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利用 CAR-T 细胞疗法治疗实体瘤的新方法。

Emerging Approaches for Solid Tumor Treatment Using CAR-T Cell Therapy.

机构信息

Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Daejeon 34141, Korea.

College of Pharmacy, Chungnam National University, Yuseong-gu, Daejeon 34134, Korea.

出版信息

Int J Mol Sci. 2021 Nov 9;22(22):12126. doi: 10.3390/ijms222212126.


DOI:10.3390/ijms222212126
PMID:34830003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8621681/
Abstract

Cancer immunotherapy is becoming more important in the clinical setting, especially for cancers resistant to conventional chemotherapy, including targeted therapy. Chimeric antigen receptor (CAR)-T cell therapy, which uses patient's autologous T cells, combined with engineered T cell receptors, has shown remarkable results, with five US Food and Drug Administration (FDA) approvals to date. CAR-T cells have been very effective in hematologic malignancies, such as diffuse large B cell lymphoma (DLBCL), B cell acute lymphoblastic leukemia (B-ALL), and multiple myeloma (MM); however, its effectiveness in treating solid tumors has not been evaluated clearly. Therefore, many studies and clinical investigations are emerging to improve the CAR-T cell efficacy in solid tumors. The novel therapeutic approaches include modifying CARs in multiple ways or developing a combination therapy with immune checkpoint inhibitors and chemotherapies. In this review, we focus on the challenges and recent advancements in CAR-T cell therapy for solid tumors.

摘要

癌症免疫疗法在临床环境中变得越来越重要,特别是对于对传统化疗(包括靶向治疗)耐药的癌症。嵌合抗原受体 (CAR)-T 细胞疗法利用患者自身的 T 细胞,并结合工程化的 T 细胞受体,已取得显著成果,迄今为止已有 5 项美国食品和药物管理局 (FDA) 批准。CAR-T 细胞在血液恶性肿瘤中非常有效,例如弥漫性大 B 细胞淋巴瘤 (DLBCL)、B 细胞急性淋巴细胞白血病 (B-ALL) 和多发性骨髓瘤 (MM);然而,其在治疗实体瘤方面的疗效尚未得到明确评估。因此,许多研究和临床调查正在涌现,以提高 CAR-T 细胞在实体瘤中的疗效。新的治疗方法包括以多种方式修饰 CAR 或与免疫检查点抑制剂和化疗联合治疗。在这篇综述中,我们重点介绍了 CAR-T 细胞治疗实体瘤所面临的挑战和最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f681/8621681/c1d8420fdf49/ijms-22-12126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f681/8621681/a8e3e324ff22/ijms-22-12126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f681/8621681/c1d8420fdf49/ijms-22-12126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f681/8621681/a8e3e324ff22/ijms-22-12126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f681/8621681/c1d8420fdf49/ijms-22-12126-g002.jpg

相似文献

[1]
Emerging Approaches for Solid Tumor Treatment Using CAR-T Cell Therapy.

Int J Mol Sci. 2021-11-9

[2]
Risks and Benefits of Chimeric Antigen Receptor T-Cell (CAR-T) Therapy in Cancer: A Systematic Review and Meta-Analysis.

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[3]
Driving CARs on the Highway to Solid Cancer: Some Considerations on the Adoptive Therapy with CAR T Cells.

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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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[3]
Significant Advancements and Evolutions in Chimeric Antigen Receptor Design.

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[4]
Novel therapeutic agents in clinical trials: emerging approaches in cancer therapy.

Discov Oncol. 2024-8-11

[5]
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Mol Ther Oncol. 2024-6-24

[6]
CRISPR, CAR-T, and NK: Current applications and future perspectives.

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[7]
Recent advances and future perspectives of CAR-T cell therapy in head and neck cancer.

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[8]
The future of cancer immunotherapy: DNA vaccines leading the way.

Med Oncol. 2023-6-9

[9]
CAR-NKT cell therapy: a new promising paradigm of cancer immunotherapy.

Cancer Cell Int. 2023-5-8

[10]
Tuning CARs: recent advances in modulating chimeric antigen receptor (CAR) T cell activity for improved safety, efficacy, and flexibility.

J Transl Med. 2023-3-15

本文引用的文献

[1]
Gene-Edited Interleukin CAR-T Cells Therapy in the Treatment of Malignancies: Present and Future.

Front Immunol. 2021

[2]
CAR T-Cells for CNS Lymphoma: Driving into New Terrain?

Cancers (Basel). 2021-5-20

[3]
CRISPR/Cas9 mediated deletion of the adenosine A2A receptor enhances CAR T cell efficacy.

Nat Commun. 2021-5-28

[4]
Phase I clinical trial of EGFR-specific CAR-T cells generated by the piggyBac transposon system in advanced relapsed/refractory non-small cell lung cancer patients.

J Cancer Res Clin Oncol. 2021-12

[5]
Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma.

J Clin Oncol. 2021-8-20

[6]
Antigen-independent activation enhances the efficacy of 4-1BB-costimulated CD22 CAR T cells.

Nat Med. 2021-5

[7]
CAR-T cell therapy: current limitations and potential strategies.

Blood Cancer J. 2021-4-6

[8]
Enhancing CAR-T cell efficacy in solid tumors by targeting the tumor microenvironment.

Cell Mol Immunol. 2021-5

[9]
Role of the Orphan Nuclear Receptor NR4A Family in T-Cell Biology.

Front Endocrinol (Lausanne). 2020

[10]
Mesenchymal stromal cell delivery of oncolytic immunotherapy improves CAR-T cell antitumor activity.

Mol Ther. 2021-5-5

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