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. 2014 Dec 4;159(6):1277–1289. doi: 10.1016/j.cell.2014.10.053

Figure 5.

Figure 5

Protective Effect of Anti-α-Gal Abs

(A) Relative absorbance of anti-α-gal Abs (Mean ± SD) in serial serum dilutions from nonimmunized (NI) or rRBCM-immunized (I) α1,3Gt−/− mice (two experiments; n = 10).

(B) Incidence of blood stage infection (%) in specific immune component-deleted α1,3Gt−/− mice immunized (I) or not (NI) as in (A) and exposed to PbAEEF1a-GFP-infected mosquitoes (3–7 experiments; n = 13–41).

(C) Incidence of blood stage of infection (%) in α1,3Gt−/− mice after passive transfer of anti-α-gal Abs versus controls (no passive transfer; ctr.) exposed to PbAEEF1a-GFP-infected mosquitoes (4–7 experiments; n = 19–32).

(D) C3 deposition in PbAHsp70-GFP sporozoites not exposed (ctr.) or exposed to anti-α-gal Abs plus mouse complement (C). Representative of three independent experiments.

(E) Incidence of blood stage of infection (%) in α1,3Gt−/−C3−/− mice after passive transfer of anti-α-gal IgM (μ), IgG2b (γ2b), or IgG3 (γ3) Abs versus controls (ctr.; no passive transfer) not receiving Abs, exposed to PbAEEF1a-GFP-infected mosquitoes (four experiments; n = 21–37).

(F) Same as (E) in PMN-depleted α1,3Gt−/− mice (four experiments; n = 15–25).

See also Figures S5 and S6.