Literature DB >> 310856

Palmerston North mice, a new animal model of systemic lupus erythematosus.

S E Walker, R H Gray, M Fulton, R D Wigley, B Schnitzer.   

Abstract

This report describes a previously unrecognized animal model of SLE, the PN mouse. Although outbred PN mice were studied originally as models of polyarteritis nodosa, their inbred descendants have autoimmune disease which closely resembles SLE. In the current study, positive indirect immunofluorescence tests for ANA appeared when the mice were 5 months old, and 80% of mice were ANA-positive at 10 months of age. Anti-DNA were detected in sera from newborn mice and from 53% of mice under 2 months of age. Seventy-six percent of PN mice developed anti-DNA at the age of 10 months. Glomerular deposits of IgG, IgM, IgA, and complement appeared at 2 to 4 weeks of age, and examination of renal tissue by electron microscopy showed basement membrane thickening and dense intramembranous deposits. Neoplasms arose in 14% of PN mice. Female mice died earlier than male mice, and the most common causes of death were glomerulonephritis and arteritis. It was concluded that the serologic and histologic characteristics of disease in PN mice resembled SLE.

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Year:  1978        PMID: 310856

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN: 0022-2143


  3 in total

1.  The H-2 haplotype of the PN (Palmerston North) inbred strain.

Authors:  J S Schultz; S E Walker; C S David
Journal:  Immunogenetics       Date:  1982       Impact factor: 2.846

2.  Further characterization of the autoantibody response of Palmerston North mice.

Authors:  B S Handwerger; C E Storrer; C S Wasson; F Movafagh; M Reichlin
Journal:  J Clin Immunol       Date:  1999-01       Impact factor: 8.317

3.  Tissue graft rejection in murine models of autoimmune disease.

Authors:  J Schultz; R Demott-Friberg; S Walker; T F Beals
Journal:  Clin Exp Immunol       Date:  1983-02       Impact factor: 4.330

  3 in total

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