Singer Benjamin D, King Landon S, D'Alessio Franco R
Division of Pulmonary and Critical Care Medicine, Johns Hopkins University , Baltimore, MD , USA.
Front Immunol. 2014 Feb 11;5:46. doi: 10.3389/fimmu.2014.00046. eCollection 2014.
Regulatory T cells (Tregs) suppress exuberant immune system activation and promote immunologic tolerance. Because Tregs modulate both innate and adaptive immunity, the biomedical community has developed an intense interest in using Tregs for immunotherapy. Conditions that require clinical tolerance to improve outcomes - autoimmune disease, solid organ transplantation, and hematopoietic stem cell transplantation - may benefit from Treg immunotherapy. Investigators have designed ex vivo strategies to isolate, preserve, expand, and infuse Tregs. Protocols to manipulate Treg populations in vivo have also been considered. Barriers to clinically feasible Treg immunotherapy include Treg stability, off-cell effects, and demonstration of cell preparation purity and potency. Clinical trials involving Treg adoptive transfer to treat graft versus host disease preliminarily demonstrated the safety and efficacy of Treg immunotherapy in humans. Future work will need to confirm the safety of Treg immunotherapy and establish the efficacy of specific Treg subsets for the treatment of immune-mediated disease.
调节性T细胞(Tregs)可抑制免疫系统的过度激活并促进免疫耐受。由于Tregs可调节先天性免疫和适应性免疫,生物医学界对使用Tregs进行免疫治疗产生了浓厚兴趣。需要临床耐受以改善预后的疾病——自身免疫性疾病、实体器官移植和造血干细胞移植——可能会从Treg免疫治疗中获益。研究人员已经设计了体外策略来分离、保存、扩增和注入Tregs。在体内操纵Treg群体的方案也已被考虑。临床可行的Treg免疫治疗的障碍包括Treg稳定性、非细胞效应以及细胞制剂纯度和效力的证明。涉及Treg过继转移治疗移植物抗宿主病的临床试验初步证明了Treg免疫治疗在人体中的安全性和有效性。未来的工作需要确认Treg免疫治疗的安全性,并确定特定Treg亚群治疗免疫介导疾病的疗效。