Figure 5.
Figure 5. Purified IgM confers ABO serum sensitivity to virions. (A) Inhibition of serum inactivation by excess soluble blood group antigens. SF-2 virus grown in PBMCs from an A donor was assayed for serum sensitivity in O and A sera as before, in the presence or absence of 10 μg soluble A trisaccharide. (B) IgM from ABO sera differentially sensitizes virus to guinea pig complement. SF-2 derived from an A donor was incubated with varying concentrations of IgM purified from ABO-defined donor sera in the presence of active guinea pig complement (C′) or a heat-inactivated control. Diamonds (♦), squares (▪), and triangles (▴) represent viral infections in the presence of IgM from O, A, or B sera, respectively. HIV-1 NL4-3 raised in 293T cells transfected with αGal(1-3)galactosyltransferase was treated similarly as a control for antibody-dependent serum sensitivity. Both viruses were plated on NP2CD4X4 cells and processed as before.

Purified IgM confers ABO serum sensitivity to virions. (A) Inhibition of serum inactivation by excess soluble blood group antigens. SF-2 virus grown in PBMCs from an A donor was assayed for serum sensitivity in O and A sera as before, in the presence or absence of 10 μg soluble A trisaccharide. (B) IgM from ABO sera differentially sensitizes virus to guinea pig complement. SF-2 derived from an A donor was incubated with varying concentrations of IgM purified from ABO-defined donor sera in the presence of active guinea pig complement (C′) or a heat-inactivated control. Diamonds (♦), squares (▪), and triangles (▴) represent viral infections in the presence of IgM from O, A, or B sera, respectively. HIV-1 NL4-3 raised in 293T cells transfected with αGal(1-3)galactosyltransferase was treated similarly as a control for antibody-dependent serum sensitivity. Both viruses were plated on NP2CD4X4 cells and processed as before.

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