, USA; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Research & Development, Cour Pharmaceuticals Development Company, Northbrook, IL, USA; Department of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Nanomedicine. 2019 Jun;18:282-291. doi: 10.1016/j.nano.2018.10.001. Epub 2018 Oct 21.
Autoimmune diseases, such as celiac disease, multiple sclerosis, and type 1 diabetes, are leading causes of morbidity and mortality in the United States. In these disease states, immune regulatory mechanisms fail that result in T and B cell-mediated destruction of self-tissues. The known role of T cells in mediating autoimmune diseases has led to the emergence of numerous therapies aimed at inactivating T cells, however successful 'tolerance-inducing' strategies have not yet emerged for approved standard-of-care clinical use. In this review, we describe relevant examples of antigen-specific tolerance approaches that have been applied in clinical trials for human diseases. Furthermore, we describe the evolution of biomaterial approaches from cell-based therapies to induce immune tolerance with a focus on the Tolerogenic Immune-Modifying nanoParticle (TIMP) platform. The TIMP platform can be designed to treat various autoimmune conditions and is currently in clinical trials testing its ability to reverse celiac disease.
自身免疫性疾病,如乳糜泻、多发性硬化症和 1 型糖尿病,是美国发病率和死亡率的主要原因。在这些疾病状态下,免疫调节机制失效,导致 T 和 B 细胞介导的自身组织破坏。T 细胞在介导自身免疫性疾病中的已知作用导致了许多旨在使 T 细胞失活的治疗方法的出现,然而,成功的“诱导耐受”策略尚未出现,也未被批准用于标准的临床应用。在这篇综述中,我们描述了已应用于人类疾病临床试验的抗原特异性耐受方法的相关实例。此外,我们描述了从基于细胞的疗法发展到诱导免疫耐受的生物材料方法,重点介绍了免疫调节纳米颗粒(TIMP)平台。TIMP 平台可用于治疗各种自身免疫性疾病,目前正在临床试验中测试其逆转乳糜泻的能力。