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Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection
The mucosal cytokine response of healthy humans to parasitic helminths has never been reported. We investigated the systemic and mucosal cytokine responses to hookworm infection in experimentally infected, previously hookworm naive individuals from non-endemic areas. We collected both peripheral blo...
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/PMC3276555/ https://www.ncbi.nlm.nih.gov/pubmed/22346753 http://dx.doi.org/10.1371/journal.ppat.1002520 |
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author | Gaze, Soraya McSorley, Henry J. Daveson, James Jones, Di Bethony, Jeffrey M. Oliveira, Luciana M. Speare, Richard McCarthy, James S. Engwerda, Christian R. Croese, John Loukas, Alex |
author_facet | Gaze, Soraya McSorley, Henry J. Daveson, James Jones, Di Bethony, Jeffrey M. Oliveira, Luciana M. Speare, Richard McCarthy, James S. Engwerda, Christian R. Croese, John Loukas, Alex |
author_sort | Gaze, Soraya |
collection | PubMed |
description | The mucosal cytokine response of healthy humans to parasitic helminths has never been reported. We investigated the systemic and mucosal cytokine responses to hookworm infection in experimentally infected, previously hookworm naive individuals from non-endemic areas. We collected both peripheral blood and duodenal biopsies to assess the systemic immune response, as well as the response at the site of adult worm establishment. Our results show that experimental hookworm infection leads to a strong systemic and mucosal Th2 (IL-4, IL-5, IL-9 and IL-13) and regulatory (IL-10 and TGF-β) response, with some evidence of a Th1 (IFN-γ and IL-2) response. Despite upregulation after patency of both IL-15 and ALDH1A2, a known Th17-inducing combination in inflammatory diseases, we saw no evidence of a Th17 (IL-17) response. Moreover, we observed strong suppression of mucosal IL-23 and upregulation of IL-22 during established hookworm infection, suggesting a potential mechanism by which Th17 responses are suppressed, and highlighting the potential that hookworms and their secreted proteins offer as therapeutics for human inflammatory diseases. |
format | Online Article Text |
id | pubmed-3276555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32765552012-02-15 Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection Gaze, Soraya McSorley, Henry J. Daveson, James Jones, Di Bethony, Jeffrey M. Oliveira, Luciana M. Speare, Richard McCarthy, James S. Engwerda, Christian R. Croese, John Loukas, Alex PLoS Pathog Research Article The mucosal cytokine response of healthy humans to parasitic helminths has never been reported. We investigated the systemic and mucosal cytokine responses to hookworm infection in experimentally infected, previously hookworm naive individuals from non-endemic areas. We collected both peripheral blood and duodenal biopsies to assess the systemic immune response, as well as the response at the site of adult worm establishment. Our results show that experimental hookworm infection leads to a strong systemic and mucosal Th2 (IL-4, IL-5, IL-9 and IL-13) and regulatory (IL-10 and TGF-β) response, with some evidence of a Th1 (IFN-γ and IL-2) response. Despite upregulation after patency of both IL-15 and ALDH1A2, a known Th17-inducing combination in inflammatory diseases, we saw no evidence of a Th17 (IL-17) response. Moreover, we observed strong suppression of mucosal IL-23 and upregulation of IL-22 during established hookworm infection, suggesting a potential mechanism by which Th17 responses are suppressed, and highlighting the potential that hookworms and their secreted proteins offer as therapeutics for human inflammatory diseases. Public Library of Science 2012-02-09 /pmc/articles/PMC3276555/ /pubmed/22346753 http://dx.doi.org/10.1371/journal.ppat.1002520 Text en Gaze 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 Gaze, Soraya McSorley, Henry J. Daveson, James Jones, Di Bethony, Jeffrey M. Oliveira, Luciana M. Speare, Richard McCarthy, James S. Engwerda, Christian R. Croese, John Loukas, Alex Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection |
title | Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection |
title_full | Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection |
title_fullStr | Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection |
title_full_unstemmed | Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection |
title_short | Characterising the Mucosal and Systemic Immune Responses to Experimental Human Hookworm Infection |
title_sort | characterising the mucosal and systemic immune responses to experimental human hookworm infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276555/ https://www.ncbi.nlm.nih.gov/pubmed/22346753 http://dx.doi.org/10.1371/journal.ppat.1002520 |
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