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• W1917304705 startingPage "1036" @default.
• W1917304705 abstract "The role of complement C3 in mediating systemic lupus erythematosus (SLE) was examined using a double-knockout C3(null)C4(null) Fas (CD95)-deficient mouse model. Results from this study reveal significant lymphadenopathy, splenomegaly, elevated titers of anti-nuclear Abs and anti-dsDNA Abs, an increased number of anti-dsDNA-producing cells in ELISPOT assay, as well as severe glomerulonephritis in the double-deficient mice. Based on these clinical, serological, and histological parameters, we find that autoimmune disease in the double-knockout group is similar in severity to that in C4(null) lpr mice, but not to that in C3(null) lpr mice. The development of severe SLE in the absence of both classical and alternative complement pathways suggests that it is the absence of C4, and not the presence of C3, that is critical in SLE pathogenesis. Thus, complement C4 provides an important protective role against the development of SLE." @default.
• W1917304705 created "2016-06-24" @default.
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• W1917304705 date "2002-02-01" @default.
• W1917304705 modified "2023-10-15" @default.
• W1917304705 title "Complement C4 Is Protective for Lupus Disease Independent of C3" @default.
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• W1917304705 doi "https://doi.org/10.4049/jimmunol.168.3.1036" @default.
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