| Literature DB >> 31115879 |
Reham Ashour1,2, Masaki Ri3,4, Sanaa Shaker Aly2, Takashi Yoshida1, Takuto Tachita1,5, Takashi Kanamori1, Sho Aoki1, Shiori Kinoshita1, Tomoko Narita1, Haruhito Totani1, Ayako Masaki1, Asahi Ito1, Shigeru Kusumoto1, Hirokazu Komatsu1, Samar Mansour6, Abdelrahman A Elsaied2, Shinsuke Iida1.
Abstract
Monoclonal antibodies against surface antigens on MM cells, such as anti-SLAMF7 and anti-CD38 antibodies, represent an attractive therapeutic modality for the eradication of multiple myeloma (MM) cells. However, further exploration of target molecules is urgently needed for the development of more effective therapies. In the present study, we studied the expression of CD48 in a total of 74 primary MM samples derived from patients to evaluate SLAMF2 (CD48) as a candidate in mAb therapy for MM. Of 74 samples, 39 were subjected to SLAMF7 analysis. Most of the MM cells, defined as CD38 and CD138 double-positive cells, showed strong expression of CD48 or SLAMF7 independent of disease stage or treatment history. In these 39 samples, most MM cells showed expression of both SLAMF7 and CD48; however, several samples showed expression of either only CD48 or only SLAMF7, including seven cases that were only highly positive for SLAMF7, and five that were only highly positive for CD48. Our study demonstrates that the immune receptor CD48 is overexpressed on MM cells together with SLAMF7, and that CD48 may be considered as an alternative target for treatment of MM in cases showing weak expression of SLAMF7.Entities:
Keywords: CD48; Flow cytometry; Multiple myeloma; SLAMF
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Year: 2019 PMID: 31115879 DOI: 10.1007/s12185-019-02649-3
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490