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靶向CD22治疗B细胞恶性肿瘤。

Targeting CD22 for the Treatment of B-Cell Malignancies.

作者信息

Shah Nikesh N, Sokol Lubomir

机构信息

Department of Internal Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.

Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

出版信息

Immunotargets Ther. 2021 Jul 6;10:225-236. doi: 10.2147/ITT.S288546. eCollection 2021.


DOI:10.2147/ITT.S288546
PMID:34262884
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8275043/
Abstract

Immunotherapeutic agents play an increasingly important role in the treatment of B-cell malignancies. CD19 and CD20 are common targets for lymphoid malignancies, though patients who relapse have few therapeutic options remaining. CD22 is a cell surface sialoglycoprotein uniquely present on B-cells and regulates B-cell function and proliferation. Thus, it is an appealing therapeutic target for autoimmune disorders and B-cell malignancies. A variety of therapies targeting CD22 have been developed, including monoclonal antibodies, antibody-drug conjugates, radioimmunoconjugates, chimeric antigen receptor T cells, and bispecific antibodies. Here, we review the biology of CD22 and key therapies targeting CD22 in lymphoid malignancies.

摘要

免疫治疗药物在B细胞恶性肿瘤的治疗中发挥着越来越重要的作用。CD19和CD20是淋巴恶性肿瘤的常见靶点,不过复发的患者几乎没有剩余的治疗选择。CD22是一种独特地存在于B细胞上的细胞表面唾液酸糖蛋白,可调节B细胞功能和增殖。因此,它是自身免疫性疾病和B细胞恶性肿瘤的一个有吸引力的治疗靶点。已经开发了多种针对CD22的疗法,包括单克隆抗体、抗体药物偶联物、放射免疫偶联物、嵌合抗原受体T细胞和双特异性抗体。在此,我们综述CD22的生物学特性以及在淋巴恶性肿瘤中针对CD22的关键疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8184/8275043/687358407f73/ITT-10-225-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8184/8275043/687358407f73/ITT-10-225-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8184/8275043/687358407f73/ITT-10-225-g0001.jpg

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[9]
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[10]
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本文引用的文献

[1]
Th-Labeled Anti-CD22 Antibody (BAY 1862864) in Relapsed/Refractory CD22-Positive Non-Hodgkin Lymphoma: A First-in-Human, Phase I Study.

Cancer Biother Radiopharm. 2021-10

[2]
Trispecific CD19-CD20-CD22-targeting duoCAR-T cells eliminate antigen-heterogeneous B cell tumors in preclinical models.

Sci Transl Med. 2021-3-24

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Adoptive Immunotherapy beyond CAR T-Cells.

Cancers (Basel). 2021-2-11

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J Clin Oncol. 2020-6-10

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J Hematol Oncol. 2020-4-3

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[8]
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[9]
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[10]
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Lancet Oncol. 2018-1-16

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