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Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels
Multicentric Castleman Disease is largely driven by increased signaling in the pathway for the plasma cell growth factor interleukin-6. We hypothesized that interleukin-6/interleukin-6 receptor/gp130 polymorphisms contribute to increased interleukin-6 and/or other components of the interleukin-6 sig...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553080/ https://www.ncbi.nlm.nih.gov/pubmed/23372742 http://dx.doi.org/10.1371/journal.pone.0054610 |
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author | Stone, Katie Woods, Emily Szmania, Susann M. Stephens, Owen W. Garg, Tarun K. Barlogie, Bart Shaughnessy, John D. Hall, Brett Reddy, Manjula Hoering, Antje Hansen, Emily van Rhee, Frits |
author_facet | Stone, Katie Woods, Emily Szmania, Susann M. Stephens, Owen W. Garg, Tarun K. Barlogie, Bart Shaughnessy, John D. Hall, Brett Reddy, Manjula Hoering, Antje Hansen, Emily van Rhee, Frits |
author_sort | Stone, Katie |
collection | PubMed |
description | Multicentric Castleman Disease is largely driven by increased signaling in the pathway for the plasma cell growth factor interleukin-6. We hypothesized that interleukin-6/interleukin-6 receptor/gp130 polymorphisms contribute to increased interleukin-6 and/or other components of the interleukin-6 signaling pathway in HIV-negative Castleman Disease patients. The study group was composed of 58 patients and 50 healthy donors of a similar racial/ethnic profile. Of seven polymorphisms chosen for analysis, we observed an increased frequency between patients and controls of the minor allele of interleukin-6 receptor polymorphism rs4537545, which is in linkage disequilibrium with interleukin-6 receptor polymorphism rs2228145. Further, individuals possessing at least one copy of the minor allele of either polymorphism expressed higher levels of soluble interleukin-6 receptor. These elevated interleukin-6 receptor levels may contribute to increased interleukin-6 activity through the trans-signaling pathway. These data suggest that interleukin-6 receptor polymorphism may be a contributing factor in Castleman Disease, and further research is warranted. |
format | Online Article Text |
id | pubmed-3553080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35530802013-01-31 Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels Stone, Katie Woods, Emily Szmania, Susann M. Stephens, Owen W. Garg, Tarun K. Barlogie, Bart Shaughnessy, John D. Hall, Brett Reddy, Manjula Hoering, Antje Hansen, Emily van Rhee, Frits PLoS One Research Article Multicentric Castleman Disease is largely driven by increased signaling in the pathway for the plasma cell growth factor interleukin-6. We hypothesized that interleukin-6/interleukin-6 receptor/gp130 polymorphisms contribute to increased interleukin-6 and/or other components of the interleukin-6 signaling pathway in HIV-negative Castleman Disease patients. The study group was composed of 58 patients and 50 healthy donors of a similar racial/ethnic profile. Of seven polymorphisms chosen for analysis, we observed an increased frequency between patients and controls of the minor allele of interleukin-6 receptor polymorphism rs4537545, which is in linkage disequilibrium with interleukin-6 receptor polymorphism rs2228145. Further, individuals possessing at least one copy of the minor allele of either polymorphism expressed higher levels of soluble interleukin-6 receptor. These elevated interleukin-6 receptor levels may contribute to increased interleukin-6 activity through the trans-signaling pathway. These data suggest that interleukin-6 receptor polymorphism may be a contributing factor in Castleman Disease, and further research is warranted. Public Library of Science 2013-01-23 /pmc/articles/PMC3553080/ /pubmed/23372742 http://dx.doi.org/10.1371/journal.pone.0054610 Text en © 2013 Stone 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 Stone, Katie Woods, Emily Szmania, Susann M. Stephens, Owen W. Garg, Tarun K. Barlogie, Bart Shaughnessy, John D. Hall, Brett Reddy, Manjula Hoering, Antje Hansen, Emily van Rhee, Frits Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels |
title | Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels |
title_full | Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels |
title_fullStr | Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels |
title_full_unstemmed | Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels |
title_short | Interleukin-6 Receptor Polymorphism Is Prevalent in HIV-negative Castleman Disease and Is Associated with Increased Soluble Interleukin-6 Receptor Levels |
title_sort | interleukin-6 receptor polymorphism is prevalent in hiv-negative castleman disease and is associated with increased soluble interleukin-6 receptor levels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553080/ https://www.ncbi.nlm.nih.gov/pubmed/23372742 http://dx.doi.org/10.1371/journal.pone.0054610 |
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