Suppr超能文献

异基因造血干细胞移植后复发的急性髓系白血病的细胞治疗

Cell-Based Treatment in Acute Myeloid Leukemia Relapsed after Allogeneic Stem Cell Transplantation.

作者信息

Canichella Martina, de Fabritiis Paolo

机构信息

Hematology Unit, St. Eugenio Hospital, ASL Roma2, 00144 Rome, Italy.

Department of Biomedicine and Prevention, Tor Vergata University, 00133 Rome, Italy.

出版信息

Biomedicines. 2024 Aug 1;12(8):1721. doi: 10.3390/biomedicines12081721.

Abstract

Allogeneic stem cell transplant (ASCT) remains the only treatment option for patients with high-risk acute myeloid leukemia (AML). Recurrence of leukemic cells after ASCT represents a dramatic event associated with a dismal outcome, with a 2-year survival rate of around 20%. Adoptive cell therapy (ACT) is a form of cell-based strategy that has emerged as an effective therapy to treat and prevent post-ASCT recurrence. Lymphocytes are the principal cells used in this therapy and can be derived from a hematopoietic stem cell donor, the patient themselves, or healthy donors, after being engineered to express the chimeric antigen receptor (CAR-T and UniCAR-T). In this review, we discuss recent advances in the established strategy of donor lymphocyte infusion (DLI) and the progress and challenges of CAR-T cells.

摘要

异基因干细胞移植(ASCT)仍然是高危急性髓系白血病(AML)患者的唯一治疗选择。ASCT后白血病细胞复发是一个与预后不良相关的重大事件,2年生存率约为20%。过继性细胞疗法(ACT)是一种基于细胞的策略,已成为治疗和预防ASCT后复发的有效疗法。淋巴细胞是该疗法中使用的主要细胞,可以来自造血干细胞供体、患者自身或健康供体,经过工程改造以表达嵌合抗原受体(CAR-T和UniCAR-T)。在本综述中,我们讨论了已确立的供体淋巴细胞输注(DLI)策略的最新进展以及CAR-T细胞的进展和挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0923/11351713/ee48cb742501/biomedicines-12-01721-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验