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Engagement of complement receptor 2 on the surface of B cells from patients with systemic lupus erythematosus contributes to the increased responsiveness to antigen stimulationDepartment of Medicine, Walter Reed Army Medical Center, Washington, DC, USA
Uniformed Services University of the Health Sciences, Bethesda, MD, USA
Department of Medicine, Walter Reed Army Medical Center, Washington, DC, USA; Department of Cellular Injury, Walter Reed Army Institute of Research, Silver Spring, MD, USA; WRAIR, Bldg 503, Rm 1A32 gtsokos{at}usa.net B cells from patients with systemic lupus erythematosus (SLE) display increased responses following cross-linking of the surface antigen receptor. We explored the possibility that the increased responses are at least partially due to simultaneous cross-linking of the complement receptor 2 (CR2). To this end, we stimulated fresh B cells from SLE patients with an anti-IgD antibody conjugated to the EpsteinBarr virus gp350 protein, which binds to CR2, and recorded the free intracytoplasmic calcium response during the first 10 min. Despite the fact that SLE B cells were found to express half as many surface CR2 as normal B cells, both peak responses and the percentage of responding cells were significantly increased in the former. These observations suggest that regulatory molecules such as CR2 are involved in the increased B cell responses in SLE patients. We propose that certain immune complexes that circulate in the sera of SLE patients that have anti-surface immunoglobulin specificities and are decorated with natural ligands of CR2, such as C3d, elicit and promote B cell overactivity.
Key Words: B lymphocytes B cell receptor calcium responses B cell overactivity complement receptor EpsteinBarr virus lymphocyte signaling
Lupus, Vol. 11, No. 5,
299-303 (2002) |
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