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PMID: 11544350 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Toxic shock syndrome and bacterial superantigens: an update.

Annual review of microbiology ·Vol. 55 ·2001-00-00 ·Pages 77-104

McCormick JK, Yarwood JM, Schlievert PM

Abstract

Toxic shock syndrome (TSS) is an acute onset illness characterized by fever, rash formation, and hypotension that can lead to multiple organ failure and lethal shock, as well as desquamation in patients that recover. The disease is caused by bacterial superantigens (SAGs) secreted from Staphylococcus aureus and group A streptococci. SAGs bypass normal antigen presentation by binding to class II major histocompatibility complex molecules on antigen-presenting cells and to specific variable regions on the beta-chain of the T-cell antigen receptor. Through this interaction, SAGs activate T cells at orders of magnitude above antigen-specific activation, resulting in massive cytokine release that is believed to be responsible for the most severe features of TSS. This review focuses on clinical and epidemiological aspects of TSS, as well as important developments in the genetics, biochemistry, immunology, and structural biology of SAGs. From the evolutionary relationships between these important toxins, we propose that there are five distinct groups of SAGs.

MeSH Terms
Amino Acid Sequence Humans Molecular Sequence Data Sequence Alignment Shock, Septic/diagnosis,epidemiology,microbiology Staphylococcus aureus/immunology Streptococcus pyogenes/immunology Superantigens/chemistry,genetics,immunology
Chemicals
Superantigens
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
McCormick J K
Department of Microbiology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA. jmccormi@lenti.med.umn.edu
Yarwood J M
Schlievert P M
Article Info
Journal
Annual review of microbiology
Abbr.
Annu Rev Microbiol
ISSN
0066-4227
Published
2001-00-00
Pages
77-104
Language
English
Region
United States
NLM ID
0372370
Subset
IM
Grants
NIAID NIH HHS · AI22159 · United States
NHLBI NIH HHS · HL36611 · United States
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