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

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 signific...

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Veröffentlicht in:Biotechnology advances 2022-09, Vol.58, p.107917-107917, Article 107917
Hauptverfasser: Luginbuehl, Vera, Abraham, Eytan, Kovar, Karin, Flaaten, Richard, Müller, Antonia M S
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container_start_page 107917
container_title Biotechnology advances
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creator Luginbuehl, Vera
Abraham, Eytan
Kovar, Karin
Flaaten, Richard
Müller, Antonia M S
description 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. •CAR engineering represents a powerful technology for cancer immunotherapy.•Development of advanced CAR cell therapies requires interdisciplinary approaches.•Novel CAR-engineered cells could overcome some of the roadblocks in solid tumor treatment.•Technological and logistical solutions improve current manufacturing strategies.•Next generation CAR cel
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subjects Advanced manufacturing technologies
Antigens
Blood
Cancer
cancer immunotherapy
CAR discovery and development
CAR pharmacology
CAR-T cell therapy
Chimeric antigen receptor (CAR)
Clinical trials
Genetic Engineering
Humans
Immune system
Immunotherapy, Adoptive
Leukocytes
Leukocytes, Mononuclear
Lymphocytes
Macrophages
Natural killer cells
Neoplasms - therapy
Product development
Receptors, Chimeric Antigen - genetics
Stem cells
Supply chains
T-Lymphocytes
Tumor Microenvironment
Tumors
title Better by design: What to expect from novel CAR-engineered cell therapies?
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