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A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity
Well over six decades since its first description, the Rheumatoid Factor (RF)—autoantibodies recognizing Fc (constant) portion of IgG through their own Fab (antigen binding variable segments)—is believed to have come of age. Autoimmune pancreatitis is a unique form of pancreatitis, biologically char...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2249926/ https://www.ncbi.nlm.nih.gov/pubmed/18297131 http://dx.doi.org/10.1371/journal.pone.0001637 |
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author | Kawa, Shigeyuki Kitahara, Kei Hamano, Hideaki Ozaki, Yayoi Arakura, Norikazu Yoshizawa, Kaname Umemura, Takeji Ota, Masao Mizoguchi, Sadaaki Shimozuru, Yasunori Bahram, Seiamak |
author_facet | Kawa, Shigeyuki Kitahara, Kei Hamano, Hideaki Ozaki, Yayoi Arakura, Norikazu Yoshizawa, Kaname Umemura, Takeji Ota, Masao Mizoguchi, Sadaaki Shimozuru, Yasunori Bahram, Seiamak |
author_sort | Kawa, Shigeyuki |
collection | PubMed |
description | Well over six decades since its first description, the Rheumatoid Factor (RF)—autoantibodies recognizing Fc (constant) portion of IgG through their own Fab (antigen binding variable segments)—is believed to have come of age. Autoimmune pancreatitis is a unique form of pancreatitis, biologically characterized by an elevated serum IgG4 concentration. Given the fact that IgG4 myeloma proteins can act as RF, we initially hypothesized that IgG4 in autoimmune pancreatitis might do likewise, hence potentially contributing to disease pathogenesis. Indeed Western blotting clearly showed that IgG4 binds to IgG1 κ, IgG2 κ, IgG3 κ myeloma proteins, as well as to IgG Fc, in line with a typical RF activity. Further experiments however unraveled the unexpected fact that unlike hitherto known RF, IgG4 does not engage IgG Fc through its Fab, but its very own Fc. These data therefore collectively describe a Novel RF (NRF) in autoimmune pancreatitis. In the future, the relevance of NRF, beyond autoimmune pancreatitis, in both diagnosis/prognosis as well as pathophysiology of autoimmune and other systemic diseases where IgG4's role seems paramount, needs to be systematically assessed. |
format | Text |
id | pubmed-2249926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22499262008-02-23 A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity Kawa, Shigeyuki Kitahara, Kei Hamano, Hideaki Ozaki, Yayoi Arakura, Norikazu Yoshizawa, Kaname Umemura, Takeji Ota, Masao Mizoguchi, Sadaaki Shimozuru, Yasunori Bahram, Seiamak PLoS One Research Article Well over six decades since its first description, the Rheumatoid Factor (RF)—autoantibodies recognizing Fc (constant) portion of IgG through their own Fab (antigen binding variable segments)—is believed to have come of age. Autoimmune pancreatitis is a unique form of pancreatitis, biologically characterized by an elevated serum IgG4 concentration. Given the fact that IgG4 myeloma proteins can act as RF, we initially hypothesized that IgG4 in autoimmune pancreatitis might do likewise, hence potentially contributing to disease pathogenesis. Indeed Western blotting clearly showed that IgG4 binds to IgG1 κ, IgG2 κ, IgG3 κ myeloma proteins, as well as to IgG Fc, in line with a typical RF activity. Further experiments however unraveled the unexpected fact that unlike hitherto known RF, IgG4 does not engage IgG Fc through its Fab, but its very own Fc. These data therefore collectively describe a Novel RF (NRF) in autoimmune pancreatitis. In the future, the relevance of NRF, beyond autoimmune pancreatitis, in both diagnosis/prognosis as well as pathophysiology of autoimmune and other systemic diseases where IgG4's role seems paramount, needs to be systematically assessed. Public Library of Science 2008-02-20 /pmc/articles/PMC2249926/ /pubmed/18297131 http://dx.doi.org/10.1371/journal.pone.0001637 Text en Kawa et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kawa, Shigeyuki Kitahara, Kei Hamano, Hideaki Ozaki, Yayoi Arakura, Norikazu Yoshizawa, Kaname Umemura, Takeji Ota, Masao Mizoguchi, Sadaaki Shimozuru, Yasunori Bahram, Seiamak A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity |
title | A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity |
title_full | A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity |
title_fullStr | A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity |
title_full_unstemmed | A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity |
title_short | A Novel Immunoglobulin-Immunoglobulin Interaction in Autoimmunity |
title_sort | novel immunoglobulin-immunoglobulin interaction in autoimmunity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2249926/ https://www.ncbi.nlm.nih.gov/pubmed/18297131 http://dx.doi.org/10.1371/journal.pone.0001637 |
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