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Better by design: What to expect from novel CAR-engineered cell therapies?

作者信息

Luginbuehl Vera, Abraham Eytan, Kovar Karin, Flaaten Richard, Müller Antonia M S

机构信息

Novartis Oncology, Cell & Gene Therapy, Novartis Pharma Schweiz AG, Rotkreuz, Switzerland.

Personalized Medicine Lonza Pharma&Biotech, Lonza Ltd., Walkersville, MD, USA.

出版信息

Biotechnol Adv. 2022 Sep;58:107917. doi: 10.1016/j.biotechadv.2022.107917. Epub 2022 Feb 9.


DOI:10.1016/j.biotechadv.2022.107917
PMID:35149146
Abstract

Chimeric antigen receptor (CAR) technology, and CAR-T cells in particular, have emerged as a new and powerful tool in cancer immunotherapy since demonstrating efficacy against several hematological malignancies. However, despite encouraging clinical results of CAR-T cell therapy products, a significant proportion of patients do not achieve satisfactory responses, or relapse. In addition, CAR-T cell applications to solid tumors is still limited due to the tumor microenvironment and lack of specifically targetable tumor antigens. All current products on the market, as well as most investigational CAR-T cell therapies, are autologous, using the patient's own peripheral blood mononuclear cells as starting material to manufacture a patient-specific batch. Alternative cell sources are, therefore, under investigation (e.g. allogeneic cells from an at least partially human leukocyte antigen (HLA)-matched healthy donor, universal "third-party" cells from a non-HLA-matched donor, cord blood-derived cells, immortalized cell lines or cells differentiated from induced pluripotent stem cells). However, genetic modifications of CAR-engineered cells, bioprocesses used to expand cells, and improved supply chains are still complex and costly. To overcome drawbacks associated with CAR-T technologies, novel CAR designs have been used to genetically engineer cells derived from alpha beta (αβ) T cells, other immune cells such as natural killer (NK) cells, gamma delta (γδ) T cells, macrophages or dendritic cells. This review endeavours to trigger ideas on the next generation of CAR-engineered cell therapies beyond CAR-T cells and, thus, will enable effective, safe and affordable therapies for clinical management of cancer. To achieve this, we present a multidisciplinary overview, addressing a wide range of critical aspects: CAR design, development and manufacturing technologies, pharmacological concepts and clinical applications of CAR-engineered cell therapies. Each of these fields employs a large number of ground-breaking scientific advances, where coordinated and complex process and product development occur at their interfaces.

摘要

相似文献

[1]
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Biotechnol Adv. 2022-9

[2]
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[3]
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[4]
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[7]
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[2]
CAR-T therapy for endocrine neoplasms: novel targets and combination of therapies.

Front Endocrinol (Lausanne). 2025-2-11

[3]
Non-viral approaches in CAR-NK cell engineering: connecting natural killer cell biology and gene delivery.

J Nanobiotechnology. 2024-9-10

[4]
CAR products from novel sources: a new avenue for the breakthrough in cancer immunotherapy.

Front Immunol. 2024

[5]
Advanced Strategies of CAR-T Cell Therapy in Solid Tumors and Hematological Malignancies.

Recent Pat Anticancer Drug Discov. 2024

[6]
The application of HER2 and CD47 CAR-macrophage in ovarian cancer.

J Transl Med. 2023-9-22

[7]
Clinical application and prospect of immune checkpoint inhibitors for CAR-NK cell in tumor immunotherapy.

Front Immunol. 2022

[8]
Decoding Roles of Exosomal lncRNAs in Tumor-Immune Regulation and Therapeutic Potential.

Cancers (Basel). 2022-12-31

[9]
Natural killer cell homing and trafficking in tissues and tumors: from biology to application.

Signal Transduct Target Ther. 2022-6-29

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