Emerging approaches to induce immune tolerance to therapeutic proteins.

antidrug antibodies immune tolerance immunogenicity protein therapeutics

Journal

Trends in pharmacological sciences
ISSN: 1873-3735
Titre abrégé: Trends Pharmacol Sci
Pays: England
ID NLM: 7906158

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 25 09 2023
revised: 04 10 2023
accepted: 08 10 2023
medline: 20 11 2023
pubmed: 31 10 2023
entrez: 30 10 2023
Statut: ppublish

Résumé

Immunogenicity affects the safety and efficacy of therapeutic proteins. This review is focused on approaches for inducing immunological tolerance to circumvent the immunogenicity of therapeutic proteins in the clinic. The few immune tolerance strategies that are used in the clinic tend to be inefficient and expensive and typically involve global immunosuppression, putting patients at risk of infections. The hallmark of a desirable immune tolerance regimen is the specific alleviation of immune responses to the therapeutic protein. In the past decade, proof-of-principle studies have demonstrated that emerging technologies, including nanoparticle-based delivery of immunomodulators, cellular targeting and depletion, cellular engineering, gene therapy, and gene editing, can be leveraged to promote tolerance to therapeutic proteins. We discuss the potential of these novel approaches and the barriers that need to be overcome for translation into the clinic.

Identifiants

pubmed: 37903706
pii: S0165-6147(23)00235-3
doi: 10.1016/j.tips.2023.10.002
pii:
doi:

Substances chimiques

Immunologic Factors 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1028-1042

Informations de copyright

Copyright © 2023. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of interests Our contributions are an informal communication and represent our own best judgment. These comments do not bind or obligate the FDA. The authors have no interests to declare.

Auteurs

Justine C Noel (JC)

Division of Hemostasis, Office of Plasma Protein Therapeutics, Center for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.

Daniel Lagassé (D)

Division of Hemostasis, Office of Plasma Protein Therapeutics, Center for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.

Basil Golding (B)

Division of Plasma Derivatives, Office of Plasma Protein Therapeutics, Center for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA.

Zuben E Sauna (ZE)

Division of Hemostasis, Office of Plasma Protein Therapeutics, Center for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA. Electronic address: zuben.sauna@fda.hhs.gov.

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Classifications MeSH