The Spectrum of CAR Cellular Effectors: Modes of Action in Anti-Tumor Immunity.

adoptive cell therapy chemokines chimeric antigen receptor cytokines dendritic cells gamma-delta T cells killing mechanism kinetics macrophages mode of action natural killer cells persistence

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
22 Jul 2024
Historique:
received: 16 06 2024
revised: 13 07 2024
accepted: 17 07 2024
medline: 27 7 2024
pubmed: 27 7 2024
entrez: 27 7 2024
Statut: epublish

Résumé

Chimeric antigen receptor-T cells have spearheaded the field of adoptive cell therapy and have shown remarkable results in treating hematological neoplasia. Because of the different biology of solid tumors compared to hematological tumors, response rates of CAR-T cells could not be transferred to solid entities yet. CAR engineering has added co-stimulatory domains, transgenic cytokines and switch receptors to improve performance and persistence in a hostile tumor microenvironment, but because of the inherent cell type limitations of CAR-T cells, including HLA incompatibility, toxicities (cytokine release syndrome, neurotoxicity) and high costs due to the logistically challenging preparation process for autologous cells, the use of alternative immune cells is gaining traction. NK cells and γδ T cells that do not need HLA compatibility or macrophages and dendritic cells with additional properties such as phagocytosis or antigen presentation are increasingly seen as cellular vehicles with potential for application. As these cells possess distinct properties, clinicians and researchers need a thorough understanding of their peculiarities and commonalities. This review will compare these different cell types and their specific modes of action seen upon CAR activation.

Identifiants

pubmed: 39061247
pii: cancers16142608
doi: 10.3390/cancers16142608
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Auteurs

Ngoc Thien Thu Nguyen (NTT)

Division of Clinical Pharmacology, Department of Medicine IV, LMU University Hospital, LMU Munich, 80336 Munich, Germany.
German Cancer Consortium (DKTK), Partner Site Munich, a Partnership between the DKFZ Heidelberg and the University Hospital of the LMU, 80336 Munich, Germany.

Rasmus Müller (R)

Division of Clinical Pharmacology, Department of Medicine IV, LMU University Hospital, LMU Munich, 80336 Munich, Germany.

Daria Briukhovetska (D)

Division of Clinical Pharmacology, Department of Medicine IV, LMU University Hospital, LMU Munich, 80336 Munich, Germany.

Justus Weber (J)

Department of Medicine II, Chair in Cellular Immunotherapy, University Hospital Würzburg, 97080 Würzburg, Germany.

Judith Feucht (J)

Cluster of Excellence iFIT "Image-Guided and Functionally Instructed Tumor Therapies", University of Tübingen, 72076 Tuebingen, Germany.
Department of Hematology and Oncology, University Children's Hospital Tuebingen, University of Tübingen, 72076 Tuebingen, Germany.

Annette Künkele (A)

Department of Pediatric Oncology/Hematology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, 13353 Berlin, Germany.
German Cancer Consortium (DKTK), Partner Site Berlin, 10117 Berlin, Germany.

Michael Hudecek (M)

Department of Medicine II, Chair in Cellular Immunotherapy, University Hospital Würzburg, 97080 Würzburg, Germany.
Fraunhofer Institute for Cell Therapy and Immunology, Cellular Immunotherapy Branch Site Würzburg, 97080 Würzburg, Germany.

Sebastian Kobold (S)

Division of Clinical Pharmacology, Department of Medicine IV, LMU University Hospital, LMU Munich, 80336 Munich, Germany.
German Cancer Consortium (DKTK), Partner Site Munich, a Partnership between the DKFZ Heidelberg and the University Hospital of the LMU, 80336 Munich, Germany.
Einheit für Klinische Pharmakologie (EKLiP), Helmholtz Zentrum München-German Research Center for Environmental Health Neuherberg, 85764 Oberschleißheim, Germany.

Classifications MeSH