MRC Centre for Transplantation, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Clin Exp Immunol. 2013 May;172(2):158-68. doi: 10.1111/cei.12052.
Transplantation is a successful treatment for end-stage organ failure. Despite improvements in short-term outcome, long-term survival remains suboptimal because of the morbidity and mortality associated with long-term use of immunosuppression. There is, therefore, a pressing need to devise protocols that induce tolerance in order to minimize or completely withdraw immunosuppression in transplant recipients. In this review we will discuss how regulatory T cells (T(regs)) came to be recognized as an attractive way to promote transplantation tolerance. We will summarize the preclinical data, supporting the importance of these cells in the induction and maintenance of immune tolerance and that provide the rationale for the isolation and expansion of these cells for cellular therapy. We will also describe the data from the first clinical trials, using T(regs) to inhibit graft-versus-host disease (GVHD) after haematopoietic stem cell transplantation and will address both the challenges and opportunities in human T(reg) cell therapy.
移植是治疗终末期器官衰竭的一种成功疗法。尽管短期结果有所改善,但由于长期使用免疫抑制相关的发病率和死亡率,长期存活率仍然不理想。因此,迫切需要制定诱导耐受的方案,以便最大限度地减少或完全撤回移植受者的免疫抑制。在这篇综述中,我们将讨论调节性 T 细胞(Tregs)如何被认为是促进移植耐受的一种有吸引力的方法。我们将总结支持这些细胞在诱导和维持免疫耐受中的重要性的临床前数据,并为分离和扩增这些细胞进行细胞治疗提供依据。我们还将描述造血干细胞移植后使用 Tregs 抑制移植物抗宿主病(GVHD)的首次临床试验数据,并讨论人 Treg 细胞治疗中的挑战和机遇。