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
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
1273280Informations 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.