We have previously shown that one of the co-factors required for gener
ation of T-cell responses, B7.1, is variably expressed on melanoma cel
ls. In the present studies we have examined the expression of another
important co-factor in T-cell responses, viz., CD40, and investigated
regulation of its expression and possible function(s). PCR analysis re
vealed mRNA for CD40 in alt 18 cell lines established from metastatic
melanoma and the majority of those from 6 primary melanoma. CD40 prote
in was detectable in approximately 50% of the cell lines by now cytome
try and in sections from only 2 of 20 melanoma. Expression of CD40 pro
tein was increased in 2 of 3 cell lines with constitutive CD40 express
ion by interferon-gamma but not by granulocyte/macrophage colony-stimu
lating factor, interleukin-2 or tumor necrosis factor-alpha. Interacti
on of monoclonal antibody with CD40 on melanoma cells resulted in an i
ncrease in their cell division but did not increase expression of the
co-stimulatory factor B7. Our results suggest that CD40 expression on
melanoma may have important effects on their biology. The influence of
CD40 expression on T-cell responses to melanoma remains to be investi
gated. (C) 1996 Wiley-Liss, Inc.