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Infectious mononucleosis: a polyclonal B cell transformation in vivo
The Journal of Infectious Diseases
|October 1, 1984
Summary
Epstein-Barr virus transforms B lymphocytes from mononucleosis patients into immunoglobulin-secreting cell lines. This study reveals diverse immunoglobulin production patterns in these transformed B cells, including monoclonal and aberrant secretions.
Area of Science:
- Immunology
- Virology
- Cell Biology
Background:
- Epstein-Barr virus (EBV) is known to infect and transform B lymphocytes.
- Infectious mononucleosis is a common clinical manifestation of primary EBV infection.
- Understanding B cell transformation by EBV is crucial for immunology and disease research.
Purpose of the Study:
- To investigate the immunoglobulin secretion profiles of B lymphocyte colonies spontaneously transformed by Epstein-Barr virus.
- To characterize the diversity of immunoglobulin gene expression in EBV-transformed B cells.
- To identify potential B cell phenotypes present during EBV infection.
Main Methods:
- Soft-agar culture was used to obtain spontaneous B lymphocyte colonies from peripheral blood of mononucleosis patients.
- Transformed colonies were propagated into distinct cell lines.
- Immunoglobulin secretion (heavy and light chains) was analyzed for each cell line.
Main Results:
- 44 out of 52 propagated cell lines produced complete, monoclonal immunoglobulins.
- Mu-chain (62%), gamma-chain (29%), and alpha-chain (9%) were the predominant heavy chains secreted.
- Kappa-chain (31) and gamma-chain (13) were the secreted light chains; one clone showed a pre-B cell phenotype (mu-heavy chain only).
- Seven lines exhibited aberrant immunoglobulin secretion (e.g., dual heavy or light chains).
Conclusions:
- Epstein-Barr virus can transform B lymphocytes in various stages of immunoglobulin gene expression.
- The study demonstrates the capacity of EBV to induce monoclonal immunoglobulin production and aberrant secretion patterns.
- These findings provide insights into B cell differentiation and transformation dynamics during EBV infection.