← 返回

受者来源异基因 CAR-T 细胞治疗后儿科患者因特发性肺炎综合征导致的呼吸衰竭

英文原题:Respiratory Failure Due to Idiopathic Pneumonia Syndrome in a Pediatric Patient After Recipient-derived Allogeneic Chimeric Antigen Receptor T-Cell Therapy.

查看英文原题

Respiratory Failure Due to Idiopathic Pneumonia Syndrome in a Pediatric Patient After Recipient-derived Allogeneic Chimeric Antigen Receptor T-Cell Therapy.

PubMed 2023/06/07(内容时间) J Pediatr Hematol Oncol Q3 · IF 0.9(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

特发性肺炎综合征(IPS)是造血细胞移植后一种危及生命的并发症,但在嵌合抗原受体(CAR)T细胞治疗后尚未得到明确描述。我们描述了一名儿童,因造血细胞移植后复发性急性淋巴细胞白血病接受tisagenlecleucel治疗后发生IPS,经皮质类固醇和依那西普治疗后获得显著改善。我们讨论了细胞因子信号在IPS中的意义以及异基因CAR-T 细胞的免疫学考量。我们预计,随着异基因CAR-T 细胞在更多样化的环境中、使用更多错配供者,IPS和其他异基因现象的发生率将被更频繁地观察到。

展开英文摘要原文

Idiopathic pneumonia syndrome (IPS) is a life-threatening complication of hematopoietic cell transplantation, but it is not clearly described following chimeric antigen receptor (CAR) T-cell therapy.

We describe a child who developed IPS after receiving tisagenlecleucel for post-hematopoietic cell transplantation relapsed acute lymphoblastic leukemia and had a remarkable improvement after treatment with corticosteroids and etanercept.

We discuss the implications of cytokine signaling in IPS and immunologic considerations of allogeneic CAR T cells.

We anticipate that the incidence of IPS and other allogeneic phenomena will be observed more often as allogeneic CAR T cells are employed in more varied settings with more mismatched donors.

论文信息

作者
Zipper R、Loeb DM、Lee MA、Oliver-Krasinski J、Liszewski MC、Fraint E
第一作者单位
Departments of Pediatrics.
通讯作者单位
Division of Pediatric Hematology, Oncology, and Cellular Therapy, Children's Hospital at Montefiore.
期刊
Journal of pediatric hematology/oncology2023 Aug 1
原文标识
PubMed 37314946 · DOI 10.1097/MPH.0000000000002693