Literature DB >> 3559205

Anti-RNA polymerase I antibodies: potential role in the induction and progression of murine lupus nephritis.

D A Stetler, T Cavallo.   

Abstract

Antibodies against RNA polymerase I were detected in plasma and kidney eluates of NZB/W mice. Plasma concentrations of the antibodies were the highest in mice with incipient nephritis and the lowest in mice with progressive nephritis. Mice with attenuated nephritis due to immunosuppressive therapy had intermediate plasma concentrations of the antibodies. The specific concentrations (ng/microgram IgG) of anti-RNA polymerase I antibodies in kidney eluates were significantly (10- to 70-fold) greater than the corresponding plasma concentrations. These results indicated that the decreased plasma concentration of the antibodies in mice with more advanced disease was at least partially due to selective concentration of anti-RNA polymerase I antibodies in the kidneys. The degree of this selective concentration was directly proportional (R2 = 0.9962) to the severity of renal disease, as reflected by the concentration (microgram/g tissue) of IgG eluted from the kidneys. The concentration (microgram/g tissue) of anti-RNA polymerase I eluted from the kidneys also was increased in mice with more severe renal disease. Further, the extent of this increase was greater than that of total IgG, again suggesting that anti-RNA polymerase I antibodies had been selectively concentrated in the kidneys. These findings are strongly suggestive of an important role for the RNA polymerase I/anti-RNA polymerase I antibody system in the pathogenesis of murine lupus nephritis.

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Year:  1987        PMID: 3559205

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  9 in total

1.  Prolonged circulation of immune complexes due to various altered immune functions contributes to nephritis in MRL/lpr mice.

Authors:  N A Granholm; T Cavallo
Journal:  Clin Exp Immunol       Date:  1990-11       Impact factor: 4.330

2.  Mapping of epitopes on U1 snRNP polypeptide A with synthetic peptides and autoimmune sera.

Authors:  S Barakat; J P Briand; N Abuaf; M H van Regenmortel; S Muller
Journal:  Clin Exp Immunol       Date:  1991-10       Impact factor: 4.330

3.  Analysis of antibodies to RNA in patients with systemic lupus erythematosus and other autoimmune rheumatic diseases.

Authors:  F Blanco; J Kalsi; D A Isenberg
Journal:  Clin Exp Immunol       Date:  1991-10       Impact factor: 4.330

4.  Presence of antibodies to ubiquitin during the autoimmune response associated with systemic lupus erythematosus.

Authors:  S Muller; J P Briand; M H Van Regenmortel
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

Review 5.  Clinical Significance of Antinucleolar Antibodies: Biomarkers for Autoimmune Diseases, Malignancies, and others.

Authors:  Minoru Satoh; Angela Ceribelli; Tomoko Hasegawa; Shin Tanaka
Journal:  Clin Rev Allergy Immunol       Date:  2022-03-08       Impact factor: 10.817

6.  Induction of an anti-Fab, anti-DNA and anti-RNA polymerase I autoantibody response network in rabbits immunized with SLE anti-DNA antibody.

Authors:  E Rombach; D A Stetler; J C Brown
Journal:  Clin Exp Immunol       Date:  1993-12       Impact factor: 4.330

7.  Serologic markers of lupus nephritis in patients: use of a tissue-based ELISA and evidence for immunopathogenic heterogeneity.

Authors:  K A Bernstein; L E Kahl; J E Balow; J B Lefkowith
Journal:  Clin Exp Immunol       Date:  1994-10       Impact factor: 4.330

8.  A branched, synthetic octapeptide of ubiquitinated histone H2A as target of autoantibodies.

Authors:  S Plaué; S Muller; M H van Regenmortel
Journal:  J Exp Med       Date:  1989-05-01       Impact factor: 14.307

Review 9.  Epigenetics of autoantigens: new opportunities for therapy of autoimmune diseases.

Authors:  Marko Radic; Sylviane Muller
Journal:  Genet Epigenet       Date:  2013-10-29
  9 in total

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