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Updated: Aug 12, 2026

Establishment of a Human Multiple Myeloma Xenograft Model in the Chicken to Study Tumor Growth, Invasion and Angiogenesis
Published on: May 1, 2015
CD52 is not a promising immunotherapy target for most patients with multiple myeloma
Jörg Westermann1, Georg Maschmeyer, Antje van Lessen
1Department of Hematology and Oncology, Charité University Medicine Berlin, Campus Virchow Klinikum, Berlin, Germany. joerg.westermann@charite.de
Abstract:
The aim of our study was to evaluate CD52 as a target molecule for antibody therapy for multiple myeloma. Twenty consecutive bone marrow samples from myeloma patients were studied by flow cytometry using antibodies against CD45, CD38, CD138, CD3, CD19, and CD52. Most myeloma cells did not express CD52; CD52 expression was found only in a small subpopulation of plasma cells with a CD45+CD38++ phenotype. In contrast, the major fraction of myeloma cells (CD45-CD38++) was CD52-. Treatment of myeloma patients with anti-CD52 antibodies with the aim to reduce the number of myeloma cells in the CD45+CD38++ subfraction, which possibly contains a proliferative progenitor cell pool, would be at best a highly experimental approach. We conclude that CD52 is not a promising target for antibody-based therapies for most patients with multiple myeloma.
Insights
CD52 is not a promising target for multiple myeloma antibody therapy. Most myeloma cells do not express CD52, limiting the effectiveness of treatments targeting this molecule.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Multiple myeloma is a cancer of plasma cells.
- Identifying effective molecular targets for antibody therapy is crucial for improving patient outcomes.
- CD52 is a cell surface antigen that has been targeted in other hematological malignancies.
Purpose of the Study:
- To evaluate the expression of CD52 on multiple myeloma cells.
- To determine the potential of CD52 as a target for antibody-based therapies in multiple myeloma.
Main Methods:
- Bone marrow samples from 20 multiple myeloma patients were analyzed.
- Flow cytometry was used to assess the expression of CD45, CD38, CD138, CD3, CD19, and CD52 on myeloma cells.
Main Results:
- The majority of multiple myeloma cells (CD45-CD38++) did not express CD52.
- CD52 expression was detected only in a small subpopulation of plasma cells (CD45+CD38++).
- This CD52-expressing subpopulation may represent a proliferative progenitor cell pool.
Conclusions:
- CD52 is not a suitable molecular target for antibody therapy in most multiple myeloma patients.
- Targeting CD52 in multiple myeloma would be a highly experimental approach with limited efficacy.
- Further research is needed to identify more effective therapeutic targets for multiple myeloma.
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