Impaired b cell proliferation by Staphylococcus aureus Cowan 1 in patients with systemic lupus erythematosus
β Scribed by Shigemasa Sawada; Satoshi Amaki; Masami Takei; Miki Karasaki; Ichita Amaki
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 713 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0004-3591
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β¦ Synopsis
We examined the proliferative response to Staphylococcus aureus Cowan 1 (SAC) by enriched peripheral blood B cells from patients with systemic lupus erythematosus (SLE). Responses of B cells from patients with active and inactive SLE were significantly lower than those of B cells from normal individuals. Hyporesponsiveness to SAC was not observed in healthy family members of SLE patients. This hyporesponsiveness did not correlate with prednisolone therapy and could not be attributed to serum factors; it did correlate with the presence of suppressor monocytes. However, we could not exclude the possibility of enhanced sensitivity of SLE B lymphocytes to suppressive signals delivered by the monocytes.
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by aberrant functioning of immunocompetent cells, high titers of autoantibodies, and hypergammaglobulinemia. Recently, it has been found that unstimulated peripheral blood lymphocytes (PBL) from patients with SLE synthesize increased amounts of immunoglobulins and of antibodies to hapten or DNA in short-term culture From the
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## Abstract ## Objective Beta 1 integrin is a representative adhesion molecule for cellβcell and cellβextracellular matrix interactions, and it provides costimulatory signals to T cells. However, the relevance of Ξ²1 integrin to T cell activation in systemic lupus erythematosus (SLE) remains unclea