Staphylococcal superantigens interact with multiple host receptors to cause serious diseases

Christopher S. Stach, Alfa Herrera, Patrick M. Schlievert

Research output: Contribution to journalReview articlepeer-review

46 Scopus citations


Staphylococcus aureus strains that cause human diseases produce a large family of pyrogenic toxin superantigens (SAgs). These include toxic shock syndrome toxin-1 (TSST-1), the staphylococcal enterotoxins (SEs), and the SE-like proteins; to date, 23 staphylococcal SAgs have been described. Among the SAgs, three have been highly associated with human diseases (TSST-1, SEB, and SEC), likely because they are produced in high concentrations compared to other SAgs. Another major family of exotoxins produced by S. aureus is the cytolysins, particularly α-, β-, γ-, and δ-toxins, phenol soluble modulins, and leukocidins. This review discusses the association of SAgs with human diseases and particularly the "outside-in" signaling mechanism that leads to SAg-associated diseases. We discuss SAg interactions with three host immune cell receptors, including variable regions of the β-chain of the T cell receptor, MHC II α- and/or β-chains, and an epithelial/endothelial cell receptor that may include CD40. To a lesser extent, we discuss the role of cytolysins in facilitating disease production by SAgs.

Original languageEnglish (US)
Pages (from-to)177-181
Number of pages5
JournalImmunologic Research
Issue number1-3
StatePublished - Aug 2014


  • Menstrual toxic shock
  • Superantigen
  • TSST-1
  • Toxic shock syndrome toxin


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