Ac. Haffner et al., MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I MOLECULE SELVES AS A LIGAND FOR PRESENTATION OF THE SUPERANTIGEN STAPHYLOCOCCAL-ENTEROTOXIN-B TO T-CELLS, Proceedings of the National Academy of Sciences of the United Statesof America, 93(7), 1996, pp. 3037-3042
Superantigens, such as staphylococcal enterotoxin B (SEE), elicit a st
rong proliferative response in T cells when presented in the context o
f major histocompatibility complex (MHC) class II molecules. We observ
ed a similar T-cell response, when MHC class II-negative epidermal cel
l lines were employed as antigen-presenting cells, Immunoprecipitation
studies indicated that the ligand to which SEE bound had a molecular
mass of 46 kDa, Radiolabeled SEE could be immunoprecipitated from isol
ated membrane proteins on the SCC13 epidermal cell line with a monoclo
nal antibody directed against the MHC class I molecule, and transfecti
on of the K-562 cell line with MHC class I molecules showed a 75% incr
eased SEE-binding capacity compared with the nontransfected MHC class
I- and class II-negative counterpart, In functional studies, antibodie
s to the MHC class I molecule inhibited T-cell proliferation by at lea
st 50%, From these studies, we conclude that MHC class I molecules on
malignant squamous cell carcinomas serve as ligands for SEE, which, gi
ven the appropriate costimulatory signals, is sufficient to allow for
superantigen-induced T-cell proliferation.