Cellular requirements for the monoclonal antibody-mediated eradication of an established solid tumor

Following subcutaneous implantation, the murine lymphoma E.G7 [a variant of EL-4, transfected with the chicken ovalbumin (OVA) gene] up-regulates the CD4 molecule. We previously showed that the administration of an anti-CD4 m onoclonal antibody (mAb) to EG.7-bearing mice leads to a rapid and complete regression of large established tumors. This tumor regression was shown to require both CD8(+) cells and functional Fc gamma receptors (Fc gamma R), as it failed to occur in mice depleted of CD8 cells, or mice genetically de ficient in Fc gamma RI/III (gamma(-/-) mice). Using adoptive transfer, we n ow show that the Fc gamma R+ cells required for this regression are the CD1 1b(+) (phagocytic) cells. Furthermore, experiments using peptide tolerizati on demonstrated that the critical CD8 CTL population in this model is tumor specific. Analysis of tumors at various stages of regression revealed a ma ssive CD11b(+) Fc gamma R+ and a marginal CD8 infiltration. In the presence of the CTL determinant OVA-8 on tumor cells and of the antitumor mAb, this CD8 infiltration became remarkable, and correlated with tumor regression. These results identify the specific cellular effecters essential for the mA b-mediated tumor regression, and suggest that Fc gamma R-activated macropha ges induced an expansion of tumor-eliminating CTL in situ.