Related Experiment Videos
A plasmocyte selective monoclonal antibody (B-B4) recognizes syndecan-1
J Wijdenes1, W C Vooijs, C Clément
1Diaclone, Besançon, France.
British Journal of Haematology
|August 1, 1996
Summary
A new monoclonal antibody, B-B4, specifically identifies human plasma cells, including those in multiple myeloma. This antibody, recognizing syndecan-1, is a valuable tool for diagnosing hematological malignancies and cell depletions.
Area of Science:
- Immunology
- Hematology
- Oncology
Background:
- Plasma cells are crucial in humoral immunity.
- Multiple myeloma is a hematological malignancy characterized by malignant plasma cells.
- Accurate identification of plasma cells is vital for diagnosis and treatment.
Purpose of the Study:
- To develop and characterize a novel monoclonal antibody for specific human plasma cell identification.
- To evaluate the utility of the new antibody in diagnosing multiple myeloma and other hematological malignancies.
- To explore the potential application of the antibody in cell-based therapies.
Main Methods:
- Development of a new monoclonal antibody, designated B-B4.
- Testing the reactivity of B-B4 against various human cell types, including multiple myeloma cell lines and patient samples.
- Immunohistochemical analysis of tumor samples.
- Antigen cloning to identify the target recognized by B-B4.
Main Results:
- The B-B4 antibody specifically identifies human plasma cells.
- B-B4 strongly reacts with multiple myeloma cell lines and malignant plasma cells from patients.
- No reactivity was observed with peripheral blood, bone marrow, or tonsil cells.
- The B-B4 antigen was identified as syndecan-1.
- The antibody showed potential for use in depletions prior to CD34 grafting.
Conclusions:
- The monoclonal antibody B-B4 is a suitable and specific marker for human plasma cells.
- B-B4 is a valuable tool for the diagnosis of hematological malignancies, particularly multiple myeloma.
- B-B4 has potential applications in cell-based therapies, such as prior to CD34 grafting.