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A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease
Ectromelia virus (ECTV) is an orthopoxvirus (OPV) that causes mousepox, the murine equivalent of human smallpox. C57BL/6 (B6) mice are naturally resistant to mousepox due to the concerted action of innate and adaptive immune responses. Previous studies have shown that natural killer (NK) cells are a...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233669/ https://www.ncbi.nlm.nih.gov/pubmed/18266471 http://dx.doi.org/10.1371/journal.ppat.0040030 |
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author | Fang, Min Lanier, Lewis L Sigal, Luis J |
author_facet | Fang, Min Lanier, Lewis L Sigal, Luis J |
author_sort | Fang, Min |
collection | PubMed |
description | Ectromelia virus (ECTV) is an orthopoxvirus (OPV) that causes mousepox, the murine equivalent of human smallpox. C57BL/6 (B6) mice are naturally resistant to mousepox due to the concerted action of innate and adaptive immune responses. Previous studies have shown that natural killer (NK) cells are a component of innate immunity that is essential for the B6 mice resistance to mousepox. However, the mechanism of NK cell–mediated resistance to OPV disease remains undefined. Here we show that B6 mice resistance to mousepox requires the direct cytolytic function of NK cells, as well as their ability to boost the T cell response. Furthermore, we show that the activating receptor NKG2D is required for optimal NK cell–mediated resistance to disease and lethality. Together, our results have important implication towards the understanding of natural resistance to pathogenic viral infections. |
format | Text |
id | pubmed-2233669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22336692008-02-08 A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease Fang, Min Lanier, Lewis L Sigal, Luis J PLoS Pathog Research Article Ectromelia virus (ECTV) is an orthopoxvirus (OPV) that causes mousepox, the murine equivalent of human smallpox. C57BL/6 (B6) mice are naturally resistant to mousepox due to the concerted action of innate and adaptive immune responses. Previous studies have shown that natural killer (NK) cells are a component of innate immunity that is essential for the B6 mice resistance to mousepox. However, the mechanism of NK cell–mediated resistance to OPV disease remains undefined. Here we show that B6 mice resistance to mousepox requires the direct cytolytic function of NK cells, as well as their ability to boost the T cell response. Furthermore, we show that the activating receptor NKG2D is required for optimal NK cell–mediated resistance to disease and lethality. Together, our results have important implication towards the understanding of natural resistance to pathogenic viral infections. Public Library of Science 2008-02 2008-02-08 /pmc/articles/PMC2233669/ /pubmed/18266471 http://dx.doi.org/10.1371/journal.ppat.0040030 Text en © 2008 Fang 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 Fang, Min Lanier, Lewis L Sigal, Luis J A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease |
title | A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease |
title_full | A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease |
title_fullStr | A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease |
title_full_unstemmed | A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease |
title_short | A Role for NKG2D in NK Cell–Mediated Resistance to Poxvirus Disease |
title_sort | role for nkg2d in nk cell–mediated resistance to poxvirus disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233669/ https://www.ncbi.nlm.nih.gov/pubmed/18266471 http://dx.doi.org/10.1371/journal.ppat.0040030 |
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