Mechanisms of polyclonal B-cell activation in autoimmune B6- lpr/lpr mice

• Published in: Cellular immunology Vol. 84; no. 1; pp. 22 - 31
• Main Authors: Warren, Robert W., Roths, John B., Murphy, Edwin D., Pisetsky, David S.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01.03.1984
• Subjects: alpha-Macroglobulins - physiology; Animals; Autoantibodies - biosynthesis; Autoimmune Diseases - genetics; Autoimmune Diseases - immunology; B-Lymphocytes - immunology; Binding, Competitive; DNA, Single-Stranded - immunology; DNA, Single-Stranded - metabolism; Female; Humans; Immunoglobulin G - immunology; Lipopolysaccharides - pharmacology; Lymphocyte Activation; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Poly T - pharmacology; Sex Characteristics
• ISSN: 0008-8749; 1090-2163
• DOI: 10.1016/0008-8749(84)90073-X

The influence of the lpr gene on spontaneous and lipopolysaccharide (LPS)-induced immunoglobulin production was studied in B6 mice homozygous for the mutant lpr gene (B6- lpr/lpr). Male and female mice of this congenic strain were followed for 1 year and sera serially tested by the enzyme-linked immunosorbent assay (ELISA) for the production of antibodies to single-stranded DNA (anti-sDNA), immunoglobulin (anti-lgG), and keyhole limpet hemocyanin (anti-KLH), models of autoantibody and non-autoantibody responses, respectively. Female B6- lpr/lpr mice demonstrated marked spontaneous responses to all three antigens; the responses of male B6- lpr/lpr mice were significantly lower but still exceeded those of the congenic B6-+/+ controls. These results demonstrate a generalized influence of sex on lpr associated responses. To determine whether this sex difference could be demonstrated with other forms of B-cell activation, young B6-+/+ and B6- lpr/lpr male and female mice were immunized with lipopolysaccharide and the induced responses determined. This immunization caused significant increases in the IgM response only. The levels of the induced responses produced after LPS treatment were comparable for +/+ and lpr/lpr mice. These results indicate that the enhanced responsiveness of female mice to lpr action is not reflected in the polyclonal response to LPS, which, furthermore, was unaffected by the presence of lpr. The differential influence of sex on lpr and LPS-induced responses and their apparent independence suggests that lpr and LPS promote B-cell activation by dissimilar mechanisms.