[Bispecific antibodies in multiple myeloma].
Myélome multiple et anticorps bispécifiques.
ADP-ribosyl Cyclase 1
/ immunology
Antibodies, Bispecific
/ immunology
Antigens, Neoplasm
/ immunology
Drug Resistance, Neoplasm
/ immunology
Humans
Immunotherapy
/ methods
Multiple Myeloma
/ immunology
Receptors, Fc
/ immunology
Receptors, G-Protein-Coupled
/ immunology
Signaling Lymphocytic Activation Molecule Family
/ immunology
T-Lymphocytes
/ immunology
Anticorps bispécifiques
BCMA
Bispecific antibodies in multiple myeloma
Immunothérapie
Journal
Bulletin du cancer
ISSN: 1769-6917
Titre abrégé: Bull Cancer
Pays: France
ID NLM: 0072416
Informations de publication
Date de publication:
Oct 2021
Oct 2021
Historique:
received:
12
07
2021
revised:
17
10
2021
accepted:
18
10
2021
entrez:
18
12
2021
pubmed:
19
12
2021
medline:
30
12
2021
Statut:
ppublish
Résumé
Immunotherapies have recently emerged as potential game changers in the treatment of multiple myeloma (MM). Those include monoclonal antibodies (targeting CD38 or CS1), bispecific antibodies (BsAb, mainly targeting BCMA, GPRC5D or FcRH5), antibody-drug conjugate (mainly targeting BCMA) and CAR-T cells (mainly targeting BCMA). BsAb have the capacity to bind two different antigens, one at the tumor cell surface and one on T cells (CD3), recreating the immune synapse. In this article, we discuss the main clinical data on BsAb in MM, as well as their different constructs and the potential mechanism of resistance.
Identifiants
pubmed: 34920804
pii: S0007-4551(21)00434-3
doi: 10.1016/j.bulcan.2021.10.003
pii:
doi:
Substances chimiques
Antibodies, Bispecific
0
Antigens, Neoplasm
0
FCRL5 protein, human
0
GPRC5D protein, human
0
Receptors, Fc
0
Receptors, G-Protein-Coupled
0
SLAMF7 protein, human
0
Signaling Lymphocytic Activation Molecule Family
0
ADP-ribosyl Cyclase 1
EC 3.2.2.6
Types de publication
Journal Article
Review
Langues
fre
Sous-ensembles de citation
IM
Pagination
S205-S212Informations de copyright
Copyright © 2021 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.