Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia

ABSTRACTObjective The complex pathogenesis of relapsed and refractory (R/R) immune thrombocytopenia (ITP) contributes to the varied efficacy and tolerability of current treatment regimens. Rapamycin, an immunomodulatory agent, was originally used in the prevention of organ rejection after organ tran...

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Main Authors: Dan Wang, Kaniel Cassady, Zhongmin Zou, Xi Zhang, Yimei Feng
Format: Article
Language:English
Published: Taylor & Francis Group 2022-12-01
Series:Hematology
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/16078454.2022.2151230
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author Dan Wang
Kaniel Cassady
Zhongmin Zou
Xi Zhang
Yimei Feng
author_facet Dan Wang
Kaniel Cassady
Zhongmin Zou
Xi Zhang
Yimei Feng
author_sort Dan Wang
collection DOAJ
description ABSTRACTObjective The complex pathogenesis of relapsed and refractory (R/R) immune thrombocytopenia (ITP) contributes to the varied efficacy and tolerability of current treatment regimens. Rapamycin, an immunomodulatory agent, was originally used in the prevention of organ rejection after organ transplantation. Additional evidence now shows that rapamycin can successfully treat R/R ITP. Here, we summarize recent clinical progress on the role and potential mechanism of rapamycin in the treatment of ITP.Methods PubMed, Web of Science and CNKI database were searched to identify eligible studies, and the clinical data and preclinical studies on the use of mTOR inhibitors in ITP treatment were reviewed. The key results (efficacy and safety) of the most recent clinical reports were summarized.Results summarized Case series provide evidence of the effectiveness and tolerable safety profile of rapamycin in ITP, including primary and some secondary ITP. Mechanistic explorations indicate that rapamycin can regulate immune cell subsets (Th1, Th2, Th17, Treg, Breg, MDSC, etc.), modulate cytokine secretion (IL-6, IL-10, TGF-β, BAFF, etc.) and promote platelet autophagy.Conclusions Emerging clinical data and basic studies suggest that rapamycin, as a multifaceted regulator, could provide a new promising option for the therapy of ITP. Additional research is needed to identify those patients which may benefit the most, as well as therapeutic regimens with which rapamycin may be combined.
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spelling doaj.art-73654e23fb2c44029c14789a6cbf5ac12022-12-22T04:17:17ZengTaylor & Francis GroupHematology1607-84542022-12-012711282128910.1080/16078454.2022.2151230Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopeniaDan Wang0Kaniel Cassady1Zhongmin Zou2Xi Zhang3Yimei Feng4Medical Center of Hematology, The Xinqiao Hospital of Army Medical University, Chongqing, People’s Republic of ChinaRegeneron Pharmaceuticals, Tarrytown, NY, USADepartment of Chemical Defense Medicine, School of Military Preventive Medicine, Army Medical University, Chongqing, People’s Republic of ChinaMedical Center of Hematology, The Xinqiao Hospital of Army Medical University, Chongqing, People’s Republic of ChinaMedical Center of Hematology, The Xinqiao Hospital of Army Medical University, Chongqing, People’s Republic of ChinaABSTRACTObjective The complex pathogenesis of relapsed and refractory (R/R) immune thrombocytopenia (ITP) contributes to the varied efficacy and tolerability of current treatment regimens. Rapamycin, an immunomodulatory agent, was originally used in the prevention of organ rejection after organ transplantation. Additional evidence now shows that rapamycin can successfully treat R/R ITP. Here, we summarize recent clinical progress on the role and potential mechanism of rapamycin in the treatment of ITP.Methods PubMed, Web of Science and CNKI database were searched to identify eligible studies, and the clinical data and preclinical studies on the use of mTOR inhibitors in ITP treatment were reviewed. The key results (efficacy and safety) of the most recent clinical reports were summarized.Results summarized Case series provide evidence of the effectiveness and tolerable safety profile of rapamycin in ITP, including primary and some secondary ITP. Mechanistic explorations indicate that rapamycin can regulate immune cell subsets (Th1, Th2, Th17, Treg, Breg, MDSC, etc.), modulate cytokine secretion (IL-6, IL-10, TGF-β, BAFF, etc.) and promote platelet autophagy.Conclusions Emerging clinical data and basic studies suggest that rapamycin, as a multifaceted regulator, could provide a new promising option for the therapy of ITP. Additional research is needed to identify those patients which may benefit the most, as well as therapeutic regimens with which rapamycin may be combined.https://www.tandfonline.com/doi/10.1080/16078454.2022.2151230RapamycinITPimmune toleranceautophagyadverse effects
spellingShingle Dan Wang
Kaniel Cassady
Zhongmin Zou
Xi Zhang
Yimei Feng
Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia
Hematology
Rapamycin
ITP
immune tolerance
autophagy
adverse effects
title Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia
title_full Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia
title_fullStr Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia
title_full_unstemmed Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia
title_short Progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia
title_sort progress on the efficacy and potential mechanisms of rapamycin in the treatment of immune thrombocytopenia
topic Rapamycin
ITP
immune tolerance
autophagy
adverse effects
url https://www.tandfonline.com/doi/10.1080/16078454.2022.2151230
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