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Requirement of thymus-derived theta-positive lymphocytes for rejection of DNA virus (SV 40) tumors in mice.
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1974
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Dna VirusLaboratory ImmunologyAdaptive Immune SystemImmunologyImmune RegulationImmunodominanceImmunologic MechanismImmunotherapeuticsImmunotherapyCancer-associated VirusNylon Wool ColumnTumor ImmunityRadiation OncologyCell TransplantationImmune LymphocytesVirologyImmune SurveillanceSv40 Tumor CellsHumoral ImmunityT Cell ImmunityCell BiologyCancer ImmunosurveillanceThymus-derived Theta-positive LymphocytesSv 40MedicineViral OncologyViral Immunity
The nature of lymphocytes capable of inhibiting the growth of syngeneic papovavirus SV40 tumor cells in BALB/c was investigated by the tumor cell neutralization assay. Treatment of immune lymphocytes with anti-C3H (θ) AKR sera in the presence of complement eliminated the lymphocytes capable of inhibiting tumor cells in vivo. Treatment of immune lymphocytes with normal AKR sera and complement had no effect. Lymphocytes filtered through nylon wool column, a procedure known to remove B lymphocytes, retained their capacity to inhibit tumor cells in vivo. Thymectomized, irradiated, and reconstituted mice failed to develop lymphocytes sensitized to SV40 tumor-specific transplantation antigen (TSTA). These results suggest that cellular immune response to SV40 tumor cells in syngeneic mice is mediated by θ-positive thymus-derived lymphocytes.