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Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease
Autoimmunity may contribute to the pathogenesis of chronic obstructive pulmonary disease (COPD). Studies have identified disease-specific autoantibodies (DSAAbs) in COPD patients, but natural autoantibodies (NAAbs) may also play a role. Previous studies have concentrated on circulating autoantibodie...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367103/ https://www.ncbi.nlm.nih.gov/pubmed/25469980 http://dx.doi.org/10.1111/cei.12565 |
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author | Daffa, N I Tighe, P J Corne, J M Fairclough, L C Todd, I |
author_facet | Daffa, N I Tighe, P J Corne, J M Fairclough, L C Todd, I |
author_sort | Daffa, N I |
collection | PubMed |
description | Autoimmunity may contribute to the pathogenesis of chronic obstructive pulmonary disease (COPD). Studies have identified disease-specific autoantibodies (DSAAbs) in COPD patients, but natural autoantibodies (NAAbs) may also play a role. Previous studies have concentrated on circulating autoantibodies, but lung-associated autoantibodies may be most important. Our aim was to investigate NAAbs and DSAAbs in the circulation and lungs of COPD smoking (CS) patients compared to smokers (S) without airway obstruction and subjects who have never smoked (NS). Immunoglobulin (Ig)G antibodies that bind to lung tissue components were significantly lower in the circulation of CS patients than NS (with intermediate levels in S), as detected by enzyme-linked immunosorbent assay (ELISA). The levels of antibodies to collagen-1 (the major lung collagen) detected by ELISA were also reduced significantly in CS patients’ sera compared to NS. The detection of these antibodies in NS subjects indicates that they are NAAbs. The occurrence of DSAAbs in some CS patients and S subjects was indicated by high levels of serum IgG antibodies to cytokeratin-18 and collagen-5; furthermore, antibodies to collagen-5 eluted from homogenized lung tissue exposed to low pH (0·1 M glycine, pH 2·8) were raised significantly in CS compared to S and NS. Thus, this study supports a role in COPD for both NAAbs and DSAAbs. |
format | Online Article Text |
id | pubmed-4367103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43671032015-03-25 Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease Daffa, N I Tighe, P J Corne, J M Fairclough, L C Todd, I Clin Exp Immunol Original Articles Autoimmunity may contribute to the pathogenesis of chronic obstructive pulmonary disease (COPD). Studies have identified disease-specific autoantibodies (DSAAbs) in COPD patients, but natural autoantibodies (NAAbs) may also play a role. Previous studies have concentrated on circulating autoantibodies, but lung-associated autoantibodies may be most important. Our aim was to investigate NAAbs and DSAAbs in the circulation and lungs of COPD smoking (CS) patients compared to smokers (S) without airway obstruction and subjects who have never smoked (NS). Immunoglobulin (Ig)G antibodies that bind to lung tissue components were significantly lower in the circulation of CS patients than NS (with intermediate levels in S), as detected by enzyme-linked immunosorbent assay (ELISA). The levels of antibodies to collagen-1 (the major lung collagen) detected by ELISA were also reduced significantly in CS patients’ sera compared to NS. The detection of these antibodies in NS subjects indicates that they are NAAbs. The occurrence of DSAAbs in some CS patients and S subjects was indicated by high levels of serum IgG antibodies to cytokeratin-18 and collagen-5; furthermore, antibodies to collagen-5 eluted from homogenized lung tissue exposed to low pH (0·1 M glycine, pH 2·8) were raised significantly in CS compared to S and NS. Thus, this study supports a role in COPD for both NAAbs and DSAAbs. BlackWell Publishing Ltd 2015-04 2015-03-10 /pmc/articles/PMC4367103/ /pubmed/25469980 http://dx.doi.org/10.1111/cei.12565 Text en © 2014 The Authors. Clinical and Experimental Immunology published by John Wiley & Sons Ltd on behalf of British Society for Immunology. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Daffa, N I Tighe, P J Corne, J M Fairclough, L C Todd, I Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease |
title | Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease |
title_full | Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease |
title_fullStr | Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease |
title_full_unstemmed | Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease |
title_short | Natural and disease-specific autoantibodies in chronic obstructive pulmonary disease |
title_sort | natural and disease-specific autoantibodies in chronic obstructive pulmonary disease |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367103/ https://www.ncbi.nlm.nih.gov/pubmed/25469980 http://dx.doi.org/10.1111/cei.12565 |
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