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Toxins 2012, 4(9), 718-728; doi:10.3390/toxins4090718
Brief Report

Intranasal Rapamycin Rescues Mice from Staphylococcal Enterotoxin B-Induced Shock

*  and
Integrated Toxicology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD 21702, USA
* Author to whom correspondence should be addressed.
Received: 2 July 2012 / Revised: 6 August 2012 / Accepted: 13 August 2012 / Published: 18 September 2012
(This article belongs to the collection Toxicity and Therapeutic Interventions in the Immune System)
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Staphylococcal enterotoxin B (SEB) and related exotoxins produced by Staphylococcus aureus are potent activators of the immune system and cause toxic shock in humans. Currently there is no effective treatment except for the use of intravenous immunoglobulins administered shortly after SEB exposure. Intranasal SEB induces long-lasting lung injury which requires prolonged drug treatment. We investigated the effects of rapamycin, an immunosuppressive drug used to prevent graft rejection, by intranasal administration in a lethal mouse model of SEB-induced shock. The results show that intranasal rapamycin alone delivered as late as 17 h after SEB protected 100% of mice from lethal shock. Additionally, rapamycin diminished the weight loss and temperature fluctuations elicited by SEB. Intranasal rapamycin attenuated lung MCP-1, IL-2, IL-6, and IFNγ by 70%, 30%, 64%, and 68% respectively. Furthermore, short courses (three doses) of rapamycin were sufficient to block SEB-induced shock. Intranasal rapamycin represents a novel use of an immunosuppressant targeting directly to site of toxin exposure, reducing dosages needed and allowing a wider therapeutic window.
Keywords: intranasal rapamycin; staphylococcal enterotoxin B; shock intranasal rapamycin; staphylococcal enterotoxin B; shock
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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Krakauer, T.; Buckley, M. Intranasal Rapamycin Rescues Mice from Staphylococcal Enterotoxin B-Induced Shock. Toxins 2012, 4, 718-728.

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