Accessory molecule interactions can be critical in determining the out
come of a T cell's encounter with antigen, Cell adhesion proteins may
augment T cell responses by facilitating TCR engagement of the antigen
-MHC complex, while co-stimulatory molecules may deliver distinct sign
als that modulate T cell responsiveness. CD43 (leukosialin, sialophori
n) has been suggested to influence cell activation by steric hindrance
based upon the large size and glycosylation of the protein, as well a
s the relative abundance of the protein on the cell surface. In this p
aper we examine both in vitro and in vivo T cell-dependent responses i
n CD43-deficient mice. We demonstrate that T cells from CD43-deficient
mice are hyper-responsive following both in vivo and in vitro activat
ion, and that this is observed in response to not only TCR-CD3-mediate
d stimulation, but also following receptor-independent activation. Thi
s data suggests that mechanisms other than non-specific steric hindran
ce are important in the regulation of T cell activation by CD43.