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Regulatory T Cell Subsets in Filarial Infection and Their Function

Identifieur interne : 004994 ( Pmc/Curation ); précédent : 004993; suivant : 004995

Regulatory T Cell Subsets in Filarial Infection and Their Function

Auteurs : Simon Metenou [États-Unis] ; Thomas B. Nutman [États-Unis]

Source :

RBID : PMC:3786323

Abstract

Filarial infections in humans are chronic infections that cause significant morbidity. The chronic nature of these infections with continuous antigen release is associated with a parasite-specific T cell hypo-responsiveness that may over time also affect the immune responses to bystander antigens. Previous studies have shown the filarial parasite antigen-specific T cells hypo-responsiveness is mediated by regulatory cytokines – IL-10 and TGF-β in particular. Recent studies have suggested that the modulated/regulated T cell responses associated with patent filarial infection may reflect an expansion of regulatory T cells (Tregs) that include both Tregs induced in peripheral circulation or pTregs and the thymus-derived Tregs or tTregs. Although much is known about the phenotype of these regulatory populations, the mechanisms underlying their expansion and their mode of action in filarial and other infections remain unclear. Nevertheless there are data to suggest that while many of these regulatory cells are activated in an antigen-specific manner the ensuing effectors of this activation are relatively non-specific and may affect a broad range of immune cells. This review will focus on the subsets and function of regulatory T cells in filarial infection.


Url:
DOI: 10.3389/fimmu.2013.00305
PubMed: 24137161
PubMed Central: 3786323

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PMC:3786323

Le document en format XML

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<p>Filarial infections in humans are chronic infections that cause significant morbidity. The chronic nature of these infections with continuous antigen release is associated with a parasite-specific T cell hypo-responsiveness that may over time also affect the immune responses to bystander antigens. Previous studies have shown the filarial parasite antigen-specific T cells hypo-responsiveness is mediated by regulatory cytokines – IL-10 and TGF-β in particular. Recent studies have suggested that the modulated/regulated T cell responses associated with patent filarial infection may reflect an expansion of regulatory T cells (Tregs) that include both Tregs induced in peripheral circulation or pTregs and the thymus-derived Tregs or tTregs. Although much is known about the phenotype of these regulatory populations, the mechanisms underlying their expansion and their mode of action in filarial and other infections remain unclear. Nevertheless there are data to suggest that while many of these regulatory cells are activated in an antigen-specific manner the ensuing effectors of this activation are relatively non-specific and may affect a broad range of immune cells. This review will focus on the subsets and function of regulatory T cells in filarial infection.</p>
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<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Front Immunol</journal-id>
<journal-id journal-id-type="iso-abbrev">Front Immunol</journal-id>
<journal-id journal-id-type="publisher-id">Front. Immunol.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Immunology</journal-title>
</journal-title-group>
<issn pub-type="epub">1664-3224</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">24137161</article-id>
<article-id pub-id-type="pmc">3786323</article-id>
<article-id pub-id-type="doi">10.3389/fimmu.2013.00305</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Immunology</subject>
<subj-group>
<subject>Review Article</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Regulatory T Cell Subsets in Filarial Infection and Their Function</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Metenou</surname>
<given-names>Simon</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nutman</surname>
<given-names>Thomas B.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="cor1">*</xref>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Helminth Immunology Section, Laboratory of Parasitic Diseases, National Institutes of Health</institution>
,
<addr-line>Bethesda, MD</addr-line>
,
<country>USA</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Eyad Elkord, United Arab Emirates University, UAE; University of Salford and University of Manchester, UK</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Rick M. Maizels, The University of Edinburgh, UK; Matthew Taylor, The University of Edinburgh, UK</p>
</fn>
<corresp content-type="corresp" id="cor1">*Correspondence: Thomas B. Nutman, Helminth Immunology Section, Laboratory of Parasitic Diseases, National Institutes of Health, 4 Center Dr. Building 4 Room B1-03, Bethesda, MD 20892, USA e-mail:
<email>tnutman@naiaid.nih.gov</email>
</corresp>
<fn fn-type="other" id="fn001">
<p>This article was submitted to Immunological Tolerance, a section of the journal Frontiers in Immunology.</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>30</day>
<month>9</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="collection">
<year>2013</year>
</pub-date>
<volume>4</volume>
<elocation-id>305</elocation-id>
<history>
<date date-type="received">
<day>31</day>
<month>5</month>
<year>2013</year>
</date>
<date date-type="accepted">
<day>13</day>
<month>9</month>
<year>2013</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2013 Metenou and Nutman.</copyright-statement>
<copyright-year>2013</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/3.0/">
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<p>Filarial infections in humans are chronic infections that cause significant morbidity. The chronic nature of these infections with continuous antigen release is associated with a parasite-specific T cell hypo-responsiveness that may over time also affect the immune responses to bystander antigens. Previous studies have shown the filarial parasite antigen-specific T cells hypo-responsiveness is mediated by regulatory cytokines – IL-10 and TGF-β in particular. Recent studies have suggested that the modulated/regulated T cell responses associated with patent filarial infection may reflect an expansion of regulatory T cells (Tregs) that include both Tregs induced in peripheral circulation or pTregs and the thymus-derived Tregs or tTregs. Although much is known about the phenotype of these regulatory populations, the mechanisms underlying their expansion and their mode of action in filarial and other infections remain unclear. Nevertheless there are data to suggest that while many of these regulatory cells are activated in an antigen-specific manner the ensuing effectors of this activation are relatively non-specific and may affect a broad range of immune cells. This review will focus on the subsets and function of regulatory T cells in filarial infection.</p>
</abstract>
<kwd-group>
<kwd>tTregs</kwd>
<kwd>pTregs</kwd>
<kwd>Tr1</kwd>
<kwd>Th3</kwd>
<kwd>filarial infection</kwd>
<kwd>
<italic>O. volvulus</italic>
</kwd>
<kwd>
<italic>W. bancrofti</italic>
</kwd>
<kwd>
<italic>B. malayi</italic>
</kwd>
</kwd-group>
<counts>
<fig-count count="1"></fig-count>
<table-count count="0"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="141"></ref-count>
<page-count count="8"></page-count>
<word-count count="7818"></word-count>
</counts>
</article-meta>
</front>
</pmc>
</record>

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