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嵌合抗原受体 T 细胞疗法(CAR-T)和同种异体干细胞移植在淋巴肿瘤中都有一席之地吗?

Do CAR-T and Allogeneic Stem Cell Transplant Both Have a Place in Lymphoid Neoplasms?

机构信息

Stem Cell Transplant and Cellular Therapies Unit, Great Metropolitan Hospital "Bianchi-Melacrino-Morelli", 89133 Reggio Calabria, Italy.

Stem Cell Transplant Program CIC 587, Great Metropolitan Hospital "Bianchi-Melacrino-Morelli", 89133 Reggio Calabria, Italy.

出版信息

Int J Mol Sci. 2023 Jan 5;24(2):1045. doi: 10.3390/ijms24021045.

DOI:10.3390/ijms24021045
PMID:36674573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9861434/
Abstract

Allogeneic stem cell transplantation (allo-SCT) represented the first immunotherapy to treat hematologic malignancies: it has been considered as a cure for the disease and never as an approach to extend the life of patients. The success of allo-SCT derives both from the ability to treat patients with intensive chemoradiotherapy and from the potent graft-versus-leukemia effects mediated by donor immunity. Although considerable progress has been made in the last years, significant barriers still remain in the form of disease relapse, graft-versus-host disease, infectious complications, and regimen-related toxicities. Moreover, the treatment of hematologic malignancies, particularly acute lymphoblastic leukemia and certain forms of lymphomas, has been revolutionized by the commercial introduction of genetically modified autologous T-lymphocyte therapy (CAR-T). Our review discusses current standards and the shifting paradigms in the indications for allo-SCT and the role of CAR-T cell therapy for lymphoid neoplasms.

摘要

异基因造血干细胞移植(allo-SCT)是治疗血液系统恶性肿瘤的第一种免疫疗法:它被认为是治愈疾病的方法,而不是延长患者生命的方法。allo-SCT 的成功既源于能够用强化化疗和放射治疗来治疗患者,也源于供者免疫介导的移植物抗白血病效应。尽管近年来取得了相当大的进展,但仍存在疾病复发、移植物抗宿主病、感染并发症和与方案相关的毒性等重大障碍。此外,由于基因修饰的自体 T 淋巴细胞治疗(CAR-T)的商业化引入,血液系统恶性肿瘤(尤其是急性淋巴细胞白血病和某些类型的淋巴瘤)的治疗发生了革命性变化。我们的综述讨论了 allo-SCT 适应证的当前标准和转变模式,以及 CAR-T 细胞治疗在淋巴肿瘤中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/cdaf061918a4/ijms-24-01045-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/7849e76d1e51/ijms-24-01045-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/bbe033e9ff8c/ijms-24-01045-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/d310063cb88a/ijms-24-01045-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/cdaf061918a4/ijms-24-01045-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/7849e76d1e51/ijms-24-01045-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/bbe033e9ff8c/ijms-24-01045-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/d310063cb88a/ijms-24-01045-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bda/9861434/cdaf061918a4/ijms-24-01045-g004.jpg

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Chimeric Antigen Receptor T-Cell Therapy: What We Expect Soon.
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Allogeneic Hematopoietic Cell Transplantation after Chimeric Antigen Receptor T Cell Therapy in Large B Cell Lymphoma.嵌合抗原受体 T 细胞治疗后异基因造血细胞移植治疗大 B 细胞淋巴瘤。
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