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. 2023 Feb 14;56(2):420–432.e7. doi: 10.1016/j.immuni.2023.01.013

Figure 2.

Figure 2

Pfs230-C1 mAbs show a range of functional activity in standard membrane feeding assay

(A) mAbs were tested at 100 μg/mL in parallel in the same membrane feeding experiment. Transmission-reducing activity (TRA) is reduction in oocyst intensity, compared with negative control, and error bars indicate 95% confidence intervals. Antibodies are grouped and colored by domain specificity and epitope bin. No binning data are available for RUPA-103, but it is genetically similar to RUPA-97 (VH and VL amino acid sequence homology >95%) and therefore grouped with other antibodies from bin I.

(B) mAbs that showed >80% TRA in (A) were tested at 100 μg/mL in the presence (+C) or absence (−C) of complement in two independent membrane-feeding experiments, except for RUPA-32 and RUPA-97 that were tested in a single experiment due to limited mAb availability. The complement-dependent rodent α-Pfs230 mAb 2A224 was tested at 10 μg/mL and used as positive control. Bars are estimates of the mean from two independent standard membrane feeding experiments, and error bars represent the 95% confidence intervals.

(C) Titrations of active mAbs were tested in multiple independent membrane feeding assays in the presence of complement to calculate IC80 values, using linear regression analysis. IC80 values with 95% confidence intervals are shown next to graph. Raw SMFA data can be found in Table S2.