Fig. 9.
Effect of mγ3-anti-CD3ɛ and mitogenic anti-CD3ɛ administration on APC functions. Spleen cells from control antibody-treated mice, mγ3-anti-CD3ɛ–treated mice, or anti-CD3ɛ–treated mice (50 μg IV) were irradiated and used as accessory cells to stimulate G10-nonadherent responding cells from CBA mice (3 × 105/well). Results are expressed as cpm of [3H] TdR incorporation by responder cells.