The anti-B7-H3 blocking antibody MJ18 does not recognize B7-H3 in murine tumor models.


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
17 Nov 2023
Historique:
pubmed: 28 11 2023
medline: 28 11 2023
entrez: 28 11 2023
Statut: epublish

Résumé

The immune checkpoint molecule B7-H3 is regarded as one of the most promising therapeutic targets for the treatment of human cancers. B7-H3 is highly expressed in many cancers and its expression has been associated to impaired antitumor immunity and poor patient prognosis. In immunocompetent mouse tumor models, genetic deletion of B7-H3 in tumor cells enhances antitumor immune response leading to tumor shrinkage. The underlying mechanisms of B7-H3 inhibitory function remain largely uncharacterized and the identity of potential cognate(s) receptor(s) of B7-H3 is still to be defined. To better understand B7-H3 function

Identifiants

pubmed: 38014341
doi: 10.1101/2023.11.15.567261
pmc: PMC10680724
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : P30 CA015083
Pays : United States

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Auteurs

Talah Nammor (T)

Department of Urology, Mayo Clinic, Rochester, MN, USA.

Jenna Frizzell (J)

Department of Urology, Mayo Clinic, Rochester, MN, USA.

Roxane R Lavoie (RR)

Department of Urology, Mayo Clinic, Rochester, MN, USA.

Fabrice Lucien (F)

Department of Urology, Mayo Clinic, Rochester, MN, USA.
Department of Immunology, Mayo Clinic, Rochester, MN, USA.

Classifications MeSH