Immunogenicity of CRISPR therapeutics-Critical considerations for clinical translation.

CRISPR-Cas Cas9 clinical translation clinical trials gene therapy genome editing immunogenicity

Journal

Frontiers in bioengineering and biotechnology
ISSN: 2296-4185
Titre abrégé: Front Bioeng Biotechnol
Pays: Switzerland
ID NLM: 101632513

Informations de publication

Date de publication:
2023
Historique:
received: 05 01 2023
accepted: 06 02 2023
entrez: 6 3 2023
pubmed: 7 3 2023
medline: 7 3 2023
Statut: epublish

Résumé

CRISPR offers new hope for many patients and promises to transform the way we think of future therapies. Ensuring safety of CRISPR therapeutics is a top priority for clinical translation and specific recommendations have been recently released by the FDA. Rapid progress in the preclinical and clinical development of CRISPR therapeutics leverages years of experience with gene therapy successes and failures. Adverse events due to immunogenicity have been a major setback that has impacted the field of gene therapy. As several

Identifiants

pubmed: 36873375
doi: 10.3389/fbioe.2023.1138596
pii: 1138596
pmc: PMC9978118
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1138596

Informations de copyright

Copyright © 2023 Ewaisha and Anderson.

Déclaration de conflit d'intérêts

RE and KSA are noted as inventors on a patent regarding Cas9 immunity.

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Auteurs

Radwa Ewaisha (R)

Department of Microbiology and Immunology, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
Department of Microbiology and Immunology, School of Pharmacy, Newgiza University, Newgiza, Egypt.

Karen S Anderson (KS)

Center for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ, United States.

Classifications MeSH