Literature DB >> 10616014

Autoantibodies to the extracellular matrix microfibrillar protein, fibrillin 1, in patients with localized scleroderma.

F C Arnett1, F K Tan, Y Uziel, R M Laxer, B R Krafchik, S Antohi, C Bona.   

Abstract

OBJECTIVE: Serum autoantibodies to fibrillin 1, the major component of microfibrils in the extracellular matrix, recently have been reported to occur in the tight skin mouse and in patients with systemic sclerosis, but not in patients with other connective tissue diseases. This study was undertaken to determine whether antifibrillin 1 antibodies could be detected in patients with localized forms of scleroderma.
METHODS: Sera from 50 patients with localized scleroderma (27 with linear scleroderma and 23 with morphea) and 51 normal controls were tested for IgG and IgM antifibrillin 1 autoantibodies, using a radioimmunoassay (RIA) and a human recombinant fibrillin 1 protein (rFbn-1).
RESULTS: Both in patients with linear scleroderma and in those with morphea, mean levels of IgM and IgG binding to rFbn-1 were significantly higher than in controls. Eight patients with linear scleroderma (30%) and 6 patients with morphea (26%) had IgG autoantibodies to fibrillin 1 (rFbn-1) by RIA, compared with 3 controls (6%) (P = 0.006 and P = 0.022, respectively). No correlations between antifibrillin 1 antibodies and active skin disease or antinuclear antibody positivity were found.
CONCLUSION: Autoantibodies to fibrillin 1 occur in patients with both forms of localized scleroderma (linear scleroderma and morphea). The clinical and pathogenetic significance of this autoimmune response remains to be determined.

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Year:  1999        PMID: 10616014     DOI: 10.1002/1529-0131(199912)42:12<2656::AID-ANR22>3.0.CO;2-N

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


  8 in total

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2.  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
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Review 3.  Scleroderma-like cutaneous syndromes.

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Journal:  Curr Rheumatol Rep       Date:  2002-04       Impact factor: 4.592

4.  Absence of autoantibodies against correctly folded recombinant fibrillin-1 protein in systemic sclerosis patients.

Authors:  Jürgen Brinckmann; Nico Hunzelmann; Ehab El-Hallous; Thomas Krieg; Lynn Y Sakai; Sven Krengel; Dieter P Reinhardt
Journal:  Arthritis Res Ther       Date:  2005-09-06       Impact factor: 5.156

5.  Transforming growth factor-β1 in plaque morphea.

Authors:  Aleksandra Dańczak-Pazdrowska; Michał J Kowalczyk; Beata Szramka-Pawlak; Justyna Gornowicz-Porowska; Aleksandra Szewczyk; Wojciech Silny; Marta Molińska-Glura; Anna Olewicz-Gawlik; Ryszard Zaba; Jakub Pazdrowski; Paweł Hrycaj
Journal:  Postepy Dermatol Alergol       Date:  2013-12-18       Impact factor: 1.837

Review 6.  The aryl hydrocarbon receptor: a review of its role in the physiology and pathology of the integument and its relationship to the tryptophan metabolism.

Authors:  Rowland Noakes
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7.  Systemic sclerosis sera affect fibrillin-1 deposition by dermal blood microvascular endothelial cells: therapeutic implications of cyclophosphamide.

Authors:  Marilisa Villano; Annalisa Borghini; Mirko Manetti; Erica Gabbrielli; Antonella Rossi; Piersante Sestini; Anna Milia; Francesca Nacci; Serena Guiducci; Marco Matucci-Cerinic; Lidia Ibba-Manneschi; Elisabetta Weber
Journal:  Arthritis Res Ther       Date:  2013-08-20       Impact factor: 5.156

8.  Assessing the response of morphea and limited scleroderma to tranilast: a small prospective study comparing topical corticosteroids to a combination of topical corticosteroids and tranilast.

Authors:  Rowland Noakes
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  8 in total

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