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ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease
BACKGROUND: Recently we reported IgA anti-Chlamydia antibodies in patients with Crohn’s disease (CD), in particular in four patients from a single family of six with CD. METHODS: We studied sera from four cohorts from the north of France. These were identified as: EPIMAD (80 pediatric onset CD and 2...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755634/ https://www.ncbi.nlm.nih.gov/pubmed/29317940 http://dx.doi.org/10.14740/gr922w |
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author | Van Kruiningen, Herbert J. Helal, Zeinab Leroyer, Ariane Garmendia, Antonio Gower-Rousseau, Corrine |
author_facet | Van Kruiningen, Herbert J. Helal, Zeinab Leroyer, Ariane Garmendia, Antonio Gower-Rousseau, Corrine |
author_sort | Van Kruiningen, Herbert J. |
collection | PubMed |
description | BACKGROUND: Recently we reported IgA anti-Chlamydia antibodies in patients with Crohn’s disease (CD), in particular in four patients from a single family of six with CD. METHODS: We studied sera from four cohorts from the north of France. These were identified as: EPIMAD (80 pediatric onset CD and 20 pediatric onset ulcerative colitis), MINOTOR (148 adult onset sporadic CD and 50 adult onset ulcerative colitis), Grande Famillies (50) and matched controls for the Grande Famillies cohort (49). Sera were tested using commercial anti-Chlamydia trachomatis (LGV2:434) IgG and IgA human enzyme-linked immunosorbent assay (ELISA) kits. Cutoff for positivity was 11.0 standard units. RESULTS: Patients with sporadic CD, unaffected first degree relatives from multiplex families and ulcerative colitis patients had no greater serologic reactivity than controls. However, multiplex families’ patients had twice as many positives as the other groups: for IgG 20% vs. 8%; for IgA 20% vs. 10%. CONCLUSIONS: Though not attaining statistical significance, the data showed that familial CD patients had greater exposure to C. trachomatis than sporadic CD patients, supporting our earlier results from one family from the north of France. More specific serologic tests based on outer membrane proteins will need to be employed against the various Chlamydia species with zoonotic potential. |
format | Online Article Text |
id | pubmed-5755634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57556342018-01-09 ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease Van Kruiningen, Herbert J. Helal, Zeinab Leroyer, Ariane Garmendia, Antonio Gower-Rousseau, Corrine Gastroenterology Res Original Article BACKGROUND: Recently we reported IgA anti-Chlamydia antibodies in patients with Crohn’s disease (CD), in particular in four patients from a single family of six with CD. METHODS: We studied sera from four cohorts from the north of France. These were identified as: EPIMAD (80 pediatric onset CD and 20 pediatric onset ulcerative colitis), MINOTOR (148 adult onset sporadic CD and 50 adult onset ulcerative colitis), Grande Famillies (50) and matched controls for the Grande Famillies cohort (49). Sera were tested using commercial anti-Chlamydia trachomatis (LGV2:434) IgG and IgA human enzyme-linked immunosorbent assay (ELISA) kits. Cutoff for positivity was 11.0 standard units. RESULTS: Patients with sporadic CD, unaffected first degree relatives from multiplex families and ulcerative colitis patients had no greater serologic reactivity than controls. However, multiplex families’ patients had twice as many positives as the other groups: for IgG 20% vs. 8%; for IgA 20% vs. 10%. CONCLUSIONS: Though not attaining statistical significance, the data showed that familial CD patients had greater exposure to C. trachomatis than sporadic CD patients, supporting our earlier results from one family from the north of France. More specific serologic tests based on outer membrane proteins will need to be employed against the various Chlamydia species with zoonotic potential. Elmer Press 2017-12 2018-01-03 /pmc/articles/PMC5755634/ /pubmed/29317940 http://dx.doi.org/10.14740/gr922w Text en Copyright 2017, Van Kruiningen et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Van Kruiningen, Herbert J. Helal, Zeinab Leroyer, Ariane Garmendia, Antonio Gower-Rousseau, Corrine ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease |
title | ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease |
title_full | ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease |
title_fullStr | ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease |
title_full_unstemmed | ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease |
title_short | ELISA Serology for Antibodies Against Chlamydia trachomatis in Crohn’s Disease |
title_sort | elisa serology for antibodies against chlamydia trachomatis in crohn’s disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755634/ https://www.ncbi.nlm.nih.gov/pubmed/29317940 http://dx.doi.org/10.14740/gr922w |
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