Inhibition of allostimulated HLA-DQ and DP-specific T cells by staphylococcal enterotoxin A

Research output: Contribution to journalJournal articleResearchpeer-review

  • S Masewicz
  • J A Ledbetter
  • P Martin
  • E Mickelson
  • J A Hansen
  • Ødum, Niels
Bacterial superantigens have two immunologically important features. They bind MHC class II molecules and stimulate T cells bearing certain V beta TCR phenotypes. Superantigens such as SEA, SEB, and TSST bind to each of the three HLA class II isotypes (DR, DQ, and DP). Allotypic variation seems to play an important role in superantigen binding to class II molecules, but the functional implications of these differences remain largely unknown. In the present investigation, we studied the effects of SEA, SEB, and TSST on allostimulation of HLA-DR-, DQ-, and DP-allospecific T-cell clones. To avoid direct stimulation of T-cell responses by the superantigens, SEA and/or SEB nonresponsive T-cell clones were selected. We show that SEA strongly inhibited DQ- and DP-specific T-cell responses. In contrast, SEB and TSST had only weak inhibitory effects. DR-specific T-cell responses were unaffected or only weakly inhibited by the superantigens tested. The inhibition appeared not to be due to induction of cytotoxicity or suppression of either T cells or EBV-LCLs by SEA. In conclusion, the bacterial superantigen SEA can block alloantigen-specific stimulation of T clones in vitro. These results suggest that SEA binds to certain MHC class II molecules in a way that prevents MHC-TCR interactions.
Original languageEnglish
JournalHuman Immunology
Volume36
Issue number3
Pages (from-to)142-8
Number of pages6
ISSN0198-8859
Publication statusPublished - 1993

Bibliographical note

Keywords: Antigens, Bacterial; Bacterial Toxins; Enterotoxins; HLA-DP Antigens; HLA-DQ Antigens; Humans; Immune Tolerance; Isoantigens; Lymphocyte Activation; Receptors, Antigen, T-Cell, alpha-beta; Staphylococcus aureus; Superantigens; T-Lymphocyte Subsets

ID: 10636127