Tolerance regeneration by T regulatory cells in autologous haematopoietic stem cell transplantation for autoimmune diseases

被引:6
|
作者
Hendrawan, Kevin [1 ,2 ,3 ]
Visweswaran, Malini [1 ,3 ]
Ma, David D. F. [1 ,2 ,3 ]
Moore, John J. [1 ,2 ,3 ]
机构
[1] St Vincents Ctr Appl Med Res, Blood Stem Cells & Canc Res Programme, Darlinghurst, NSW 2011, Australia
[2] Univ New South Wales, Fac Med, St Vincents Clin Sch, Sydney, NSW 2010, Australia
[3] St Vincents Hosp, Dept Haematol, Darlinghurst, NSW 2010, Australia
基金
英国医学研究理事会;
关键词
IMMUNOLOGICAL SELF-TOLERANCE; REMITTING MULTIPLE-SCLEROSIS; SYSTEMIC-SCLEROSIS; SUPPRESSIVE FUNCTION; PERIPHERAL-BLOOD; EXPRESSION; CD39; FOXP3; TH17; NAIVE;
D O I
10.1038/s41409-019-0710-2
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Autologous haematopoietic stem cell transplantation shows increasing promise as a therapeutic option for patients with treatment-refractory autoimmune disease, particularly systemic sclerosis and multiple sclerosis. However, this intensive chemotherapy-based procedure is not always possible due to potential treatment toxicities and comorbidities. The biological mechanisms of how this procedure induces long-term remission in autoimmune disease are increasingly understood. The focus of this review is on recent research findings on the role of CD4+ T regulatory cells (Tregs) in resetting the immune system leading to the eradication of the autoimmune disease after transplantation. Discovery of the precise mechanisms of this process will allow development of novel Treg-based therapies and thus avoid the need for intensive chemotherapy-based treatment for these autoimmune diseases in the future.
引用
收藏
页码:857 / 866
页数:10
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