Tumors of diverse origin have recently been shown to express CD95 liga
nd and to induce apoptosis in CD95-expressing targets in vitro; howeve
r, in vivo, enhanced tumor growth and rejection have both been observe
d as a consequence of either immunosuppressive or proinflammatory func
tions of CD95 ligand. The final in vivo outcome of CD95 ligand express
ion will depend upon a complex balance of interactions relevant for ea
ch tumor in its particular microenvironment.