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Updated: Aug 11, 2025

Flow Cytometric Characterization of Murine B Cell Development
Published on: January 22, 2021
The exploration of B cell maturation antigen expression in plasma cell dyscrasias beyond multiple myeloma
Yanjie Xu1, Xia Mao1,2, Yimei Que1
1Department of Hematology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, 1095 Jie-Fang Avenue, Wuhan, Hubei, 430030, P. R. China.
Background:
B cell maturation antigen (BCMA) targeted immunotherapies have demonstrated remarkable clinical efficacy in multiple myeloma (MM). Here, we evaluated the BCMA expression in MM and other plasma cell dyscrasias (PCDs), hoping to provide a potential treatment strategy for the relapsed/refractory PCDs besides MM.
Methods:
From January 2018 to August 2021, 377 patients with PCDs were enrolled in this study, including 334 MM, 21 systemic light chain amyloidosis (AL), 5 POEMS syndrome, 14 monoclonal gammopathy of undetermined significance (MGUS), and three monoclonal gammopathy of renal significance (MGRS). The membrane-bound BCMA expression measured by multiparameter flow cytometry was defined by BCMA positivity rate and the mean fluorescence intensity (MFI).
Results:
The patients with MM had a median BCMA positive rate of 88.55% (range, 0.2% - 99.9%) and median BCMA MFI of 1281 (range, 109 - 48586). While the median BCMA positive rate in other PCDs was 55.8% (6.2% -98.9%), and the median BCMA MFI was 553 (182- 5930). BCMA expression level was negatively associated with hemoglobin concentration in multivariate analysis in terms of BCMA positive rate and MFI.
Conclusions:
In conclusion, BCMA has the potential to be a therapeutic target for other PCDs besides MM.
Insights
B cell maturation antigen (BCMA) is expressed in multiple myeloma (MM) and other plasma cell dyscrasias (PCDs). This suggests BCMA immunotherapies could treat a wider range of PCDs beyond MM.
Area of Science:
- Oncology
- Immunology
- Hematology
Background:
- B cell maturation antigen (BCMA) targeted immunotherapies show significant efficacy in multiple myeloma (MM).
- Evaluating BCMA expression in various plasma cell dyscrasias (PCDs) is crucial for expanding treatment strategies.
- Relapsed/refractory PCDs beyond MM require novel therapeutic targets.
Purpose of the Study:
- To assess BCMA expression levels across different types of PCDs.
- To determine if BCMA can serve as a therapeutic target for PCDs other than MM.
- To correlate BCMA expression with clinical parameters in PCD patients.
Main Methods:
- Analysis of 377 patients with PCDs (including MM, AL amyloidosis, POEMS, MGUS, MGRS) from January 2018 to August 2021.
- Quantification of membrane-bound BCMA expression using multiparameter flow cytometry, assessing positivity rate and mean fluorescence intensity (MFI).
- Multivariate analysis to identify associations between BCMA expression and clinical factors like hemoglobin concentration.
Main Results:
- Multiple myeloma patients exhibited a high median BCMA positive rate (88.55%) and MFI (1281).
- Other PCDs showed a median BCMA positive rate of 55.8% and MFI of 553.
- BCMA expression levels (positive rate and MFI) were found to be negatively correlated with hemoglobin concentration.
Conclusions:
- BCMA is expressed in various PCDs, indicating its potential as a therapeutic target beyond multiple myeloma.
- BCMA-targeted therapies may offer new treatment options for patients with relapsed/refractory PCDs.
- Further research into BCMA's role in PCDs is warranted to develop targeted immunotherapies.
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