Dermal Application of Jet Fuel Suppresses Secondary Immune Reactions
Applying military jet fuel (JP-8) to the skin of mice activates systemic immune suppression. In all of our previous experiments, JP-8 was applied to immunologically naı̈ve mice. The effect of jet fuels on established immune reactions, such as immunological memory, is unknown. The focus of the experi...
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Veröffentlicht in: | Toxicology and applied pharmacology 2002-04, Vol.180 (2), p.136-144 |
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description | Applying military jet fuel (JP-8) to the skin of mice activates systemic immune suppression. In all of our previous experiments, JP-8 was applied to immunologically naı̈ve mice. The effect of jet fuels on established immune reactions, such as immunological memory, is unknown. The focus of the experiments presented here was to test the hypothesis that jet fuel exposure [both JP-8 and commercial jet fuel (Jet-A)] suppresses established immune reactions. Mice were immunized with the opportunistic fungal pathogen Candida albicans and, at different times after immunization (10 to 30 days), various doses of undiluted JP-8 or Jet-A were applied to their skin. Both the elicitation of delayed-type hypersensitivity (DTH) (mice challenged 10 days after immunization) and immunological memory (mice challenged 30 days after immunization) were significantly suppressed in a dose-dependent manner. Dermal exposure to either multiple small doses (50 μl over 4 days) or a single large dose (≈200–300 μl) of JP-8 and/or Jet-A suppressed DTH to C. albicans. The mechanism by which dermal application of JP-8 and Jet-A suppresses immunological memory involves the release of immune biologic response modifiers. Blocking the production of prostaglandin E2 by a selective cyclooxygenase-2 inhibitor (SC 236) significantly reversed jet fuel-induced suppression of immunologic memory. These findings indicate, for the first time, that dermal exposure to commercial jet fuel (Jet-A) suppresses the immune response. In addition, the data reported here expand on previous findings by suggesting that jet fuel exposure may depress the protective effect of prior vaccination. |
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In all of our previous experiments, JP-8 was applied to immunologically naı̈ve mice. The effect of jet fuels on established immune reactions, such as immunological memory, is unknown. The focus of the experiments presented here was to test the hypothesis that jet fuel exposure [both JP-8 and commercial jet fuel (Jet-A)] suppresses established immune reactions. Mice were immunized with the opportunistic fungal pathogen Candida albicans and, at different times after immunization (10 to 30 days), various doses of undiluted JP-8 or Jet-A were applied to their skin. Both the elicitation of delayed-type hypersensitivity (DTH) (mice challenged 10 days after immunization) and immunological memory (mice challenged 30 days after immunization) were significantly suppressed in a dose-dependent manner. Dermal exposure to either multiple small doses (50 μl over 4 days) or a single large dose (≈200–300 μl) of JP-8 and/or Jet-A suppressed DTH to C. albicans. The mechanism by which dermal application of JP-8 and Jet-A suppresses immunological memory involves the release of immune biologic response modifiers. Blocking the production of prostaglandin E2 by a selective cyclooxygenase-2 inhibitor (SC 236) significantly reversed jet fuel-induced suppression of immunologic memory. These findings indicate, for the first time, that dermal exposure to commercial jet fuel (Jet-A) suppresses the immune response. In addition, the data reported here expand on previous findings by suggesting that jet fuel exposure may depress the protective effect of prior vaccination.</description><identifier>ISSN: 0041-008X</identifier><identifier>EISSN: 1096-0333</identifier><identifier>DOI: 10.1006/taap.2002.9380</identifier><identifier>PMID: 11969381</identifier><identifier>CODEN: TXAPA9</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Candida albicans - immunology ; Chemical and industrial products toxicology. Toxic occupational diseases ; Cyclooxygenase Inhibitors - pharmacology ; delayed-type hypersensitivity ; Female ; Hydrocarbons - immunology ; Hydrocarbons - toxicity ; Hypersensitivity, Delayed - chemically induced ; Hypersensitivity, Delayed - immunology ; immune suppression ; Immunization ; Immunologic Memory - drug effects ; Immunologic Memory - immunology ; immunotoxicity ; jet fuel ; Jet-A ; JP-8 ; Medical sciences ; Mice ; Mice, Inbred C3H ; prostaglandin E2 ; Pyrazoles - pharmacology ; Skin Absorption - immunology ; Specific Pathogen-Free Organisms ; Sulfonamides - pharmacology ; Toxicology ; Various organic compounds</subject><ispartof>Toxicology and applied pharmacology, 2002-04, Vol.180 (2), p.136-144</ispartof><rights>2002 Elsevier Science (USA)</rights><rights>2002 INIST-CNRS</rights><rights>(c)2002 Elsevier Science (USA).</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-88b7f58eb96ffa6181eba0f59f02a669046dbb29fddf4583af00ba9c64012ec03</citedby><cites>FETCH-LOGICAL-c401t-88b7f58eb96ffa6181eba0f59f02a669046dbb29fddf4583af00ba9c64012ec03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/taap.2002.9380$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13682984$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11969381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramos, Gerardo</creatorcontrib><creatorcontrib>Nghiem, Dat X.</creatorcontrib><creatorcontrib>Walterscheid, Jeffrey P.</creatorcontrib><creatorcontrib>Ullrich, Stephen E.</creatorcontrib><title>Dermal Application of Jet Fuel Suppresses Secondary Immune Reactions</title><title>Toxicology and applied pharmacology</title><addtitle>Toxicol Appl Pharmacol</addtitle><description>Applying military jet fuel (JP-8) to the skin of mice activates systemic immune suppression. In all of our previous experiments, JP-8 was applied to immunologically naı̈ve mice. The effect of jet fuels on established immune reactions, such as immunological memory, is unknown. The focus of the experiments presented here was to test the hypothesis that jet fuel exposure [both JP-8 and commercial jet fuel (Jet-A)] suppresses established immune reactions. Mice were immunized with the opportunistic fungal pathogen Candida albicans and, at different times after immunization (10 to 30 days), various doses of undiluted JP-8 or Jet-A were applied to their skin. Both the elicitation of delayed-type hypersensitivity (DTH) (mice challenged 10 days after immunization) and immunological memory (mice challenged 30 days after immunization) were significantly suppressed in a dose-dependent manner. Dermal exposure to either multiple small doses (50 μl over 4 days) or a single large dose (≈200–300 μl) of JP-8 and/or Jet-A suppressed DTH to C. albicans. The mechanism by which dermal application of JP-8 and Jet-A suppresses immunological memory involves the release of immune biologic response modifiers. Blocking the production of prostaglandin E2 by a selective cyclooxygenase-2 inhibitor (SC 236) significantly reversed jet fuel-induced suppression of immunologic memory. These findings indicate, for the first time, that dermal exposure to commercial jet fuel (Jet-A) suppresses the immune response. In addition, the data reported here expand on previous findings by suggesting that jet fuel exposure may depress the protective effect of prior vaccination.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Candida albicans - immunology</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Cyclooxygenase Inhibitors - pharmacology</subject><subject>delayed-type hypersensitivity</subject><subject>Female</subject><subject>Hydrocarbons - immunology</subject><subject>Hydrocarbons - toxicity</subject><subject>Hypersensitivity, Delayed - chemically induced</subject><subject>Hypersensitivity, Delayed - immunology</subject><subject>immune suppression</subject><subject>Immunization</subject><subject>Immunologic Memory - drug effects</subject><subject>Immunologic Memory - immunology</subject><subject>immunotoxicity</subject><subject>jet fuel</subject><subject>Jet-A</subject><subject>JP-8</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>prostaglandin E2</subject><subject>Pyrazoles - pharmacology</subject><subject>Skin Absorption - immunology</subject><subject>Specific Pathogen-Free Organisms</subject><subject>Sulfonamides - pharmacology</subject><subject>Toxicology</subject><subject>Various organic compounds</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9LwzAUx4Mobk6vHqUXvbW-NF1MjmNzOhkITsFbSNMXiPSXSSv439uywU6e3uXz-fL4EHJNIaEA_L7Tuk1SgDSRTMAJmVKQPAbG2CmZAmQ0BhCfE3IRwhcAyCyj52RCqeQDT6dktUJf6TJatG3pjO5cU0eNjV6wi9Y9ltGub1uPIWCIdmiautD-N9pUVV9j9IbajEK4JGdWlwGvDndGPtaP78vnePv6tFkutrHJgHaxEPmDnQvMJbdWcyoo5hrsXFpINecSMl7keSptUdhsLpi2ALmWhg92igbYjNztd1vffPcYOlW5YLAsdY1NHxQVjLL5YM5IsgeNb0LwaFXrXTW8riiosZsau6mxmxq7DcLNYbnPKyyO-CHUANweAB2MLq3XtXHhyDEuUimygRN7DocOPw69CsZhbbBwHk2nisb998MfZ4WJMQ</recordid><startdate>20020415</startdate><enddate>20020415</enddate><creator>Ramos, Gerardo</creator><creator>Nghiem, Dat X.</creator><creator>Walterscheid, Jeffrey P.</creator><creator>Ullrich, Stephen E.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20020415</creationdate><title>Dermal Application of Jet Fuel Suppresses Secondary Immune Reactions</title><author>Ramos, Gerardo ; Nghiem, Dat X. ; Walterscheid, Jeffrey P. ; Ullrich, Stephen E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-88b7f58eb96ffa6181eba0f59f02a669046dbb29fddf4583af00ba9c64012ec03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Candida albicans - immunology</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Cyclooxygenase Inhibitors - pharmacology</topic><topic>delayed-type hypersensitivity</topic><topic>Female</topic><topic>Hydrocarbons - immunology</topic><topic>Hydrocarbons - toxicity</topic><topic>Hypersensitivity, Delayed - chemically induced</topic><topic>Hypersensitivity, Delayed - immunology</topic><topic>immune suppression</topic><topic>Immunization</topic><topic>Immunologic Memory - drug effects</topic><topic>Immunologic Memory - immunology</topic><topic>immunotoxicity</topic><topic>jet fuel</topic><topic>Jet-A</topic><topic>JP-8</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>prostaglandin E2</topic><topic>Pyrazoles - pharmacology</topic><topic>Skin Absorption - immunology</topic><topic>Specific Pathogen-Free Organisms</topic><topic>Sulfonamides - pharmacology</topic><topic>Toxicology</topic><topic>Various organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramos, Gerardo</creatorcontrib><creatorcontrib>Nghiem, Dat X.</creatorcontrib><creatorcontrib>Walterscheid, Jeffrey P.</creatorcontrib><creatorcontrib>Ullrich, Stephen E.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology and applied pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramos, Gerardo</au><au>Nghiem, Dat X.</au><au>Walterscheid, Jeffrey P.</au><au>Ullrich, Stephen E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dermal Application of Jet Fuel Suppresses Secondary Immune Reactions</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>2002-04-15</date><risdate>2002</risdate><volume>180</volume><issue>2</issue><spage>136</spage><epage>144</epage><pages>136-144</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><coden>TXAPA9</coden><abstract>Applying military jet fuel (JP-8) to the skin of mice activates systemic immune suppression. In all of our previous experiments, JP-8 was applied to immunologically naı̈ve mice. The effect of jet fuels on established immune reactions, such as immunological memory, is unknown. The focus of the experiments presented here was to test the hypothesis that jet fuel exposure [both JP-8 and commercial jet fuel (Jet-A)] suppresses established immune reactions. Mice were immunized with the opportunistic fungal pathogen Candida albicans and, at different times after immunization (10 to 30 days), various doses of undiluted JP-8 or Jet-A were applied to their skin. Both the elicitation of delayed-type hypersensitivity (DTH) (mice challenged 10 days after immunization) and immunological memory (mice challenged 30 days after immunization) were significantly suppressed in a dose-dependent manner. Dermal exposure to either multiple small doses (50 μl over 4 days) or a single large dose (≈200–300 μl) of JP-8 and/or Jet-A suppressed DTH to C. albicans. The mechanism by which dermal application of JP-8 and Jet-A suppresses immunological memory involves the release of immune biologic response modifiers. Blocking the production of prostaglandin E2 by a selective cyclooxygenase-2 inhibitor (SC 236) significantly reversed jet fuel-induced suppression of immunologic memory. These findings indicate, for the first time, that dermal exposure to commercial jet fuel (Jet-A) suppresses the immune response. In addition, the data reported here expand on previous findings by suggesting that jet fuel exposure may depress the protective effect of prior vaccination.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>11969381</pmid><doi>10.1006/taap.2002.9380</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Candida albicans - immunology Chemical and industrial products toxicology. Toxic occupational diseases Cyclooxygenase Inhibitors - pharmacology delayed-type hypersensitivity Female Hydrocarbons - immunology Hydrocarbons - toxicity Hypersensitivity, Delayed - chemically induced Hypersensitivity, Delayed - immunology immune suppression Immunization Immunologic Memory - drug effects Immunologic Memory - immunology immunotoxicity jet fuel Jet-A JP-8 Medical sciences Mice Mice, Inbred C3H prostaglandin E2 Pyrazoles - pharmacology Skin Absorption - immunology Specific Pathogen-Free Organisms Sulfonamides - pharmacology Toxicology Various organic compounds |
title | Dermal Application of Jet Fuel Suppresses Secondary Immune Reactions |
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