Comparison of two lab-scale protocols for enhanced mRNA-based CAR-T cell generation and functionality.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
24 10 2023
Historique:
received: 21 03 2023
accepted: 17 10 2023
medline: 30 10 2023
pubmed: 25 10 2023
entrez: 24 10 2023
Statut: epublish

Résumé

Process development for transferring lab-scale research workflows to automated manufacturing procedures is critical for chimeric antigen receptor (CAR)-T cell therapies. Therefore, the key factor for cell viability, expansion, modification, and functionality is the optimal combination of medium and T cell activator as well as their regulatory compliance for later manufacturing under Good Manufacturing Practice (GMP). In this study, we compared two protocols for CAR-mRNA-modified T cell generation using our current lab-scale process, analyzed all mentioned parameters, and evaluated the protocols' potential for upscaling and process development of mRNA-based CAR-T cell therapies.

Identifiants

pubmed: 37875523
doi: 10.1038/s41598-023-45197-x
pii: 10.1038/s41598-023-45197-x
pmc: PMC10598065
doi:

Substances chimiques

Receptors, Chimeric Antigen 0
Cytokines 0
Receptors, Antigen, T-Cell 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

18160

Informations de copyright

© 2023. Springer Nature Limited.

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Auteurs

Nadine von Auw (N)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.

Robert Serfling (R)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.

Reni Kitte (R)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.

Nadja Hilger (N)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.

Chengkang Zhang (C)

Lonza, 9900 Medical Center Drive, Rockville, MD, 20850, USA.

Clara Gebhardt (C)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.

Anna Duenkel (A)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.

Paul Franz (P)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.

Ulrike Koehl (U)

Fraunhofer Cluster of Excellence Immune-Mediated Diseases CIMD, Leipzig, Germany.
Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.
Medical Faculty, Institute for Clinical Immunology, University of Leipzig, Johannisallee 30, 04103, Leipzig, Germany.

Stephan Fricke (S)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany.
Fraunhofer Cluster of Excellence Immune-Mediated Diseases CIMD, Leipzig, Germany.

U Sandy Tretbar (US)

Department for Cell and Gene Therapy Development, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Perlickstr. 1, 04103, Leipzig, Germany. sandy.tretbar@izi.fraunhofer.de.
Fraunhofer Cluster of Excellence Immune-Mediated Diseases CIMD, Leipzig, Germany. sandy.tretbar@izi.fraunhofer.de.

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Classifications MeSH