Abstract

Abstract Sheep erythrocytes (E) and mouse mammary tumor cells (MM102) were sensitized with F(ab′)2 antibodies which had been prepared by pepsin digestion after passage through a Sepharose column coupled with anti-Fc to remove intact IgG. Those cells were lyzed at the incubation with rabbit serum (RaS) or guinea pig serum (GPS). Since E-F(ab′)2 did not fix C1 (E-F(ab′)2 was incubated with purified C1, and the fixed C1 to the cells was examined with C1 transfer to EAC4) and did not react with 125I-anti-Fc, the possibility was excluded that intact IgG antibodies had been remaining in the F(ab′)2 fraction. However no hemolysis of E-F(ab′)2 was observed at the incubation with C4-deficient GPS. To examine the effect of natural antibody, E, E-IgG (slightly sensitized) as well as E-F(ab′)2 were treated with EDTA-serum and the cells were incubated with 1/40 GPS after washing with GVB++. By the treatment with EDTA-serum, the hemolysis of E-F(ab′)2 was remarkably enhanced.

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