Literature DB >> 6333245

Self-associating IgG rheumatoid factors in MRL/l autoimmune mice.

F A Nardella, D C Teller, S Izui, M Mannik.   

Abstract

Previous work has shown that the intermediate complexes isolated from the plasma of patients with rheumatoid arthritis are composed of self-associating IgG rheumatoid factors. Mice of the MRL/l strain develop spontaneous autoimmune disease with arthritis that is pathologically similar to human rheumatoid arthritis. Also, the sera of MRL/l mice contain autoantibodies to nuclear antigens as well as IgM and IgG rheumatoid factors. The present studies were done to determine if the IgG rheumatoid factors isolated from these mice undergo self-association. MRL/l mouse sera were categorized into groups A and B based on serum-serum precipitin interactions. Thirteen of 13 MRL/l mice sera examined contained intermediate complexes sedimenting between the 6.6S and 19S components of normal serum by sedimentation velocity ultracentrifugation. There were no differences in the level of intermediate complexes between groups A and B. IgG rheumatoid factors were isolated from the sera of 9 other mice. Upon sedimentation equilibrium ultracentrifugation, these rheumatoid factors underwent concentration-dependent self-association similar to that described for human self-associating IgG rheumatoid factors, although the precise stoichiometry of self-association could not be determined. The IgG rheumatoid factors from group B had higher energies of self-interaction than those from group A. These studies provide additional evidence that MRL/l mice may be the best available animal model for the study of human rheumatoid arthritis.

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Year:  1984        PMID: 6333245     DOI: 10.1002/art.1780271013

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  8 in total

1.  Experimental lupus nephritis in severe combined immunodeficient (SCID) mice: remodelling of the glomerular lesions by bystander IgM antibodies.

Authors:  M R Ito; S Terasaki; E Kondo; H Shiwaku; Y Fukuoka; M Nose
Journal:  Clin Exp Immunol       Date:  2000-02       Impact factor: 4.330

2.  Arteritis in a novel congenic strain of mice derived from MRL/Lpr lupus mice: genetic dissociation from glomerulonephritis and limited autoantibody production.

Authors:  M Nose; M Nishimura; M R Ito; J Toh; T Shibata; T Sugisaki
Journal:  Am J Pathol       Date:  1996-11       Impact factor: 4.307

3.  Connective tissue abnormalities in MRL/1 mice.

Authors:  J C Edwards; A Cooke; A R Moore; C Collins; F Hay; D A Willoughby
Journal:  Ann Rheum Dis       Date:  1986-06       Impact factor: 19.103

Review 4.  Possible role of microbial IgG Fc-binding proteins in rheumatoid arthritis.

Authors:  P Christensen; A K Schröder
Journal:  Agents Actions       Date:  1990-01

5.  Induction of different types of glomerulonephritis by monoclonal antibodies derived from an MRL/lpr lupus mouse.

Authors:  J Itoh; M Nose; S Takahashi; M Ono; S Terasaki; E Kondoh; M Kyogoku
Journal:  Am J Pathol       Date:  1993-11       Impact factor: 4.307

6.  IgG rheumatoid factors and cryoglobulins in mice bearing the mutant gene lpr (lymphoproliferation).

Authors:  S Izui; M Abdelmoula; Y Gyotoku; G Lange; P H Lambert
Journal:  Rheumatol Int       Date:  1984       Impact factor: 2.631

7.  Heterogeneity in rheumatoid factor isotypes and specificities in MRL mice.

Authors:  A Bond; A Cooke; F C Hay
Journal:  Immunology       Date:  1988-05       Impact factor: 7.397

8.  Effect of etodolac, a new nonsteroidal anti-inflammatory drug, in MRL/lpr mice with articular lesions.

Authors:  H Yoshida-Suzuka; Y Nakamura; Y Shibata; K Kimura
Journal:  Agents Actions       Date:  1991-07
  8 in total

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