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Pro-inflammatory cytokines in cryptoglandular anal fistulas
BACKGROUND: Sphincter-preserving procedures for the treatment of transsphincteric fistulas fail in at least one out of every three patients. It has been suggested that failure is due to ongoing disease in the remaining fistula tract. Cytokines play an important role in inflammation. At present, biol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003909/ https://www.ncbi.nlm.nih.gov/pubmed/27402195 http://dx.doi.org/10.1007/s10151-016-1494-7 |
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author | van Onkelen, R. S. Gosselink, M. P. van Meurs, M. Melief, M. J. Schouten, W. R. Laman, J. D. |
author_facet | van Onkelen, R. S. Gosselink, M. P. van Meurs, M. Melief, M. J. Schouten, W. R. Laman, J. D. |
author_sort | van Onkelen, R. S. |
collection | PubMed |
description | BACKGROUND: Sphincter-preserving procedures for the treatment of transsphincteric fistulas fail in at least one out of every three patients. It has been suggested that failure is due to ongoing disease in the remaining fistula tract. Cytokines play an important role in inflammation. At present, biologicals targeting cytokines are available. Therefore, detection and identification of cytokines in anal fistulas might have implications for future treatment modalities. The objective of the present study was to assess local production of a selected panel of cytokines in anal fistulas, including pro-inflammatory interleukin (IL)-1β and tumor necrosis factor α (TNF-α). METHODS: Fistula tract tissue was obtained from 27 patients with a transsphincteric fistula of cryptoglandular origin who underwent flap repair, ligation of the intersphincteric fistula tract or a combination of both procedures. Patients with a rectovaginal fistula or a fistula due to Crohn’s disease were excluded. Frozen tissue samples were sectioned and stained using advanced immuno-enzyme staining methods for detection of selected cytokines, IL-1β, IL-8, IL-10, IL-12p40, IL-17A, IL-18, IL-36 and TNF-α. The presence and frequencies of cytokine-producing cells in samples were quantitated. RESULTS: The key finding was abundant expression of IL-1β in 93 % of the anal fistulas. Frequencies of IL-1β-producing cells were highest (>50 positive stained cells) in 7 % of the anal fistulas. Also, cytokines IL-8, IL-12p40 and TNF-α were present in respectively 70, 33 and 30 % of the anal fistulas. CONCLUSIONS: IL-1β is expressed in the large majority of cryptoglandular anal fistulas, as well as several other pro-inflammatory cytokines. |
format | Online Article Text |
id | pubmed-5003909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-50039092016-09-15 Pro-inflammatory cytokines in cryptoglandular anal fistulas van Onkelen, R. S. Gosselink, M. P. van Meurs, M. Melief, M. J. Schouten, W. R. Laman, J. D. Tech Coloproctol Original Article BACKGROUND: Sphincter-preserving procedures for the treatment of transsphincteric fistulas fail in at least one out of every three patients. It has been suggested that failure is due to ongoing disease in the remaining fistula tract. Cytokines play an important role in inflammation. At present, biologicals targeting cytokines are available. Therefore, detection and identification of cytokines in anal fistulas might have implications for future treatment modalities. The objective of the present study was to assess local production of a selected panel of cytokines in anal fistulas, including pro-inflammatory interleukin (IL)-1β and tumor necrosis factor α (TNF-α). METHODS: Fistula tract tissue was obtained from 27 patients with a transsphincteric fistula of cryptoglandular origin who underwent flap repair, ligation of the intersphincteric fistula tract or a combination of both procedures. Patients with a rectovaginal fistula or a fistula due to Crohn’s disease were excluded. Frozen tissue samples were sectioned and stained using advanced immuno-enzyme staining methods for detection of selected cytokines, IL-1β, IL-8, IL-10, IL-12p40, IL-17A, IL-18, IL-36 and TNF-α. The presence and frequencies of cytokine-producing cells in samples were quantitated. RESULTS: The key finding was abundant expression of IL-1β in 93 % of the anal fistulas. Frequencies of IL-1β-producing cells were highest (>50 positive stained cells) in 7 % of the anal fistulas. Also, cytokines IL-8, IL-12p40 and TNF-α were present in respectively 70, 33 and 30 % of the anal fistulas. CONCLUSIONS: IL-1β is expressed in the large majority of cryptoglandular anal fistulas, as well as several other pro-inflammatory cytokines. Springer International Publishing 2016-07-11 2016 /pmc/articles/PMC5003909/ /pubmed/27402195 http://dx.doi.org/10.1007/s10151-016-1494-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article van Onkelen, R. S. Gosselink, M. P. van Meurs, M. Melief, M. J. Schouten, W. R. Laman, J. D. Pro-inflammatory cytokines in cryptoglandular anal fistulas |
title | Pro-inflammatory cytokines in cryptoglandular anal fistulas |
title_full | Pro-inflammatory cytokines in cryptoglandular anal fistulas |
title_fullStr | Pro-inflammatory cytokines in cryptoglandular anal fistulas |
title_full_unstemmed | Pro-inflammatory cytokines in cryptoglandular anal fistulas |
title_short | Pro-inflammatory cytokines in cryptoglandular anal fistulas |
title_sort | pro-inflammatory cytokines in cryptoglandular anal fistulas |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003909/ https://www.ncbi.nlm.nih.gov/pubmed/27402195 http://dx.doi.org/10.1007/s10151-016-1494-7 |
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