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Shining a Light on Intestinal Traffic
Inflammatory bowel disease (IBD), encompassing Crohn's disease and ulcerative colitis, is associated with enhanced leukocyte infiltration to the gut, which is directly linked to the clinical aspects of these disorders. Thus, leukocyte trafficking is a major target for IBD therapy. Past and emer...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227234/ https://www.ncbi.nlm.nih.gov/pubmed/22162719 http://dx.doi.org/10.1155/2012/808157 |
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author | Murphy, Carola T. Nally, Kenneth Shanahan, Fergus Melgar, Silvia |
author_facet | Murphy, Carola T. Nally, Kenneth Shanahan, Fergus Melgar, Silvia |
author_sort | Murphy, Carola T. |
collection | PubMed |
description | Inflammatory bowel disease (IBD), encompassing Crohn's disease and ulcerative colitis, is associated with enhanced leukocyte infiltration to the gut, which is directly linked to the clinical aspects of these disorders. Thus, leukocyte trafficking is a major target for IBD therapy. Past and emerging techniques to study leukocyte trafficking both in vitro and in vivo have expanded our knowledge of the leukocyte migration process and the role of inhibitors. Various strategies have been employed to target chemokine- and integrin-ligand interactions within the multistep adhesion cascade and the S1P/S1PR1 axis in leukocyte migration. Though there is an abundance of preclinical data demonstrating efficacy of leukocyte trafficking inhibitors, many have yet to be confirmed in clinical studies. Vigilance for toxicity and further research is required into this complex and emerging area of IBD therapy. |
format | Online Article Text |
id | pubmed-3227234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32272342011-12-08 Shining a Light on Intestinal Traffic Murphy, Carola T. Nally, Kenneth Shanahan, Fergus Melgar, Silvia Clin Dev Immunol Review Article Inflammatory bowel disease (IBD), encompassing Crohn's disease and ulcerative colitis, is associated with enhanced leukocyte infiltration to the gut, which is directly linked to the clinical aspects of these disorders. Thus, leukocyte trafficking is a major target for IBD therapy. Past and emerging techniques to study leukocyte trafficking both in vitro and in vivo have expanded our knowledge of the leukocyte migration process and the role of inhibitors. Various strategies have been employed to target chemokine- and integrin-ligand interactions within the multistep adhesion cascade and the S1P/S1PR1 axis in leukocyte migration. Though there is an abundance of preclinical data demonstrating efficacy of leukocyte trafficking inhibitors, many have yet to be confirmed in clinical studies. Vigilance for toxicity and further research is required into this complex and emerging area of IBD therapy. Hindawi Publishing Corporation 2012 2011-11-22 /pmc/articles/PMC3227234/ /pubmed/22162719 http://dx.doi.org/10.1155/2012/808157 Text en Copyright © 2012 Carola T. Murphy et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Murphy, Carola T. Nally, Kenneth Shanahan, Fergus Melgar, Silvia Shining a Light on Intestinal Traffic |
title | Shining a Light on Intestinal Traffic |
title_full | Shining a Light on Intestinal Traffic |
title_fullStr | Shining a Light on Intestinal Traffic |
title_full_unstemmed | Shining a Light on Intestinal Traffic |
title_short | Shining a Light on Intestinal Traffic |
title_sort | shining a light on intestinal traffic |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227234/ https://www.ncbi.nlm.nih.gov/pubmed/22162719 http://dx.doi.org/10.1155/2012/808157 |
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