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IgG4-related disease: why high IgG4 and fibrosis?
The hallmarks of IgG4-related disease (IgG4-RD) are lymphoplasmacytic tissue infiltration with a predominance of IgG4-positive plasma cells, accompanied by fibrosis, obliterative phlebitis, dacryoadenitis, and elevated levels of IgG4. In a recent issue of Arthritis Research & Therapy, Tsuboi and...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672717/ https://www.ncbi.nlm.nih.gov/pubmed/23351335 http://dx.doi.org/10.1186/ar4122 |
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author | Koike, Takao |
author_facet | Koike, Takao |
author_sort | Koike, Takao |
collection | PubMed |
description | The hallmarks of IgG4-related disease (IgG4-RD) are lymphoplasmacytic tissue infiltration with a predominance of IgG4-positive plasma cells, accompanied by fibrosis, obliterative phlebitis, dacryoadenitis, and elevated levels of IgG4. In a recent issue of Arthritis Research & Therapy, Tsuboi and colleagues demonstrated that regulatory T (Treg) cell-and T helper 2 (Th2) cell-derived cytokines contribute to the pathogenesis of Mikulicz's disease, an activation pathway that appears to be common for IgG4-RD. Additional organ-specific factors may account for the different organ involvement of IgG4-RD. |
format | Online Article Text |
id | pubmed-3672717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36727172013-07-25 IgG4-related disease: why high IgG4 and fibrosis? Koike, Takao Arthritis Res Ther Editorial The hallmarks of IgG4-related disease (IgG4-RD) are lymphoplasmacytic tissue infiltration with a predominance of IgG4-positive plasma cells, accompanied by fibrosis, obliterative phlebitis, dacryoadenitis, and elevated levels of IgG4. In a recent issue of Arthritis Research & Therapy, Tsuboi and colleagues demonstrated that regulatory T (Treg) cell-and T helper 2 (Th2) cell-derived cytokines contribute to the pathogenesis of Mikulicz's disease, an activation pathway that appears to be common for IgG4-RD. Additional organ-specific factors may account for the different organ involvement of IgG4-RD. BioMed Central 2013 2013-01-25 /pmc/articles/PMC3672717/ /pubmed/23351335 http://dx.doi.org/10.1186/ar4122 Text en Copyright © 2013 BioMed Central Ltd |
spellingShingle | Editorial Koike, Takao IgG4-related disease: why high IgG4 and fibrosis? |
title | IgG4-related disease: why high IgG4 and fibrosis? |
title_full | IgG4-related disease: why high IgG4 and fibrosis? |
title_fullStr | IgG4-related disease: why high IgG4 and fibrosis? |
title_full_unstemmed | IgG4-related disease: why high IgG4 and fibrosis? |
title_short | IgG4-related disease: why high IgG4 and fibrosis? |
title_sort | igg4-related disease: why high igg4 and fibrosis? |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672717/ https://www.ncbi.nlm.nih.gov/pubmed/23351335 http://dx.doi.org/10.1186/ar4122 |
work_keys_str_mv | AT koiketakao igg4relateddiseasewhyhighigg4andfibrosis |