Literature DB >> 6213030

Mitogenic responses to lipopolysaccharide by B lymphocytes from patients with systemic lupus erythematosus.

T Abe, T Toguchi, T Takeuchi, M Kiyotaki, M Homma.   

Abstract

Peripheral blood lymphocytes from 43 patients with systemic lupus erythematosus (SLE) and from age- and sex-matched normal controls were cultured with lipopolysaccharide (LPS) to examine the response to the polyclonal B-cell activator. Lymphocytes from active SLE patients incorporated 4840 +/- 471 (mean +/- SE) cpm in response to LPS, whereas lymphocytes from inactive SLE patients incorporated 6906 +/- 897 cpm. In contrast, lymphocytes from normal individuals incorporated 7452 +/- 1126 cpm. Ig synthesis of lymphocytes from active SLE in response to LPS stimulation was also less than that of normal individuals. The helper T-cell function of active SLE, as examined by co-culturing irradiated SLE lymphocytes with unirradiated normal lymphocytes, was normal. These results thus suggested that a defect of B lymphocytes exists in active SLE patients. This B-cell defect and T suppressor cells apparently play an important role in the pathogenesis of SLE.

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Year:  1981        PMID: 6213030     DOI: 10.1111/j.1365-3083.1982.tb00673.x

Source DB:  PubMed          Journal:  Scand J Immunol        ISSN: 0300-9475            Impact factor:   3.487


  1 in total

1.  Cutting edge: regulation of TLR4-driven B cell proliferation by RP105 is not B cell autonomous.

Authors:  Jessica L Allen; Leah M Flick; Senad Divanovic; Shaun W Jackson; Richard Bram; David J Rawlings; Fred D Finkelman; Christopher L Karp
Journal:  J Immunol       Date:  2012-01-30       Impact factor: 5.422

  1 in total

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