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Critical role of IRF-5 in the development of T helper 1 responses to Leishmania donovani infection
The transcription factor Interferon Regulatory Factor 5 (IRF-5) has been shown to be involved in the induction of proinflammatory cytokines in response to viral infections and TLR activation and to play an essential role in the innate inflammatory response. In this study, we used the experimental mo...
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Published in: | PLoS pathogens 2011-01, Vol.7 (1), p.e1001246-e1001246 |
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description | The transcription factor Interferon Regulatory Factor 5 (IRF-5) has been shown to be involved in the induction of proinflammatory cytokines in response to viral infections and TLR activation and to play an essential role in the innate inflammatory response. In this study, we used the experimental model of visceral leishmaniasis to investigate the role of IRF-5 in the generation of Th1 responses and in the formation of Th1-type liver granulomas in Leishmania donovani infected mice. We show that TLR7-mediated activation of IRF-5 is essential for the development of Th1 responses to L. donovani in the spleen during chronic infection. We also demonstrate that IRF-5 deficiency leads to the incapacity to control L. donovani infection in the liver and to the formation of smaller granulomas. Granulomas in Irf5⁻/⁻ mice are characterized by an increased IL-4 and IL-10 response and concomitant low iNOS expression. Collectively, these results identify IRF-5 as a critical molecular switch for the development of Th1 immune responses following L. donovani infections and reveal an indirect role of IRF-5 in the regulation of iNOS expression. |
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Collectively, these results identify IRF-5 as a critical molecular switch for the development of Th1 immune responses following L. donovani infections and reveal an indirect role of IRF-5 in the regulation of iNOS expression.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1001246</identifier><identifier>PMID: 21253574</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Development and progression ; Disease Models, Animal ; Female ; Gene Expression ; Granuloma - immunology ; Granuloma - parasitology ; Granuloma - pathology ; HEK293 Cells - enzymology ; Host-Parasite Interactions ; Humans ; Immune response ; Immune system ; Immunology/Immune Response ; Immunology/Immunity to Infections ; Immunology/Innate Immunity ; Inbreeding ; Infections ; Infectious Diseases/Neglected Tropical Diseases ; Infectious Diseases/Protozoal Infections ; Interferon ; Interferon Regulatory Factors - deficiency ; Interferon Regulatory Factors - physiology ; Leishmania donovani ; Leishmania donovani - immunology ; Leishmaniasis, Cutaneous ; Leishmaniasis, Visceral - genetics ; Leishmaniasis, Visceral - immunology ; Leishmaniasis, Visceral - metabolism ; Liver - immunology ; Liver - parasitology ; Liver - pathology ; Luciferases - genetics ; Luciferases - metabolism ; Lymphocytes ; Macrophages - immunology ; Macrophages - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Nitric Oxide Synthase Type II - genetics ; Nitric Oxide Synthase Type II - metabolism ; Parasites ; Parasitic diseases ; Physiological aspects ; Proteins ; Regulation ; RNA, Messenger - metabolism ; Spleen - immunology ; Spleen - parasitology ; Spleen - pathology ; Th1 Cells - immunology ; Th1 Cells - metabolism ; Toll-like receptors ; Transfection ; Vector-borne diseases ; Viral infections</subject><ispartof>PLoS pathogens, 2011-01, Vol.7 (1), p.e1001246-e1001246</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Paun et al. 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 credited: Paun A, Bankoti R, Joshi T, Pitha PM, Stäger S (2011) Critical Role of IRF-5 in the Development of T helper 1 responses to Leishmania donovani infection. 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Collectively, these results identify IRF-5 as a critical molecular switch for the development of Th1 immune responses following L. donovani infections and reveal an indirect role of IRF-5 in the regulation of iNOS expression.</description><subject>Animals</subject><subject>Development and progression</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Granuloma - immunology</subject><subject>Granuloma - parasitology</subject><subject>Granuloma - pathology</subject><subject>HEK293 Cells - enzymology</subject><subject>Host-Parasite Interactions</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunology/Immune Response</subject><subject>Immunology/Immunity to Infections</subject><subject>Immunology/Innate Immunity</subject><subject>Inbreeding</subject><subject>Infections</subject><subject>Infectious Diseases/Neglected Tropical Diseases</subject><subject>Infectious Diseases/Protozoal Infections</subject><subject>Interferon</subject><subject>Interferon Regulatory Factors - deficiency</subject><subject>Interferon Regulatory Factors - physiology</subject><subject>Leishmania donovani</subject><subject>Leishmania donovani - immunology</subject><subject>Leishmaniasis, Cutaneous</subject><subject>Leishmaniasis, Visceral - genetics</subject><subject>Leishmaniasis, Visceral - immunology</subject><subject>Leishmaniasis, Visceral - metabolism</subject><subject>Liver - immunology</subject><subject>Liver - parasitology</subject><subject>Liver - pathology</subject><subject>Luciferases - genetics</subject><subject>Luciferases - metabolism</subject><subject>Lymphocytes</subject><subject>Macrophages - immunology</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Regulation</subject><subject>RNA, Messenger - metabolism</subject><subject>Spleen - immunology</subject><subject>Spleen - parasitology</subject><subject>Spleen - pathology</subject><subject>Th1 Cells - immunology</subject><subject>Th1 Cells - metabolism</subject><subject>Toll-like receptors</subject><subject>Transfection</subject><subject>Vector-borne diseases</subject><subject>Viral infections</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqVk12LEzEUhgdR3HX1H4gGvBAvWvM1M8mNsBRXC0VhXa9DJnPSpmQmYzIt-u9N7eyylQWRXCQkz3lz8p6conhJ8Jywmrzfhl3stZ8Pgx7nBGNCefWoOCdlyWY1q_nje-uz4llKW4w5YaR6WpxRQktW1vy8aBbRjc5oj2LwgIJFy-urWYlcj8YNoBb24MPQQT8ezm7QBvwAEREUIQ2hT5DQGNAKXNp0uncataEP-7zKChbM6EL_vHhitU_wYpoviu9XH28Wn2err5-Wi8vVzFSSjjMjREOhLNvaNmBKa4DWoq6gbIm1DISVhAFmjWwYbkgJjMmWGSqNZZaXDNhF8fqoO_iQ1GRPUoQKiaWQAmdieSTaoLdqiK7T8ZcK2qk_GyGulY7ZDQ9KE8mbSmCgUnIOVmBrrRR1Ixm3QvCs9WG6bdd00JrsUNT-RPT0pHcbtQ57xTCpCT0k83YSiOHHDtKoOpcMeK97CLukJMkZC5oL9S9S8EpihjnN5Ju_yIdtmKi1zi_NdQo5QXPQVJeUCy7z1xCZmj9A5dFC50zowbq8fxLw7iQgMyP8HNd6l5Jafrv-D_bLKcuPrIkhpQj2zmSC1aEVbh-pDq2gplbIYa_uF-gu6Pbvs9-w2gOR</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Paun, Andrea</creator><creator>Bankoti, Rashmi</creator><creator>Joshi, Trupti</creator><creator>Pitha, Paula M</creator><creator>Stäger, Simona</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>M7N</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110101</creationdate><title>Critical role of IRF-5 in the development of T helper 1 responses to Leishmania donovani infection</title><author>Paun, Andrea ; Bankoti, Rashmi ; Joshi, Trupti ; Pitha, Paula M ; Stäger, Simona</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-c88b2e55d7fbec5fce27876e5d1ff3e8f913e03b9b30b15e339d3c29cf3f453e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Development and progression</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Granuloma - immunology</topic><topic>Granuloma - parasitology</topic><topic>Granuloma - pathology</topic><topic>HEK293 Cells - enzymology</topic><topic>Host-Parasite Interactions</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunology/Immune Response</topic><topic>Immunology/Immunity to Infections</topic><topic>Immunology/Innate Immunity</topic><topic>Inbreeding</topic><topic>Infections</topic><topic>Infectious Diseases/Neglected Tropical Diseases</topic><topic>Infectious Diseases/Protozoal Infections</topic><topic>Interferon</topic><topic>Interferon Regulatory Factors - deficiency</topic><topic>Interferon Regulatory Factors - physiology</topic><topic>Leishmania donovani</topic><topic>Leishmania donovani - immunology</topic><topic>Leishmaniasis, Cutaneous</topic><topic>Leishmaniasis, Visceral - genetics</topic><topic>Leishmaniasis, Visceral - immunology</topic><topic>Leishmaniasis, Visceral - metabolism</topic><topic>Liver - immunology</topic><topic>Liver - parasitology</topic><topic>Liver - pathology</topic><topic>Luciferases - genetics</topic><topic>Luciferases - metabolism</topic><topic>Lymphocytes</topic><topic>Macrophages - immunology</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Nitric Oxide Synthase Type II - genetics</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Parasites</topic><topic>Parasitic diseases</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Regulation</topic><topic>RNA, Messenger - metabolism</topic><topic>Spleen - immunology</topic><topic>Spleen - parasitology</topic><topic>Spleen - pathology</topic><topic>Th1 Cells - immunology</topic><topic>Th1 Cells - metabolism</topic><topic>Toll-like receptors</topic><topic>Transfection</topic><topic>Vector-borne diseases</topic><topic>Viral infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paun, Andrea</creatorcontrib><creatorcontrib>Bankoti, Rashmi</creatorcontrib><creatorcontrib>Joshi, Trupti</creatorcontrib><creatorcontrib>Pitha, Paula M</creatorcontrib><creatorcontrib>Stäger, Simona</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paun, Andrea</au><au>Bankoti, Rashmi</au><au>Joshi, Trupti</au><au>Pitha, Paula M</au><au>Stäger, Simona</au><au>Müller, Ingrid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Critical role of IRF-5 in the development of T helper 1 responses to Leishmania donovani infection</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>7</volume><issue>1</issue><spage>e1001246</spage><epage>e1001246</epage><pages>e1001246-e1001246</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>The transcription factor Interferon Regulatory Factor 5 (IRF-5) has been shown to be involved in the induction of proinflammatory cytokines in response to viral infections and TLR activation and to play an essential role in the innate inflammatory response. In this study, we used the experimental model of visceral leishmaniasis to investigate the role of IRF-5 in the generation of Th1 responses and in the formation of Th1-type liver granulomas in Leishmania donovani infected mice. We show that TLR7-mediated activation of IRF-5 is essential for the development of Th1 responses to L. donovani in the spleen during chronic infection. We also demonstrate that IRF-5 deficiency leads to the incapacity to control L. donovani infection in the liver and to the formation of smaller granulomas. Granulomas in Irf5⁻/⁻ mice are characterized by an increased IL-4 and IL-10 response and concomitant low iNOS expression. Collectively, these results identify IRF-5 as a critical molecular switch for the development of Th1 immune responses following L. donovani infections and reveal an indirect role of IRF-5 in the regulation of iNOS expression.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21253574</pmid><doi>10.1371/journal.ppat.1001246</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Development and progression Disease Models, Animal Female Gene Expression Granuloma - immunology Granuloma - parasitology Granuloma - pathology HEK293 Cells - enzymology Host-Parasite Interactions Humans Immune response Immune system Immunology/Immune Response Immunology/Immunity to Infections Immunology/Innate Immunity Inbreeding Infections Infectious Diseases/Neglected Tropical Diseases Infectious Diseases/Protozoal Infections Interferon Interferon Regulatory Factors - deficiency Interferon Regulatory Factors - physiology Leishmania donovani Leishmania donovani - immunology Leishmaniasis, Cutaneous Leishmaniasis, Visceral - genetics Leishmaniasis, Visceral - immunology Leishmaniasis, Visceral - metabolism Liver - immunology Liver - parasitology Liver - pathology Luciferases - genetics Luciferases - metabolism Lymphocytes Macrophages - immunology Macrophages - metabolism Male Mice Mice, Inbred C57BL Mice, Knockout Nitric Oxide Synthase Type II - genetics Nitric Oxide Synthase Type II - metabolism Parasites Parasitic diseases Physiological aspects Proteins Regulation RNA, Messenger - metabolism Spleen - immunology Spleen - parasitology Spleen - pathology Th1 Cells - immunology Th1 Cells - metabolism Toll-like receptors Transfection Vector-borne diseases Viral infections |
title | Critical role of IRF-5 in the development of T helper 1 responses to Leishmania donovani infection |
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