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Lytic activity of serum and different sera-derived factors against Trypanosoma cruzi was investigated and purified by the procedure of affinity chromatography on Sephadex G-100. The most active fractions derived from serum, and also from 4 out of 5 human sera tested, lysed Y-chromosome-bearing trypomastigotes, belonging to a clone selected from a homogeneous variant of virulent Y strain (Y3). This activity was completely abrogated by rabbit anti-mouse IgG antibody, factor F(ab)2 fragments prepared from both IgG2b and IgG2a immunized mice, and anti-IgG2b mAb. The IgG fraction depleted by protein A chromatography from human immune sera lysed Y3 trypomastigotes, but not those from a clone selected from non-virulent RA strain, and lysed a third clone selected from cross-hybridized Y and RA strains (Y12). The IgG activity was also detected in supernatants of spleen cell cultures stimulated with T. cruzi lysate. It was not neutralized by anti-IgG2a mAb, and was suppressed by anti-IgG3, anti-IgG1, or anti-Fc gamma RI mAb, but not by anti-Fc gamma RII mAb, suggesting an IgG1-dependent activity. When tested for activity against epimastigotes, this IgG factor was not detectable in mouse sera and was completely abolished when cell culture supernatants, but not serum, were used. IgG-mediated lysis was proportional to parasite viability, since it depended on the presence of intracellular parasites and completely neutralized by the addition of cycloheximide to cultures. It was also similar in magnitude to sera-mediated lysis. The IgG-mediated lysis was not blocked by antisera against Thy-1, Ia or class-II MHC proteins, and did not kill the parasite in vitro, suggesting that it was not dependent on
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