Department of Laboratory Medicine at the University of California, San Francisco, Calif.
Department of Surgery at the University of California, San Francisco, Calif.
J Allergy Clin Immunol. 2018 Dec;142(6):1710-1718. doi: 10.1016/j.jaci.2018.10.015. Epub 2018 Oct 25.
Forkhead box P3-expressing regulatory T (Treg) cells are essential for self-tolerance, with an emerging role in tissue repair and regeneration. Their ability to traffic to tissue and perform complex therapeutic tasks in response to the tissue microenvironment make them an attractive candidate for drug development. Early experiences of Treg cell therapy in patients with graft-versus-host disease, type 1 diabetes, and organ transplantation have shown that it is feasible, safe, and potentially efficacious in some settings. Many ongoing trials in patients with a wide variety of diseases will further enhance our knowledge about the optimal approaches for Treg cell manufacturing and dosing. We review the current preclinical rationale supporting Treg cell therapy in a variety of disease settings ranging from tissue transplantation, autoimmune diseases, and non-immune-mediated inflammatory settings. We point out challenges in development of Treg cell therapy and speculate how synthetic biology can be used to enhance the feasibility and efficacy of Treg cell therapy for autoimmune and autoinflammatory diseases.
叉头框蛋白 P3 表达的调节性 T(Treg)细胞对于自身耐受至关重要,并且在组织修复和再生中具有新兴作用。它们能够迁移到组织中,并根据组织微环境执行复杂的治疗任务,这使它们成为药物开发的有吸引力的候选者。在移植物抗宿主病、1 型糖尿病和器官移植患者中进行的 Treg 细胞治疗早期经验表明,在某些情况下,Treg 细胞治疗是可行、安全且潜在有效的。许多正在进行的针对各种疾病患者的试验将进一步增强我们对 Treg 细胞制造和剂量的最佳方法的了解。我们回顾了目前支持 Treg 细胞治疗在各种疾病环境中的临床前基本原理,包括组织移植、自身免疫性疾病和非免疫介导的炎症环境。我们指出了 Treg 细胞治疗发展中的挑战,并推测合成生物学如何用于增强 Treg 细胞治疗自身免疫和自身炎症性疾病的可行性和疗效。