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自然选择 CD7 导向嵌合抗原受体 T 细胞桥接异基因造血干细胞移植治疗难治性急性髓系白血病:一例病例报告并复习。

Naturally selected CD7-directed CAR-T bridging allo-HSCT in refractory acute myeloid leukemia: a case report and review.

机构信息

Department of Hematology, The Second Hospital of Hebei Medical University, Hebei Key Laboratory of Hematology, Shijiazhuang, Hebei, China.

Hebei Senlang Biotechnology Co, Shijiazhuang, China.

出版信息

Front Immunol. 2024 Oct 14;15:1461908. doi: 10.3389/fimmu.2024.1461908. eCollection 2024.

DOI:10.3389/fimmu.2024.1461908
PMID:39469704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11513260/
Abstract

Relapsed/refractory acute myeloid leukemia (R/R-AML) has a poor prognosis. CD7 is expressed in leukemic cells in 30% of patients with AML but not in normal myeloid cells. Therefore, it can be a potential target for immunotherapy in patients with R/R-AML. Naturally selected CD7-directed chimeric antigen receptor T cells (CAR-T) have promising effects against AML based on xenotransplantation models. We report a R/R-AML case that achieved complete remission with incomplete hematologic recovery with naturally selected CD7 CAR-T therapy. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) as consolidation early after CAR T therapy, the patient experienced 12 months of disease-free survival to date. Our results confirmed that allogeneic hematopoietic stem cell transplantation after naturally selected CD7 CAR-T therapy can be a potential treatment for patients with CD7-positive R/R-AML.

摘要

复发/难治性急性髓系白血病(R/R-AML)预后不良。CD7 在 30%的 AML 患者的白血病细胞中表达,但不在正常髓系细胞中表达。因此,它可能成为 R/R-AML 患者免疫治疗的潜在靶点。基于异种移植模型,自然选择的 CD7 导向嵌合抗原受体 T 细胞(CAR-T)对 AML 具有有前景的疗效。我们报告了一例 R/R-AML 病例,该病例在接受自然选择的 CD7 CAR-T 治疗后实现了不完全血液学恢复的完全缓解。在 CAR-T 治疗后早期进行异基因造血干细胞移植(allo-HSCT)作为巩固治疗,患者至今已无疾病生存 12 个月。我们的结果证实,自然选择的 CD7 CAR-T 治疗后进行异基因造血干细胞移植可能是治疗 CD7 阳性 R/R-AML 患者的一种潜在方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2f/11513260/3079ed8dfa66/fimmu-15-1461908-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2f/11513260/be7efdf73077/fimmu-15-1461908-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2f/11513260/3079ed8dfa66/fimmu-15-1461908-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2f/11513260/be7efdf73077/fimmu-15-1461908-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2f/11513260/3079ed8dfa66/fimmu-15-1461908-g002.jpg

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本文引用的文献

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J Transl Med. 2022 Dec 14;20(1):600. doi: 10.1186/s12967-022-03797-7.
2
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Exp Hematol Oncol. 2022 Sep 29;11(1):67. doi: 10.1186/s40164-022-00318-6.
3
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Cell Res. 2022 Nov;32(11):995-1007. doi: 10.1038/s41422-022-00721-y. Epub 2022 Sep 23.
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