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Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report

RATIONALE: Relapse is the main cause of death after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Unfortunately, there are no efficient methods to prevent relapse after allo-HSCT. Chimeric antigen receptor T (CAR-T) cells have achieved favorable outcomes in the treatment of refract...

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Autores principales: Zhang, Cheng, Ma, Ying-Ying, Liu, Jun, Liu, Yao, Gao, Lei, Gao, Li, Kong, Pei-Yan, Xiong, Qing-Hui, Mei, Wei-Ling, Liu, Jia, Jiang, Peng-Fei, Ye, Xun, Zhong, Jiang F., Cao, Wei, Han, De-Ping, Zhang, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708817/
https://www.ncbi.nlm.nih.gov/pubmed/31335716
http://dx.doi.org/10.1097/MD.0000000000016498
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author Zhang, Cheng
Ma, Ying-Ying
Liu, Jun
Liu, Yao
Gao, Lei
Gao, Li
Kong, Pei-Yan
Xiong, Qing-Hui
Mei, Wei-Ling
Liu, Jia
Jiang, Peng-Fei
Ye, Xun
Zhong, Jiang F.
Cao, Wei
Han, De-Ping
Zhang, Xi
author_facet Zhang, Cheng
Ma, Ying-Ying
Liu, Jun
Liu, Yao
Gao, Lei
Gao, Li
Kong, Pei-Yan
Xiong, Qing-Hui
Mei, Wei-Ling
Liu, Jia
Jiang, Peng-Fei
Ye, Xun
Zhong, Jiang F.
Cao, Wei
Han, De-Ping
Zhang, Xi
author_sort Zhang, Cheng
collection PubMed
description RATIONALE: Relapse is the main cause of death after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Unfortunately, there are no efficient methods to prevent relapse after allo-HSCT. Chimeric antigen receptor T (CAR-T) cells have achieved favorable outcomes in the treatment of refractory/relapsed acute lymphoblastic leukemia (ALL) because of their strong anti-leukemia activity. However, it is unclear whether the CAR-T cells constructed using viral systems can be used as preventive infusions to prevent relapse after haploidentical HSCT. PATIENT CONCERNS: Two patients with ALL with high risk received haploidentical HSCT. DIAGNOSES: Two patients were diagnosed with ALL with high risk. INTERVENTIONS: Patients received preventive infusion of donor-derived CAR-T cells constructed using viral systems on day 60 after haploidentical HSCT. OUTCOMES: The CAR-T cells were continually detected, and no graft versus host disease developed. The two patients survived with disease-free for 1 year and 6 months, respectively. LESSONS: Preventive infusion of donor-derived CAR-T cells after haploidentical HSCT may be safe and that immunosuppressors may not affect the proliferation of CAR-T cells.
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spelling pubmed-67088172019-10-01 Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report Zhang, Cheng Ma, Ying-Ying Liu, Jun Liu, Yao Gao, Lei Gao, Li Kong, Pei-Yan Xiong, Qing-Hui Mei, Wei-Ling Liu, Jia Jiang, Peng-Fei Ye, Xun Zhong, Jiang F. Cao, Wei Han, De-Ping Zhang, Xi Medicine (Baltimore) Research Article RATIONALE: Relapse is the main cause of death after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Unfortunately, there are no efficient methods to prevent relapse after allo-HSCT. Chimeric antigen receptor T (CAR-T) cells have achieved favorable outcomes in the treatment of refractory/relapsed acute lymphoblastic leukemia (ALL) because of their strong anti-leukemia activity. However, it is unclear whether the CAR-T cells constructed using viral systems can be used as preventive infusions to prevent relapse after haploidentical HSCT. PATIENT CONCERNS: Two patients with ALL with high risk received haploidentical HSCT. DIAGNOSES: Two patients were diagnosed with ALL with high risk. INTERVENTIONS: Patients received preventive infusion of donor-derived CAR-T cells constructed using viral systems on day 60 after haploidentical HSCT. OUTCOMES: The CAR-T cells were continually detected, and no graft versus host disease developed. The two patients survived with disease-free for 1 year and 6 months, respectively. LESSONS: Preventive infusion of donor-derived CAR-T cells after haploidentical HSCT may be safe and that immunosuppressors may not affect the proliferation of CAR-T cells. Wolters Kluwer Health 2019-07-19 /pmc/articles/PMC6708817/ /pubmed/31335716 http://dx.doi.org/10.1097/MD.0000000000016498 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Research Article
Zhang, Cheng
Ma, Ying-Ying
Liu, Jun
Liu, Yao
Gao, Lei
Gao, Li
Kong, Pei-Yan
Xiong, Qing-Hui
Mei, Wei-Ling
Liu, Jia
Jiang, Peng-Fei
Ye, Xun
Zhong, Jiang F.
Cao, Wei
Han, De-Ping
Zhang, Xi
Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report
title Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report
title_full Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report
title_fullStr Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report
title_full_unstemmed Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report
title_short Preventive infusion of donor-derived CAR-T cells after haploidentical transplantation: Two cases report
title_sort preventive infusion of donor-derived car-t cells after haploidentical transplantation: two cases report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708817/
https://www.ncbi.nlm.nih.gov/pubmed/31335716
http://dx.doi.org/10.1097/MD.0000000000016498
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