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Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition

BACKGROUND: Familial Mediterranean fever (FMF) is an autoinflammatory condition, which is characterized by acute, self-limiting episodes of fever and serositis and chronic subclinical inflammation in remission. Here we investigated the consequence of this condition on the level of systemic antibodie...

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Autores principales: Manukyan, Gayane P., Ghazaryan, Karine A., Ktsoyan, Zhanna A., Khachatryan, Zaruhi A., Arakelova, Karine A., Kelly, Denise, Grant, George, Aminov, Rustam I.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525839/
https://www.ncbi.nlm.nih.gov/pubmed/18779861
http://dx.doi.org/10.1371/journal.pone.0003172
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author Manukyan, Gayane P.
Ghazaryan, Karine A.
Ktsoyan, Zhanna A.
Khachatryan, Zaruhi A.
Arakelova, Karine A.
Kelly, Denise
Grant, George
Aminov, Rustam I.
author_facet Manukyan, Gayane P.
Ghazaryan, Karine A.
Ktsoyan, Zhanna A.
Khachatryan, Zaruhi A.
Arakelova, Karine A.
Kelly, Denise
Grant, George
Aminov, Rustam I.
author_sort Manukyan, Gayane P.
collection PubMed
description BACKGROUND: Familial Mediterranean fever (FMF) is an autoinflammatory condition, which is characterized by acute, self-limiting episodes of fever and serositis and chronic subclinical inflammation in remission. Here we investigated the consequence of this condition on the level of systemic antibodies directed towards common intestinal bacteria. METHODOLOGY/PRINCIPAL FINDINGS: The level of systemic antibodies towards the antigens of Bacteroides, Parabacteroides, Escherichia, Enteroccocus and Lactobaccilus was measured by ELISA in FMF patients at various stages of the disease and in healthy controls. The difference between remission and attack was not significant. IgG antibodies against the antigens of Bacteroides, Parabacteroides, Escherichia and Enteroccocus were significantly increased in FMF compared to control while IgA levels were not significantly affected. Western blot analyses demonstrated the IgG reactivity against multiple antigens of commensal bacteria in FMF. Serological expression cloning was performed to identify these antigens. No single dominant antigen was identified; the response was generalized and directed against a variety of proteins from Bacteroides, Parabacteroides, Escherichia, and other gut commensals. CONCLUSIONS/SIGNIFICANCE: This autoinflammatory syndrome is characterized by the increased systemic reactivity against commensal gut microbiota. This is probably the consequence of hypersensitivity of the inflammasome in FMF that triggers the inflammation and contributes to the excessive translocation of bacteria and bacterial antigens through the gut barrier.
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spelling pubmed-25258392008-09-09 Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition Manukyan, Gayane P. Ghazaryan, Karine A. Ktsoyan, Zhanna A. Khachatryan, Zaruhi A. Arakelova, Karine A. Kelly, Denise Grant, George Aminov, Rustam I. PLoS One Research Article BACKGROUND: Familial Mediterranean fever (FMF) is an autoinflammatory condition, which is characterized by acute, self-limiting episodes of fever and serositis and chronic subclinical inflammation in remission. Here we investigated the consequence of this condition on the level of systemic antibodies directed towards common intestinal bacteria. METHODOLOGY/PRINCIPAL FINDINGS: The level of systemic antibodies towards the antigens of Bacteroides, Parabacteroides, Escherichia, Enteroccocus and Lactobaccilus was measured by ELISA in FMF patients at various stages of the disease and in healthy controls. The difference between remission and attack was not significant. IgG antibodies against the antigens of Bacteroides, Parabacteroides, Escherichia and Enteroccocus were significantly increased in FMF compared to control while IgA levels were not significantly affected. Western blot analyses demonstrated the IgG reactivity against multiple antigens of commensal bacteria in FMF. Serological expression cloning was performed to identify these antigens. No single dominant antigen was identified; the response was generalized and directed against a variety of proteins from Bacteroides, Parabacteroides, Escherichia, and other gut commensals. CONCLUSIONS/SIGNIFICANCE: This autoinflammatory syndrome is characterized by the increased systemic reactivity against commensal gut microbiota. This is probably the consequence of hypersensitivity of the inflammasome in FMF that triggers the inflammation and contributes to the excessive translocation of bacteria and bacterial antigens through the gut barrier. Public Library of Science 2008-09-09 /pmc/articles/PMC2525839/ /pubmed/18779861 http://dx.doi.org/10.1371/journal.pone.0003172 Text en Manukyan 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
Manukyan, Gayane P.
Ghazaryan, Karine A.
Ktsoyan, Zhanna A.
Khachatryan, Zaruhi A.
Arakelova, Karine A.
Kelly, Denise
Grant, George
Aminov, Rustam I.
Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition
title Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition
title_full Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition
title_fullStr Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition
title_full_unstemmed Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition
title_short Elevated Systemic Antibodies towards Commensal Gut Microbiota in Autoinflammatory Condition
title_sort elevated systemic antibodies towards commensal gut microbiota in autoinflammatory condition
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525839/
https://www.ncbi.nlm.nih.gov/pubmed/18779861
http://dx.doi.org/10.1371/journal.pone.0003172
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