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The P. vivax PvCSP peptide and PvCSP tetramer/Fab molecules had similar levels of binding IgG in infected patients and those not infected as determined by ELISA. However, it was encouraging to see that sera from vivax-infected patients had significant Fab inhibitory activity against PvCSP proteins expressed in the yeast *P. pastoris* \[[@B17]\]. In addition, patient sera containing high levels of PvCSP-specific IgG also possessed a capacity to inhibit binding of the PvCSP tetramer/Fab to malaria-naïve RBCs, a result that is consistent with our previous studies on inhibitory antibodies to various malaria proteins. One caveat of this study is that IgG from vivax-infected patients were only assessed for their inhibitory capacity to bind to PfCSP-chimera RBCs *in vitro*, and the utility of IgG from
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