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Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that is accompanied by the emergence of autoreactive T cells and a reduction in regulatory T cells. Humans and mice with SLE have reduced numbers of CD1d-restricted NK T cells, suggesting a role for these cells in the regulation of SLE. In this study, we show that CD1d deficiency exacerbates lupus nephritis induced by the hydrocarbon oil pristane. This exacerbation in disease is associated with: 1) reduced TNF-alpha and IL-4 production by T cells, especially during the disease induction phase; and 2) expansion of marginal zone B cells. Strikingly, inoculation of pristane in wild-type mice resulted in reduced numbers and/or functions of NK T cells and CD1d-expressing dendritic cells. These findings suggest that CD1d may play an immunoregulatory role in the development of lupus in the pristane-induced model.

Original publication




Journal article


J Immunol

Publication Date





2142 - 2153


Adjuvants, Immunologic, Animals, Antigens, CD1, Antigens, CD1d, Autoantibodies, B-Lymphocyte Subsets, Cells, Cultured, Coculture Techniques, Cytokines, Disease Models, Animal, Down-Regulation, Galactosylceramides, Gene Deletion, Injections, Intraperitoneal, Killer Cells, Natural, Lupus Nephritis, Lymphocyte Activation, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Knockout, Species Specificity, T-Lymphocyte Subsets, T-Lymphocytes, Terpenes