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Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation

BACKGROUND: Breakdown of the gut mucosal barrier during chronic HIV infection allows translocation of bacterial products such as lipopolysaccharides (LPS) from the gut into the circulation. Microbial translocation also occurs in inflammatory bowel disease (IBD). IBD serological markers are useful in...

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Autores principales: Kamat, Anupa, Ancuta, Petronela, Blumberg, Richard S., Gabuzda, Dana
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2981579/
https://www.ncbi.nlm.nih.gov/pubmed/21125014
http://dx.doi.org/10.1371/journal.pone.0015533
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author Kamat, Anupa
Ancuta, Petronela
Blumberg, Richard S.
Gabuzda, Dana
author_facet Kamat, Anupa
Ancuta, Petronela
Blumberg, Richard S.
Gabuzda, Dana
author_sort Kamat, Anupa
collection PubMed
description BACKGROUND: Breakdown of the gut mucosal barrier during chronic HIV infection allows translocation of bacterial products such as lipopolysaccharides (LPS) from the gut into the circulation. Microbial translocation also occurs in inflammatory bowel disease (IBD). IBD serological markers are useful in the diagnosis of IBD and to differentiate between Crohn's disease (CD) and ulcerative colitis (UC). Here, we evaluate detection of IBD serological markers in HIV-infected patients with advanced disease and their relationship to HIV disease markers. METHODS: IBD serological markers (ASCA, pANCA, anti-OmpC, and anti-CBir1) were measured by ELISA in plasma from AIDS patients (n = 26) with low CD4 counts (<300 cells/µl) and high plasma LPS levels, and results correlated with clinical data. For meta-analysis, relevant data were abstracted from 20 articles. RESULTS: IBD serological markers were detected in approximately 65% of AIDS patients with evidence of microbial translocation. An antibody pattern consistent with IBD was detected in 46%; of these, 75% had a CD-like pattern. Meta-analysis of data from 20 published studies on IBD serological markers in CD, UC, and non-IBD control subjects indicated that IBD serological markers are detected more frequently in AIDS patients than in non-IBD disease controls and healthy controls, but less frequently than in CD patients. There was no association between IBD serological markers and HIV disease markers (plasma viral load and CD4 counts) in the study cohort. CONCLUSIONS: IBD serological markers may provide a non-invasive approach to monitor HIV-related inflammatory gut disease. Further studies to investigate their clinical significance in HIV-infected individuals are warranted.
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spelling pubmed-29815792010-12-01 Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation Kamat, Anupa Ancuta, Petronela Blumberg, Richard S. Gabuzda, Dana PLoS One Research Article BACKGROUND: Breakdown of the gut mucosal barrier during chronic HIV infection allows translocation of bacterial products such as lipopolysaccharides (LPS) from the gut into the circulation. Microbial translocation also occurs in inflammatory bowel disease (IBD). IBD serological markers are useful in the diagnosis of IBD and to differentiate between Crohn's disease (CD) and ulcerative colitis (UC). Here, we evaluate detection of IBD serological markers in HIV-infected patients with advanced disease and their relationship to HIV disease markers. METHODS: IBD serological markers (ASCA, pANCA, anti-OmpC, and anti-CBir1) were measured by ELISA in plasma from AIDS patients (n = 26) with low CD4 counts (<300 cells/µl) and high plasma LPS levels, and results correlated with clinical data. For meta-analysis, relevant data were abstracted from 20 articles. RESULTS: IBD serological markers were detected in approximately 65% of AIDS patients with evidence of microbial translocation. An antibody pattern consistent with IBD was detected in 46%; of these, 75% had a CD-like pattern. Meta-analysis of data from 20 published studies on IBD serological markers in CD, UC, and non-IBD control subjects indicated that IBD serological markers are detected more frequently in AIDS patients than in non-IBD disease controls and healthy controls, but less frequently than in CD patients. There was no association between IBD serological markers and HIV disease markers (plasma viral load and CD4 counts) in the study cohort. CONCLUSIONS: IBD serological markers may provide a non-invasive approach to monitor HIV-related inflammatory gut disease. Further studies to investigate their clinical significance in HIV-infected individuals are warranted. Public Library of Science 2010-11-15 /pmc/articles/PMC2981579/ /pubmed/21125014 http://dx.doi.org/10.1371/journal.pone.0015533 Text en Kamat 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
Kamat, Anupa
Ancuta, Petronela
Blumberg, Richard S.
Gabuzda, Dana
Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation
title Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation
title_full Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation
title_fullStr Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation
title_full_unstemmed Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation
title_short Serological Markers for Inflammatory Bowel Disease in AIDS Patients with Evidence of Microbial Translocation
title_sort serological markers for inflammatory bowel disease in aids patients with evidence of microbial translocation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2981579/
https://www.ncbi.nlm.nih.gov/pubmed/21125014
http://dx.doi.org/10.1371/journal.pone.0015533
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