Ramlal Reshma, Hildebrandt Gerhard C
Division of Hematology and Bone Marrow Transplantation, University of Kentucky, Markey Cancer Center 800 Rose Street, Lexington, KY 40536, USA.
Biomedicines. 2017 May 16;5(2):23. doi: 10.3390/biomedicines5020023.
Regulatory T (Tregs) cells play a crucial role in immunoregulation and promotion of immunological tolerance. Adoptive transfer of these cells has therefore been of interest in the field of bone marrow and solid organ transplantation, autoimmune diseases and allergy medicine. In bone marrow transplantation, Tregs play a pivotal role in the prevention of graft-verus-host disease (GvHD). This has generated interest in using adoptive Treg cellular therapy in the prevention and treatment of GvHD. There have been several barriers to the feasibility of Treg cellular therapy in the setting of hematopoietic stem cell transplantation (HSCT) which include low Treg concentration in peripheral blood, requiring expansion of the Treg population; instability of the expanded product with loss of FoxP3 expression; and issues related to the purity of the expanded product. Despite these challenges, investigators have been able to successfully expand these cells both in vivo and in vitro and have demonstrated that they can be safely infused in humans for the prevention and treatment of GvHD with no increase in relapse risk or infections risk.
调节性T(Tregs)细胞在免疫调节和促进免疫耐受中发挥着关键作用。因此,这些细胞的过继转移在骨髓和实体器官移植、自身免疫性疾病及变态反应医学领域备受关注。在骨髓移植中,Tregs在预防移植物抗宿主病(GvHD)方面起着关键作用。这引发了人们对采用Treg细胞疗法预防和治疗GvHD的兴趣。在造血干细胞移植(HSCT)背景下,Treg细胞疗法的可行性存在若干障碍,包括外周血中Treg浓度低,需要扩增Treg群体;扩增产物不稳定,FoxP3表达丧失;以及与扩增产物纯度相关的问题。尽管存在这些挑战,研究人员已能够在体内和体外成功扩增这些细胞,并证明它们可以安全地输注给人类以预防和治疗GvHD,且不会增加复发风险或感染风险。