Renal tubular epithelial cells (TEC) can express MHC class II molecule
s in vitro and in vivo. Their ability to also secrete cytokines and ex
press adhesion molecules suggests a possible immune accessory role for
TEC. We have previously documented that TEC process and present antig
en to T cell hybridomas. However, engagement of the T cell receptor al
one is sufficient to induce IL-2 secretion by T cell hybridomas. We no
w report that presentation of antigen by TEC to a CD4+ T cell clone re
sults in functional inactivation of the T cells. Despite antigen-speci
fic anergy, these T cells are viable and proliferate in response to IL
-2. Furthermore, allogeneic antigen presenting cells were unable to re
store the T cell proliferative response, suggesting that the mechanism
(s) was not entirely costimulator-dependent.