Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitis

<p>Abstract</p> <p>Background</p> <p>The pathogenetic mechanisms that underlie the interstitial lung disease cryptogenic fibrosing alveolitis (CFA) may involve an immunological reaction to unidentified antigens in the lung, resulting in tissue damage.</p> <p>...

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Main Authors: Lake Richard A, Robinson Bruce WS, Stevenson Sandra, Callow Marinella, Robinson Cleo
Format: Article
Language:English
Published: BMC 2001-02-01
Series:Respiratory Research
Subjects:
Online Access:http://dx.doi.org/10.1186/rr46
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author Lake Richard A
Robinson Bruce WS
Stevenson Sandra
Callow Marinella
Robinson Cleo
author_facet Lake Richard A
Robinson Bruce WS
Stevenson Sandra
Callow Marinella
Robinson Cleo
author_sort Lake Richard A
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The pathogenetic mechanisms that underlie the interstitial lung disease cryptogenic fibrosing alveolitis (CFA) may involve an immunological reaction to unidentified antigens in the lung, resulting in tissue damage.</p> <p>Method</p> <p>In order to identify the range of target autoantigens, we used expression cloning, employing serum from an index patient as the probe against an expressed cDNA library that was derived from a tumour cell line. We screened over 5 × 10<sup>5</sup> recombinants and obtained sequence information on three antigens that had provoked strong responses with immunoglobulin heavy chain class switching, presumably as a consequence of T-cell recognition.</p> <p>Results</p> <p>All of the antigens were identifiable by comparison with sequence data from the US National Center for Biotechnology Information. Alanyl tRNA synthetase (ATS) was picked on six occasions; five of these incidences reflected independent recombination events, indicating that the library was not biased. Antibodies to ATS (anti-PL-12) represent the most common reactivity that defines the antisynthetase syndrome, which is typically expressed as polymyositis, dermatomyositis and interstitial lung disease (ILD). The index patient never showed symptoms other than those associated with alveolitis, even though sera obtained from him over a period of 2 years contained antibodies with the same specificity. Autoantibodies to ATS were never detected in serial bleeds from 11 other patients with CFA, and neither did we detect antibodies to the other two antigens identified from the serum of the index patient.</p> <p>Conclusion</p> <p>The humoral response in patients with CFA can be dominated by autoantibodies with private specificities. This suggests that the antibodies are epiphenomenal and are a secondary feature of tissue damage induced by some other mechanism.</p>
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spelling doaj.art-2ff2fa21c091441da627e73a761c960b2022-12-22T03:08:36ZengBMCRespiratory Research1465-99212001-02-012211912410.1186/rr46Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitisLake Richard ARobinson Bruce WSStevenson SandraCallow MarinellaRobinson Cleo<p>Abstract</p> <p>Background</p> <p>The pathogenetic mechanisms that underlie the interstitial lung disease cryptogenic fibrosing alveolitis (CFA) may involve an immunological reaction to unidentified antigens in the lung, resulting in tissue damage.</p> <p>Method</p> <p>In order to identify the range of target autoantigens, we used expression cloning, employing serum from an index patient as the probe against an expressed cDNA library that was derived from a tumour cell line. We screened over 5 × 10<sup>5</sup> recombinants and obtained sequence information on three antigens that had provoked strong responses with immunoglobulin heavy chain class switching, presumably as a consequence of T-cell recognition.</p> <p>Results</p> <p>All of the antigens were identifiable by comparison with sequence data from the US National Center for Biotechnology Information. Alanyl tRNA synthetase (ATS) was picked on six occasions; five of these incidences reflected independent recombination events, indicating that the library was not biased. Antibodies to ATS (anti-PL-12) represent the most common reactivity that defines the antisynthetase syndrome, which is typically expressed as polymyositis, dermatomyositis and interstitial lung disease (ILD). The index patient never showed symptoms other than those associated with alveolitis, even though sera obtained from him over a period of 2 years contained antibodies with the same specificity. Autoantibodies to ATS were never detected in serial bleeds from 11 other patients with CFA, and neither did we detect antibodies to the other two antigens identified from the serum of the index patient.</p> <p>Conclusion</p> <p>The humoral response in patients with CFA can be dominated by autoantibodies with private specificities. This suggests that the antibodies are epiphenomenal and are a secondary feature of tissue damage induced by some other mechanism.</p>http://dx.doi.org/10.1186/rr46antisynthetase syndromecryptogenic fibrosing alveolitisdiagnostic autoantibodies
spellingShingle Lake Richard A
Robinson Bruce WS
Stevenson Sandra
Callow Marinella
Robinson Cleo
Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitis
Respiratory Research
antisynthetase syndrome
cryptogenic fibrosing alveolitis
diagnostic autoantibodies
title Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitis
title_full Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitis
title_fullStr Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitis
title_full_unstemmed Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitis
title_short Private specificities can dominate the humoral response to self-antigens in patients with cryptogenic fibrosing alveolitis
title_sort private specificities can dominate the humoral response to self antigens in patients with cryptogenic fibrosing alveolitis
topic antisynthetase syndrome
cryptogenic fibrosing alveolitis
diagnostic autoantibodies
url http://dx.doi.org/10.1186/rr46
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