Literature DB >> 9867127

Spontaneous occurrence of anti-fibrillin-1 autoantibodies in tight-skin mice.

C Murai1, S Saito, K N Kasturi, C A Bona.   

Abstract

Tight-skin (TSK) mouse represents an experimental for systemic sclerosis, displaying cutaneous hyperplasia, connective tissue alterations in the internal organs and developing autoantibodies against several scleroderma target autoantigens. TSK mouse syndrome is associated with a mutation in fibrillin-1 (Fbn-1), the major component of 10 nm microfibrils. Here, we have investigated whether TSK mouse develops autoimmunity to Fbn-1 similar to scleroderma target autoantigens. Our results show that anti-Fbn-1 IgG autoantibodies are present in high titer in many TSK mice. Specificity of these antibodies was confirmed by competitive inhibition assays and Western blotting analysis using recombinant human Fbn-1 protein. TSK mouse autoantibodies recognize a conserved epitope present in the C region of Fbn-1. These results indicate the presence of Fbn-1 specific T and B cells in TSK mouse repertoire.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9867127     DOI: 10.3109/08916939808996283

Source DB:  PubMed          Journal:  Autoimmunity        ISSN: 0891-6934            Impact factor:   2.815


  14 in total

Review 1.  The genetics of systemic sclerosis.

Authors:  Randall W Johnson; Monty B Tew; Frank C Arnett
Journal:  Curr Rheumatol Rep       Date:  2002-04       Impact factor: 4.592

2.  B-lymphocyte depletion reduces skin fibrosis and autoimmunity in the tight-skin mouse model for systemic sclerosis.

Authors:  Minoru Hasegawa; Yasuhito Hamaguchi; Koichi Yanaba; Jean-David Bouaziz; Junji Uchida; Manabu Fujimoto; Takashi Matsushita; Yukiyo Matsushita; Mayuka Horikawa; Kazuhiro Komura; Kazuhiko Takehara; Shinichi Sato; Thomas F Tedder
Journal:  Am J Pathol       Date:  2006-09       Impact factor: 4.307

3.  Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.

Authors:  B L Loeys; E E Gerber; D Riegert-Johnson; S Iqbal; P Whiteman; V McConnell; C R Chillakuri; D Macaya; P J Coucke; A De Paepe; D P Judge; F Wigley; E C Davis; H J Mardon; P Handford; D R Keene; L Y Sakai; H C Dietz
Journal:  Sci Transl Med       Date:  2010-03-17       Impact factor: 17.956

4.  CD19-dependent B lymphocyte signaling thresholds influence skin fibrosis and autoimmunity in the tight-skin mouse.

Authors:  Eriko Saito; Manabu Fujimoto; Minoru Hasegawa; Kazuhiro Komura; Yasuhito Hamaguchi; Yuko Kaburagi; Tetsuya Nagaoka; Kazuhiko Takehara; Thomas F Tedder; Shinichi Sato
Journal:  J Clin Invest       Date:  2002-06       Impact factor: 14.808

Review 5.  Molecular aspects of regulation of collagen gene expression in fibrosis.

Authors:  Rashpal K Bhogal; Cristina M Stoica; Tracy L McGaha; Constantin A Bona
Journal:  J Clin Immunol       Date:  2005-11       Impact factor: 8.317

Review 6.  Genetic and immunologic features associated with scleroderma-like syndrome of TSK mice.

Authors:  S Saito; K Kasturi; C Bona
Journal:  Curr Rheumatol Rep       Date:  1999-10       Impact factor: 4.592

7.  Polymorphism of immunoglobulin enhancer element HS1,2A: allele *2 associates with systemic sclerosis. Comparison with HLA-DR and DQ allele frequency.

Authors:  D Frezza; V Giambra; B Tolusso; M De Santis; S Bosello; S Vettori; G Triolo; G Valentini; G Ferraccioli
Journal:  Ann Rheum Dis       Date:  2007-03-28       Impact factor: 19.103

Review 8.  Autoimmunity in systemic sclerosis: current concepts.

Authors:  Francesco Boin; Antony Rosen
Journal:  Curr Rheumatol Rep       Date:  2007-05       Impact factor: 4.592

9.  Autoantibodies to a collagen-specific molecular chaperone, heat-shock protein 47, in systemic sclerosis.

Authors:  M Fujimoto; Y Hamaguchi; N Yazawa; K Komura; K Takehara; S Sato
Journal:  Clin Exp Immunol       Date:  2004-12       Impact factor: 4.330

Review 10.  Fibrillin-1 protein in tight skin mice and scleroderma.

Authors:  C Bona; S Saito
Journal:  Clin Rev Allergy Immunol       Date:  2000-02       Impact factor: 10.817

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.