HLA-DR expression in melanoma: from misleading therapeutic target to potential immunotherapy biomarker.

BRAF HLA-DR MHC-II NRAS anti-PD1 immunotherapy melanoma

Journal

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

Informations de publication

Date de publication:
2023
Historique:
received: 30 08 2023
accepted: 26 12 2023
medline: 1 2 2024
pubmed: 1 2 2024
entrez: 1 2 2024
Statut: epublish

Résumé

Since the advent of anti-PD1 immune checkpoint inhibitor (ICI) immunotherapy, cutaneous melanoma has undergone a true revolution with prolonged survival, as available 5-year updates for progression-free survival and overall survival demonstrate a durable clinical benefit for melanoma patients receiving ICI. However, almost half of patients fail to respond to treatment, or relapse sooner or later after the initial response to therapy. Little is known about the reasons for these failures. The identification of biomarkers seems necessary to better understand this resistance. Among these biomarkers, HLA-DR, a component of MHC II and abnormally expressed in certain tumor types including melanoma for unknown reasons, seems to be an interesting marker. The aim of this review, prepared by an interdisciplinary group of experts, is to take stock of the current literature on the potential interest of HLA-DR expression in melanoma as a predictive biomarker of ICI outcome.

Identifiants

pubmed: 38299143
doi: 10.3389/fimmu.2023.1285895
pmc: PMC10827890
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1285895

Informations de copyright

Copyright © 2024 Amrane, Le Meur, Besse, Hemon, Le Noac’h, Pradier, Berthou, Abgral and Uguen.

Déclaration de conflit d'intérêts

The 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. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Karim Amrane (K)

Department of Oncology, Regional Hospital of Morlaix, Morlaix, France.
Inserm, Unité mixte de recherche (UMR1227), Lymphocytes B et Autoimmunité, Univ Brest, Inserm, LabEx Immunotherapy-Graft-Oncology (IGO), Brest, France.

Coline Le Meur (C)

Department of Radiotherapy, University Hospital of Brest, Brest, France.

Benjamin Besse (B)

Department of Cancer Medicine, Gustave Roussy Cancer Centre, Villejuif, France.
Faculty of Medicine, University Paris-Saclay, Le Kremlin Bicêtre, France.

Patrice Hemon (P)

Inserm, Unité mixte de recherche (UMR1227), Lymphocytes B et Autoimmunité, Univ Brest, Inserm, LabEx Immunotherapy-Graft-Oncology (IGO), Brest, France.

Pierre Le Noac'h (P)

Inserm, Unité mixte de recherche (UMR1227), Lymphocytes B et Autoimmunité, Univ Brest, Inserm, LabEx Immunotherapy-Graft-Oncology (IGO), Brest, France.
Department of Pathology, University Hospital of Brest, Brest, France.

Olivier Pradier (O)

Department of Radiotherapy, University Hospital of Brest, Brest, France.

Christian Berthou (C)

Inserm, Unité mixte de recherche (UMR1227), Lymphocytes B et Autoimmunité, Univ Brest, Inserm, LabEx Immunotherapy-Graft-Oncology (IGO), Brest, France.
Department of Hematology, University Hospital of Brest, Brest, France.

Ronan Abgral (R)

Department of Nuclear Medicine, University Hospital of Brest, Brest, France.
UMR Inserm 1304 Groupe d'Étude de la Thrombose de Bretagne Occidentale (GETBO), IFR 148, University of Western Brittany, Brest, France.

Arnaud Uguen (A)

Inserm, Unité mixte de recherche (UMR1227), Lymphocytes B et Autoimmunité, Univ Brest, Inserm, LabEx Immunotherapy-Graft-Oncology (IGO), Brest, France.
Department of Pathology, University Hospital of Brest, Brest, France.

Classifications MeSH