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Spontaneously proliferating human B lymphocytes make autoantibodies.
G P Allaway1, J Srinivasappa, F W Miller
1Laboratory of Oral Medicine, National Institute of Dental Research, Bethesda, Maryland 20892.
The Journal of Infectious Diseases
|May 1, 1988
Summary
Latent Epstein-Barr virus (EBV) infection in patients with autoimmune diseases can lead to the production of autoantibodies. This study found that EBV reactivation in vitro correlates with autoantibody generation, suggesting a link to autoimmune disorders.
Area of Science:
- Immunology
- Virology
- Autoimmunity
Background:
- Autoimmune diseases are characterized by the immune system attacking the body's own tissues.
- Epstein-Barr virus (EBV) is a common human herpesvirus that establishes lifelong latent infections.
- The role of latent viral infections in the development of autoimmune disorders remains an area of active research.
Purpose of the Study:
- To investigate the potential link between latent Epstein-Barr virus (EBV) infection and autoantibody production in patients with autoimmune diseases.
- To determine if EBV reactivation in vitro can induce the generation of autoantibodies.
Main Methods:
- Peripheral blood lymphocytes from autoimmune patients and healthy controls were cultured in vitro.
- Lymphocyte proliferation and cell line establishment were monitored.
- Presence of EBV nuclear antigen confirmed latent EBV infection.
- Culture supernatants were screened for autoantibodies against normal tissues.
Main Results:
- Lymphocyte outgrowth occurred only in cultures from patients with antibodies to EBV viral capsid antigen.
- Proliferating cells contained EBV nuclear antigen, indicating latent EBV infection.
- Approximately 30% of established cell lines produced autoantibodies, some reacting with smooth muscle or epithelial cells.
Conclusions:
- Latent EBV infection in patients with autoimmune diseases can be reactivated in vitro.
- Reactivated EBV infection is associated with the production of autoantibodies.
- In vivo reactivation of latent EBV may contribute to autoantibody production in various immunoregulatory disorders.