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Infection and Immunity, March 1999, p. 1521-1525, Vol. 67, No. 3
Department of Immunology and Molecular
Biology, U.S. Army Medical Research Institute of Infectious
Diseases, Fort Detrick, Maryland
21702-5011,1 and Shippensburg
University, Shippensburg, Pennsylvania 172572
Received 1 September 1998/Returned for modification 17 November
1998/Accepted 22 December 1998
This study describes a quick (<12 h) assay for detecting
temperature decreases in BALB/c and C57BL/6 mice injected
intraperitoneally (i.p.) with staphylococcal enterotoxin A (SEA), SEB,
or SEC3 or toxic shock syndrome toxin 1 and a potentiating dose of
lipopolysaccharide (LPS). Toxin-specific antisera effectively
neutralized the temperature fluctuations in this model. Orally
administered SEA or SEB (50 µg/animal), with or without LPS, did not
have an effect on temperature or lethality. Versus wild-type mice,
transgenic knockout mice lacking the p55 receptor for tumor necrosis
factor (TNF) or gamma interferon were protected against an i.p.
challenge of SEA plus LPS. The p75 receptor for TNF and intercellular
adhesion molecule 1 have a negligible role in this toxic shock model.
0019-9567/99
Correlation of Temperature and Toxicity in Murine
Studies of Staphylococcal Enterotoxins and Toxic Shock Syndrome
Toxin 1
*
Corresponding author. Mailing address: Department of
Immunology and Molecular Biology, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Md. 21702-5011. Phone: (301) 619-4809. Fax: (301) 619-2348. E-mail:
dr.bradleystiles{at}detrick.army.mil.
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