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单倍体相合移植后预防性输注供体来源的嵌合抗原受体T细胞:两例报告

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

作者信息

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

机构信息

Department of Hematology, Xinqiao Hospital, Army Medical University; State Key Laboratory of Trauma, Burns and Combined Injury, Chongqing.

Improvinglife Biotechnology Co. Ltd.

出版信息

Medicine (Baltimore). 2019 Jul;98(29):e16498. doi: 10.1097/MD.0000000000016498.

Abstract

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.

摘要

原理

复发是异基因造血干细胞移植(allo-HSCT)后死亡的主要原因。不幸的是,目前尚无有效的方法来预防allo-HSCT后的复发。嵌合抗原受体T(CAR-T)细胞因其强大的抗白血病活性,在难治性/复发性急性淋巴细胞白血病(ALL)的治疗中取得了良好的效果。然而,尚不清楚使用病毒系统构建的CAR-T细胞是否可作为预防性输注用于预防单倍体HSCT后的复发。

患者情况

两名高危ALL患者接受了单倍体HSCT。

诊断

两名患者均被诊断为高危ALL。

干预措施

患者在单倍体HSCT后第60天接受了使用病毒系统构建的供体来源CAR-T细胞的预防性输注。

结果

持续检测到CAR-T细胞,且未发生移植物抗宿主病。两名患者分别无病生存1年和6个月。

经验教训

单倍体HSCT后预防性输注供体来源的CAR-T细胞可能是安全的,且免疫抑制剂可能不会影响CAR-T细胞的增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9fb/6708817/cb415d85b078/medi-98-e16498-g001.jpg

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