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Updated: Apr 3, 2026

In Vitro Differentiation Model of Human Normal Memory B Cells to Long-lived Plasma Cells
Published on: January 20, 2019
Targeting B-cell maturation antigen in multiple myeloma
Yu-Tzu Tai1, Kenneth C Anderson1
1Jerome Lipper Multiple Myeloma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, 450 Brookline Ave, Boston, MA 02215, USA.
Novel immunotherapies targeting B-cell maturation antigen (BCMA) show promise for multiple myeloma (MM). Research reviews BCMA biology and highlights antibody-drug conjugates and CAR T-cells in ongoing clinical trials for relapsed and refractory MM.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Multiple myeloma (MM) recurrence necessitates novel immunotherapies.
- B-cell maturation antigen (BCMA) is a highly selective target on malignant plasma cells.
- BCMA-targeted therapies offer a promising avenue for MM treatment.
Purpose of the Study:
- To review BCMA biology and its relevance in multiple myeloma.
- To highlight the clinical development of novel anti-BCMA immunotherapies.
- To discuss ongoing clinical trials for BCMA-targeted treatments in MM.
Main Methods:
- Review of BCMA-related biological mechanisms.
- Highlighting the development of an afucosylated anti-BCMA monoclonal antibody (GSK2857916) with a cytotoxic payload.
- Discussion of chimeric antigen receptor (CAR) T-cell therapy targeting BCMA.
Main Results:
- BCMA is a validated target for MM therapy.
- Afucosylated anti-BCMA antibody-drug conjugates demonstrate potential efficacy.
- BCMA-targeted CAR T-cells may induce durable anti-MM responses.
Conclusions:
- BCMA-targeted immunotherapies, including antibody-drug conjugates and CAR T-cells, represent a significant advancement in MM treatment.
- Ongoing clinical trials are evaluating the safety and efficacy of these novel approaches.
- These therapies hold promise for patients with relapsed and refractory multiple myeloma.
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