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
Hauptverfasser: Ramos, Gerardo, Nghiem, Dat X., Walterscheid, Jeffrey P., Ullrich, Stephen E.
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creator Ramos, Gerardo
Nghiem, Dat X.
Walterscheid, Jeffrey P.
Ullrich, Stephen E.
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. 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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><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Candida albicans - immunology</subject><subject>Chemical and industrial products toxicology. 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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.</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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