Regulatory T Cells in GVHD Therapy

Graft versus host disease (GVHD) is a common complication and the leading cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Pharmacological immunosuppression used in GVHD prophylaxis and treatment lacks specificity and can increase the likelihood...

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Published inFrontiers in immunology Vol. 12; p. 697854
Main Authors Guo, Wen-wen, Su, Xiu-hua, Wang, Ming-yang, Han, Ming-zhe, Feng, Xiao-ming, Jiang, Er-lie
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 18.06.2021
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Summary:Graft versus host disease (GVHD) is a common complication and the leading cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Pharmacological immunosuppression used in GVHD prophylaxis and treatment lacks specificity and can increase the likelihood of infection and relapse. Regulatory T lymphocytes (Tregs) play a vital role in restraining excessive immune responses and inducing peripheral immune tolerance. In particular, clinical trials have demonstrated that Tregs can prevent and treat GVHD, without increasing the risk of relapse and infection. Hence, adoptive transfer of Tregs to control GVHD using their immunosuppressive properties represents a promising therapeutic approach. To optimally apply Tregs for control of GVHD, a thorough understanding of their biology is necessary. In this review, we describe the biological characteristics of Tregs, including how the stability of FOXP3 expression can be maintained. We will also discuss the mechanisms underlying Tregs-mediated modulation of GVHD and approaches to effectively increase Tregs’ numbers. Finally, we will examine the developing trends in the use of Tregs for clinical therapy.
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Reviewed by: Li Xuan, Southern Medical University, China; Paul G. Schlegel, University Children’s Hospital Würzburg, Germany; Mauro Di Ianni, University of Studies G. d’Annunzio Chieti and Pescara, Italy
This article was submitted to Alloimmunity and Transplantation, a section of the journal Frontiers in Immunology
These authors have contributed equally to this work
Edited by: Ping Zhang, Fred Hutchinson Cancer Research Center, United States
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.697854