[SLAM family proteins as therapeutic targets in multiple myeloma].


Journal

[Rinsho ketsueki] The Japanese journal of clinical hematology
ISSN: 0485-1439
Titre abrégé: Rinsho Ketsueki
Pays: Japan
ID NLM: 2984782R

Informations de publication

Date de publication:
2020
Historique:
entrez: 8 8 2020
pubmed: 8 8 2020
medline: 25 9 2020
Statut: ppublish

Résumé

Reports have described the excellent efficacies of new immunotherapeutic strategies, such as monoclonal antibody (mAb) therapies, in multiple myeloma (MM) patients. Signaling lymphocytic activation molecule family (SLAMF) molecules are expressed strongly on normal lymphocytes and plasma cells from MM patients. The anti-SLAMF7 mAb elotuzumab (ELO) has been approved for the treatment of relapsed/refractory MM (RRMM). In MM patients, a high serum soluble SLAMF7 (sSLAMF7) concentration is associated with aggressive clinical characteristics. This suggests a proliferative function of the SLAMF7-sSLAMF7 interaction that could be inhibited by ELO. SLAMF3 is also expressed strongly and constitutively on myeloma cells. We observed the aggressive characteristics of SLAMF3

Identifiants

pubmed: 32759570
doi: 10.11406/rinketsu.61.818
doi:

Substances chimiques

Antibodies, Monoclonal 0
Signaling Lymphocytic Activation Molecule Family Member 1 169535-43-7

Types de publication

Journal Article

Langues

jpn

Sous-ensembles de citation

IM

Pagination

818-826

Auteurs

Hideto Tamura (H)

Department of Hematology, Nippon Medical School.

Mariko Ishibashi (M)

Department of Microbiology and Immunology, Nippon Medical School.

Hidemi Takahashi (H)

Department of Microbiology and Immunology, Nippon Medical School.

Koiti Inokuchi (K)

Department of Hematology, Nippon Medical School.

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Classifications MeSH