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Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice
Gluten sensitivity may affect disease pathogenesis in a subset of individuals who have schizophrenia, bipolar disorder or autism. Exposure to Toxoplasma gondii is a known risk factor for the development of schizophrenia, presumably through a direct pathological effect of the parasite on brain and be...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510169/ https://www.ncbi.nlm.nih.gov/pubmed/23209841 http://dx.doi.org/10.1371/journal.pone.0050991 |
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author | Severance, Emily G. Kannan, Geetha Gressitt, Kristin L. Xiao, Jianchun Alaedini, Armin Pletnikov, Mikhail V. Yolken, Robert H. |
author_facet | Severance, Emily G. Kannan, Geetha Gressitt, Kristin L. Xiao, Jianchun Alaedini, Armin Pletnikov, Mikhail V. Yolken, Robert H. |
author_sort | Severance, Emily G. |
collection | PubMed |
description | Gluten sensitivity may affect disease pathogenesis in a subset of individuals who have schizophrenia, bipolar disorder or autism. Exposure to Toxoplasma gondii is a known risk factor for the development of schizophrenia, presumably through a direct pathological effect of the parasite on brain and behavior. A co-association of antibodies to wheat gluten and to T. gondii in individuals with schizophrenia was recently uncovered, suggesting a coordinated gastrointestinal means by which T. gondii and dietary gluten might generate an immune response. Here, we evaluated the connection between these infectious- and food-based antigens in mouse models. BALB/c mice receiving a standard wheat-based rodent chow were infected with T. gondii via intraperitoneal, peroral and prenatal exposure methods. Significant increases in the levels of anti-gluten IgG were documented in all infected mice and in offspring from chronically infected dams compared to uninfected controls (repetitive measures ANOVAs, two-tailed t-tests, all p≤0.00001). Activation of the complement system accompanied this immune response (p≤0.002–0.00001). Perorally-infected females showed higher levels of anti-gluten IgG than males (p≤0.009) indicating that T. gondii-generated gastrointestinal infection led to a significant anti-gluten immune response in a sex-dependent manner. These findings support a gastrointestinal basis by which two risk factors for schizophrenia, T. gondii infection and sensitivity to dietary gluten, might be connected to produce the immune activation that is becoming an increasingly recognized pathology of psychiatric disorders. |
format | Online Article Text |
id | pubmed-3510169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35101692012-12-03 Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice Severance, Emily G. Kannan, Geetha Gressitt, Kristin L. Xiao, Jianchun Alaedini, Armin Pletnikov, Mikhail V. Yolken, Robert H. PLoS One Research Article Gluten sensitivity may affect disease pathogenesis in a subset of individuals who have schizophrenia, bipolar disorder or autism. Exposure to Toxoplasma gondii is a known risk factor for the development of schizophrenia, presumably through a direct pathological effect of the parasite on brain and behavior. A co-association of antibodies to wheat gluten and to T. gondii in individuals with schizophrenia was recently uncovered, suggesting a coordinated gastrointestinal means by which T. gondii and dietary gluten might generate an immune response. Here, we evaluated the connection between these infectious- and food-based antigens in mouse models. BALB/c mice receiving a standard wheat-based rodent chow were infected with T. gondii via intraperitoneal, peroral and prenatal exposure methods. Significant increases in the levels of anti-gluten IgG were documented in all infected mice and in offspring from chronically infected dams compared to uninfected controls (repetitive measures ANOVAs, two-tailed t-tests, all p≤0.00001). Activation of the complement system accompanied this immune response (p≤0.002–0.00001). Perorally-infected females showed higher levels of anti-gluten IgG than males (p≤0.009) indicating that T. gondii-generated gastrointestinal infection led to a significant anti-gluten immune response in a sex-dependent manner. These findings support a gastrointestinal basis by which two risk factors for schizophrenia, T. gondii infection and sensitivity to dietary gluten, might be connected to produce the immune activation that is becoming an increasingly recognized pathology of psychiatric disorders. Public Library of Science 2012-11-29 /pmc/articles/PMC3510169/ /pubmed/23209841 http://dx.doi.org/10.1371/journal.pone.0050991 Text en © 2012 Severance 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 Severance, Emily G. Kannan, Geetha Gressitt, Kristin L. Xiao, Jianchun Alaedini, Armin Pletnikov, Mikhail V. Yolken, Robert H. Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice |
title | Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice |
title_full | Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice |
title_fullStr | Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice |
title_full_unstemmed | Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice |
title_short | Anti-Gluten Immune Response following Toxoplasma gondii Infection in Mice |
title_sort | anti-gluten immune response following toxoplasma gondii infection in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510169/ https://www.ncbi.nlm.nih.gov/pubmed/23209841 http://dx.doi.org/10.1371/journal.pone.0050991 |
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