Engineered therapeutic antibodies with mannose 6-phosphate analogues as a tool to degrade extracellular proteins.

M6Pn cancer immune diseases inflammatory diseases mannose 6-phosphate receptor targeted protein degradation therapeutic antibodies

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2024
Historique:
received: 05 08 2023
accepted: 14 02 2024
medline: 27 3 2024
pubmed: 27 3 2024
entrez: 27 3 2024
Statut: epublish

Résumé

Inducing the degradation of pathological soluble antigens could be the key to greatly enhancing the efficacy of therapeutic monoclonal antibodies (mAbs), extensively used in the treatment of autoimmune and inflammatory disorders or cancer. Lysosomal targeting has gained increasing interest in recent years due to its pharmaceutical applications far beyond the treatment of lysosomal diseases, as a way to address proteins to the lysosome for eventual degradation. Mannose 6-phosphonate derivatives (M6Pn), called AMFA, are unique glycovectors that can significantly enhance the cellular internalization of the proteins conjugated to AMFA

Identifiants

pubmed: 38533506
doi: 10.3389/fimmu.2024.1273280
pmc: PMC10964947
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1273280

Informations de copyright

Copyright © 2024 Daurat, Gauthier, El Cheikh, Ali, Morère, Bettache, Gary-Bobo, Morère, Garcia, Maynadier and Basile.

Déclaration de conflit d'intérêts

Authors MD, CG, KEC, EM, MG, MM, and IB were employed by the company NanoMedSyn. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Morgane Daurat (M)

NanoMedSyn, Montpellier, France.

Corentin Gauthier (C)

NanoMedSyn, Montpellier, France.
Institut des Biomolécules Max Mousseron (IBMM), University of Montpellier, CNRS, ENSCM, Montpellier, France.

Khaled El Cheikh (K)

NanoMedSyn, Montpellier, France.

Lamiaa M A Ali (LMA)

Institut des Biomolécules Max Mousseron (IBMM), University of Montpellier, CNRS, ENSCM, Montpellier, France.
Department of Biochemistry Medical Research Institute, University of Alexandria, Alexandria, Egypt.

Elodie Morère (E)

NanoMedSyn, Montpellier, France.
Institut des Biomolécules Max Mousseron (IBMM), University of Montpellier, CNRS, ENSCM, Montpellier, France.

Nadir Bettache (N)

Institut des Biomolécules Max Mousseron (IBMM), University of Montpellier, CNRS, ENSCM, Montpellier, France.

Magali Gary-Bobo (M)

Institut des Biomolécules Max Mousseron (IBMM), University of Montpellier, CNRS, ENSCM, Montpellier, France.

Alain Morère (A)

Institut des Biomolécules Max Mousseron (IBMM), University of Montpellier, CNRS, ENSCM, Montpellier, France.

Marcel Garcia (M)

NanoMedSyn, Montpellier, France.

Marie Maynadier (M)

NanoMedSyn, Montpellier, France.

Ilaria Basile (I)

NanoMedSyn, Montpellier, France.

Classifications MeSH