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Deficiency of IL-12p40 subunit determines severe paracoccidioidomycosis in mice
Paracoccidioidomycosis, the major systemic mycosis in Latin America, is caused by the thermally dimorphic fungus Paracoccidioides brasiliensis. To investigate the role of interleukin (IL)-12 in this disease, IL-12p40-/- deficient mice (IL-12p40-/-) and wild type mice (WT) were infected intravenously...
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Published in: | Medical mycology (Oxford) 2008-11, Vol.46 (7), p.637-646 |
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description | Paracoccidioidomycosis, the major systemic mycosis in Latin America, is caused by the thermally dimorphic fungus Paracoccidioides brasiliensis. To investigate the role of interleukin (IL)-12 in this disease, IL-12p40-/- deficient mice (IL-12p40-/-) and wild type mice (WT) were infected intravenously with viable yeast cells of P. brasiliensis 18 isolate. We found that, unlike WT mice, IL-12p40-/- mice did not control fungal proliferation and dissemination and succumbed to infection by day 21 after inoculation. Additionally, IL-12p40-/- mice presented a higher number of granulomas/mm2 in lung tissue than WT mice, and showed unorganized granulomas containing high numbers of yeast cells. Moreover, IL-12p40-/- mice did not release detectable levels of IFN- , but they produced high levels of IL-10, as well as IgG1 antibody. Additionally, splenocytes from both infected IL-12p40-/- and WT mice exhibited a suppressed Con-A-induced T cell proliferative response. Our findings suggest that the IL-12p40 subunit mediates resistance in paracoccidioidomycosis by inducting IFN- production and a Th1 immune response |
doi_str_mv | 10.1080/13693780801982762 |
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To investigate the role of interleukin (IL)-12 in this disease, IL-12p40-/- deficient mice (IL-12p40-/-) and wild type mice (WT) were infected intravenously with viable yeast cells of P. brasiliensis 18 isolate. We found that, unlike WT mice, IL-12p40-/- mice did not control fungal proliferation and dissemination and succumbed to infection by day 21 after inoculation. Additionally, IL-12p40-/- mice presented a higher number of granulomas/mm2 in lung tissue than WT mice, and showed unorganized granulomas containing high numbers of yeast cells. Moreover, IL-12p40-/- mice did not release detectable levels of IFN- , but they produced high levels of IL-10, as well as IgG1 antibody. Additionally, splenocytes from both infected IL-12p40-/- and WT mice exhibited a suppressed Con-A-induced T cell proliferative response. Our findings suggest that the IL-12p40 subunit mediates resistance in paracoccidioidomycosis by inducting IFN- production and a Th1 immune response</description><identifier>ISSN: 1369-3786</identifier><identifier>EISSN: 1460-2709</identifier><identifier>DOI: 10.1080/13693780801982762</identifier><identifier>PMID: 18608917</identifier><language>eng</language><publisher>UK: Informa UK Ltd</publisher><subject>Animals ; Antibodies, Fungal - blood ; Cell Proliferation ; Colony Count, Microbial ; Female ; Granuloma, Foreign-Body - microbiology ; Granuloma, Foreign-Body - pathology ; Immunoglobulin G - metabolism ; Interferon-gamma - metabolism ; Interleukin-10 - metabolism ; Interleukin-12 Subunit p40 - deficiency ; Interleukin-12 Subunit p40 - genetics ; Lung - immunology ; Lung - microbiology ; Lung - pathology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Paracoccidioides - immunology ; Paracoccidioidomycosis - genetics ; Paracoccidioidomycosis - immunology ; Paracoccidioidomycosis - mortality ; Paracoccidioidomycosis - pathology ; Spleen - immunology ; Spleen - microbiology ; Survival Analysis ; T-Lymphocytes - cytology ; T-Lymphocytes - immunology</subject><ispartof>Medical mycology (Oxford), 2008-11, Vol.46 (7), p.637-646</ispartof><rights>2008 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2008</rights><rights>2008 International Society for Human and Animal Mycology 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-bf1fa8cd60ed02c6080acedf7b3557c448531f5fa46841921c32e63c4913494a3</citedby><cites>FETCH-LOGICAL-c462t-bf1fa8cd60ed02c6080acedf7b3557c448531f5fa46841921c32e63c4913494a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18608917$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Livonesi, Márcia Cristina</creatorcontrib><creatorcontrib>Souto, Janeusa Trindade</creatorcontrib><creatorcontrib>Campanelli, Ana Paula</creatorcontrib><creatorcontrib>Leite Maffei, Cláudia M.</creatorcontrib><creatorcontrib>Martinez, Roberto</creatorcontrib><creatorcontrib>Rossi, Marcos A.</creatorcontrib><creatorcontrib>Silva, João Santana Da</creatorcontrib><title>Deficiency of IL-12p40 subunit determines severe paracoccidioidomycosis in mice</title><title>Medical mycology (Oxford)</title><addtitle>Med Mycol</addtitle><description>Paracoccidioidomycosis, the major systemic mycosis in Latin America, is caused by the thermally dimorphic fungus Paracoccidioides brasiliensis. To investigate the role of interleukin (IL)-12 in this disease, IL-12p40-/- deficient mice (IL-12p40-/-) and wild type mice (WT) were infected intravenously with viable yeast cells of P. brasiliensis 18 isolate. We found that, unlike WT mice, IL-12p40-/- mice did not control fungal proliferation and dissemination and succumbed to infection by day 21 after inoculation. Additionally, IL-12p40-/- mice presented a higher number of granulomas/mm2 in lung tissue than WT mice, and showed unorganized granulomas containing high numbers of yeast cells. Moreover, IL-12p40-/- mice did not release detectable levels of IFN- , but they produced high levels of IL-10, as well as IgG1 antibody. Additionally, splenocytes from both infected IL-12p40-/- and WT mice exhibited a suppressed Con-A-induced T cell proliferative response. Our findings suggest that the IL-12p40 subunit mediates resistance in paracoccidioidomycosis by inducting IFN- production and a Th1 immune response</description><subject>Animals</subject><subject>Antibodies, Fungal - blood</subject><subject>Cell Proliferation</subject><subject>Colony Count, Microbial</subject><subject>Female</subject><subject>Granuloma, Foreign-Body - microbiology</subject><subject>Granuloma, Foreign-Body - pathology</subject><subject>Immunoglobulin G - metabolism</subject><subject>Interferon-gamma - metabolism</subject><subject>Interleukin-10 - metabolism</subject><subject>Interleukin-12 Subunit p40 - deficiency</subject><subject>Interleukin-12 Subunit p40 - genetics</subject><subject>Lung - immunology</subject><subject>Lung - microbiology</subject><subject>Lung - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Paracoccidioides - immunology</subject><subject>Paracoccidioidomycosis - genetics</subject><subject>Paracoccidioidomycosis - immunology</subject><subject>Paracoccidioidomycosis - mortality</subject><subject>Paracoccidioidomycosis - pathology</subject><subject>Spleen - immunology</subject><subject>Spleen - microbiology</subject><subject>Survival Analysis</subject><subject>T-Lymphocytes - cytology</subject><subject>T-Lymphocytes - immunology</subject><issn>1369-3786</issn><issn>1460-2709</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkM1LJDEQxcPisn7s_gFepE-ebE0l6XQHTzJ-woCX3XOTqa5gZLrTJt3C_PdmmQEPgnqqB_V7j6rH2DHwc-ANvwCpjaybLME0otbiBzsApXkpam72ss77MgN6nx2m9Mw51EbIX2wfGs0bA_UBe7wm59HTgJsiuOJhWYIYFS_SvJoHPxUdTRR7P1AqEr1SpGK00WJA9J0Pvgv9BkPyqfBD0Xuk3-yns-tEf3bziP27vfm7uC-Xj3cPi6tliUqLqVw5cLbBTnPquMB8DbdInatXsqpqVKqpJLjKWaUbBUYASkFaojIglVFWHrHTbe4Yw8tMaWp7n5DWaztQmFOrTX6xquBLUHBe1UKJDMIWxBhSiuTaMfrexk0LvP1fd_uh7uw52YXPq566d8eu3wycbYEwj9_Ku9zifnAh9vaJ7Hp6QhupfQ5zHHKjn7jfAGO2mHg</recordid><startdate>200811</startdate><enddate>200811</enddate><creator>Livonesi, Márcia Cristina</creator><creator>Souto, Janeusa Trindade</creator><creator>Campanelli, Ana Paula</creator><creator>Leite Maffei, Cláudia M.</creator><creator>Martinez, Roberto</creator><creator>Rossi, Marcos A.</creator><creator>Silva, João Santana Da</creator><general>Informa UK Ltd</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>7QL</scope><scope>C1K</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>200811</creationdate><title>Deficiency of IL-12p40 subunit determines severe paracoccidioidomycosis in mice</title><author>Livonesi, Márcia Cristina ; 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To investigate the role of interleukin (IL)-12 in this disease, IL-12p40-/- deficient mice (IL-12p40-/-) and wild type mice (WT) were infected intravenously with viable yeast cells of P. brasiliensis 18 isolate. We found that, unlike WT mice, IL-12p40-/- mice did not control fungal proliferation and dissemination and succumbed to infection by day 21 after inoculation. Additionally, IL-12p40-/- mice presented a higher number of granulomas/mm2 in lung tissue than WT mice, and showed unorganized granulomas containing high numbers of yeast cells. Moreover, IL-12p40-/- mice did not release detectable levels of IFN- , but they produced high levels of IL-10, as well as IgG1 antibody. Additionally, splenocytes from both infected IL-12p40-/- and WT mice exhibited a suppressed Con-A-induced T cell proliferative response. 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subjects | Animals Antibodies, Fungal - blood Cell Proliferation Colony Count, Microbial Female Granuloma, Foreign-Body - microbiology Granuloma, Foreign-Body - pathology Immunoglobulin G - metabolism Interferon-gamma - metabolism Interleukin-10 - metabolism Interleukin-12 Subunit p40 - deficiency Interleukin-12 Subunit p40 - genetics Lung - immunology Lung - microbiology Lung - pathology Male Mice Mice, Inbred C57BL Mice, Knockout Paracoccidioides - immunology Paracoccidioidomycosis - genetics Paracoccidioidomycosis - immunology Paracoccidioidomycosis - mortality Paracoccidioidomycosis - pathology Spleen - immunology Spleen - microbiology Survival Analysis T-Lymphocytes - cytology T-Lymphocytes - immunology |
title | Deficiency of IL-12p40 subunit determines severe paracoccidioidomycosis in mice |
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