Raïch-Regué Dalia, Glancy Megan, Thomson Angus W
Starzl Transplantation Institute, Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Starzl Transplantation Institute, Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA; Department of Immunology, University of Pittsburgh, Pittsburgh, PA, USA; Clinical and Translational Science Institute, University of Pittsburgh, Pittsburgh, PA, USA.
Immunol Lett. 2014 Oct;161(2):216-21. doi: 10.1016/j.imlet.2013.11.016. Epub 2013 Dec 4.
Dendritic cells (DC) are highly-specialized, bone marrow-derived antigen-presenting cells that induce or regulate innate and adaptive immunity. Regulatory or "tolerogenic" DC play a crucial role in maintaining self tolerance in the healthy steady-state. These regulatory innate immune cells subvert naïve or memory T cell responses by various mechanisms. Regulatory DC (DCreg) also exhibit the ability to induce or restore T cell tolerance in many animal models of autoimmune disease or transplant rejection. There is also evidence that adoptive transfer of DCreg can regulate T cell responses in non-human primates and humans. Important insights gained from in vitro studies and animal models have led recently to the development of clinical grade human DCreg, with potential to treat autoimmune disease or enhance transplant survival while reducing patient dependency on immunosuppressive drugs. Phase I trials have been conducted in type-1 diabetes and rheumatoid arthritis, with results that emphasize the feasibility and safety of DCreg therapy. This mini-review will outline how observations made using animal models have been translated into human use, and discuss the challenges faced in further developing this form of regulatory immune cell therapy in the fields of autoimmunity and transplantation.
树突状细胞(DC)是高度专业化的、源自骨髓的抗原呈递细胞,可诱导或调节先天性免疫和适应性免疫。调节性或“耐受性”DC在健康稳态下维持自身耐受性方面发挥着关键作用。这些调节性先天性免疫细胞通过多种机制破坏幼稚或记忆性T细胞反应。在许多自身免疫性疾病或移植排斥的动物模型中,调节性DC(DCreg)也表现出诱导或恢复T细胞耐受性的能力。也有证据表明,DCreg的过继转移可调节非人灵长类动物和人类的T细胞反应。最近,从体外研究和动物模型中获得的重要见解促使了临床级人DCreg的开发,其有可能治疗自身免疫性疾病或提高移植存活率,同时减少患者对免疫抑制药物的依赖。I期试验已在1型糖尿病和类风湿性关节炎中进行,结果强调了DCreg疗法的可行性和安全性。本综述将概述如何将利用动物模型所取得的观察结果转化为人类应用,并讨论在自身免疫和移植领域进一步开发这种调节性免疫细胞疗法所面临的挑战。