Literature DB >> 11465716

Autoreactive T cells to topoisomerase I in monozygotic twins discordant for systemic sclerosis.

M Kuwana1, C A Feghali, T A Medsger, T M Wright.   

Abstract

OBJECTIVE: To examine T and B cell responses to topoisomerase I (topo I) in a monozygotic twin pair discordant for systemic sclerosis (SSc).
METHODS: The peripheral blood T cell proliferative responses induced by topo I and in vitro anti-topo I antibody production in cultures of T and B cells were examined in an SSc patient with serum anti-topo I antibody and in her healthy monozygotic twin. Topo I-reactive T cell lines were generated from the twin pair and analyzed for antigenic specificity, major histocompatibility complex class II restriction, and T cell receptor (TCR) gene usage.
RESULTS: T cell proliferative responses to topo I were detected in both the SSc patient and her healthy twin, although the kinetics of the T cell response were accelerated in the patient compared with the healthy twin. The estimated frequency of circulating topo I-reactive T cells was 1/6,700 in the SSc patient and 1/39,000 in the healthy twin. Anti-topo I antibody production was observed in cultures of T and B cells from the SSc patient, but not in those from the healthy twin. When the cells from the twins were mixed in different combinations, T cells from the healthy twin did stimulate the SSc patient's B cells to produce anti-topo I antibody through a CD40-dependent mechanism. Topo I-reactive T cell lines generated from the twins had similar characteristics, including a CD4+ phenotype, restriction by HLA-DR, recognition of epitopes within amino acid residues 209-386 of topo I, and dominant usage of the TCR Vbeta20 gene segment.
CONCLUSION: These results indicate that topo I-reactive T cells were activated and clonally expanded in the SSc patient. However, there were no substantial differences in either phenotypic or functional properties of topo I-reactive T cells obtained from the SSc patient and those obtained from her healthy identical twin. It is likely, therefore, that the anti-topo I antibody response in the SSc patient is induced by in vivo activation of topo I-reactive T cells derived from the normal T cell repertoire.

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Year:  2001        PMID: 11465716     DOI: 10.1002/1529-0131(200107)44:7<1654::AID-ART288>3.0.CO;2-O

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


  7 in total

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Authors:  S Veeraraghavan; E A Renzoni; H Jeal; M Jones; J Hammer; A U Wells; C M Black; K I Welsh; R M du Bois
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Review 2.  The role of the acquired immune response in systemic sclerosis.

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3.  Definition of Naturally Processed Peptides Reveals Convergent Presentation of Autoantigenic Topoisomerase I Epitopes in Scleroderma.

Authors:  Eleni Tiniakou; Andrea Fava; Zsuzsanna H McMahan; Tara Guhr; Robert N O'Meally; Ami A Shah; Fredrick M Wigley; Robert N Cole; Francesco Boin; Erika Darrah
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Review 4.  The role of autoreactive T-cells in the pathogenesis of idiopathic thrombocytopenic purpura.

Authors:  Masataka Kuwana; Yasuo Ikeda
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5.  Insulin-like growth factor binding proteins 3 and 5 are overexpressed in idiopathic pulmonary fibrosis and contribute to extracellular matrix deposition.

Authors:  Joseph M Pilewski; Lixin Liu; Adam C Henry; Alycia V Knauer; Carol A Feghali-Bostwick
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6.  Genetic imprinting of autoantibody repertoires in systemic lupus erythematosus patients.

Authors:  G J Silverman; R Srikrishnan; K Germar; C S Goodyear; K A Andrews; E M Ginzler; B P Tsao
Journal:  Clin Exp Immunol       Date:  2008-05-28       Impact factor: 4.330

7.  Frequency of circulating topoisomerase-I-specific CD4 T cells predicts presence and progression of interstitial lung disease in scleroderma.

Authors:  Andrea Fava; Raffaello Cimbro; Fredrick M Wigley; Qing-Rong Liu; Antony Rosen; Francesco Boin
Journal:  Arthritis Res Ther       Date:  2016-05-04       Impact factor: 5.156

  7 in total

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