Distinct clonotypes of anti-DNA antibodies in mice with lupus nephritis.
Open Access
- 1 August 1985
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 76 (2), 685-694
- https://doi.org/10.1172/jci112022
Abstract
Clonotypes of IgG anti-DNA antibodies were studied by isoelectric focusing in various autoimmune mice with or without lethal lupus nephritis. MRL/MpJ-lpr/lpr mice exhibited the most heterogeneous spectrotypes of anti-DNA antibodies in the pH range from 6.5 to 8.5, with marked variation in individual mice. Female (NZB X NZW)F1 mice expressed rather uniform DNA-binding bands composed of at least five to six distinct subgroups, having isoelectric points from 6.5 to 8.0. Male BXSB mice showed major characteristic bands confined to alkaline pH range from 7.8 to 8.5, similar to C57BL/6J-lpr/lpr mice, which showed markedly restricted bands in this region. Both AKR/J-lpr/lpr and C3H/HeJ-lpr/lpr mice expressed DNA-binding bands mostly focused between pH 6.5 and 8.2. The aging study indicated that three autoimmune mice (MRL/MpJ-lpr/lpr, [NZB X NZW]F1, and male BXSB) that developed fatal glomerulonephritis showed clonal expansion of anti-DNA antibodies throughout their life. In contrast, such age-dependent expansion of anti-DNA clonotypes was not evident in three lpr cogenic mice (C57BL/6J-lpr/lpr, AKR/J-lpr/lpr, and C3H/HeJ-lpr/lpr) that developed only mild glomerulonephritis; rather, their expression of anti-DNA spectrotypes diminished as they aged. Anti-DNA activities in renal eluates from nephritic autoimmune mice were mostly distributed in the pH range from 6.5 to 8.0, without significant concentrations in the high alkaline range of more than pH 8.0. These results suggest that there exist distinct anti-DNA clonotypes in each mouse strain and that the development of lupus nephritis does not appear to be associated with particular spectrotypes of anti-DNA antibodies. Rather, the age-dependent expansion of anti-DNA clonotypes may be a feature more characteristic of mice developing lethal lupus nephritis.This publication has 33 references indexed in Scilit:
- The influence of the lpr gene on B cell activation: Differential antibody expression in lpr congenic mouse strainsClinical Immunology and Immunopathology, 1984
- The in vivo and in vitro glomerular deposition of isolated anti-double-stranded-DNA antibodies in miceClinical Immunology and Immunopathology, 1984
- Quantitative studies of in situ immune complex glomerulonephritis in the rat induced by planted, cationized antigenThe Journal of Experimental Medicine, 1982
- Comparison of different antinucleic acid antibody spectrotypes in spontaneous, induced, and murine lupus.Journal of Clinical Investigation, 1981
- Circulating anti-DNA-rheumatoid factor complexes in miceClinical Immunology and Immunopathology, 1980
- Spontaneous murine lupus-like syndromes. Clinical and immunopathological manifestations in several strains.The Journal of Experimental Medicine, 1978
- Role of molecular charge in glomerular permeability. Tracer studies with cationized ferritins.The Journal of cell biology, 1975
- Prevention of Murine Lupus Nephritis by Carrier-Dependent Induction of Immunologic Tolerance to Denatured DNAScience, 1973
- ANTIBODIES TO POLYNUCLEOTIDES IN HUMAN SERA: ANTIGENIC SPECIFICITY AND RELATION TO DISEASEThe Journal of Experimental Medicine, 1971
- IMMUNOLOGICAL STUDIES CONCERNING THE NEPHRITIS OF SYSTEMIC LUPUS ERYTHEMATOSUSThe Journal of Experimental Medicine, 1967