Invasive
fungal disease (IFD) constitutes an increasing health concern due to growing numbers of patients at risk for opportunistic fungal infections. Among the fungi capable of inducing opportunistic infections the
yeast Candida albicans is clinically the most important. Immune evasion proteins like the pH-regulated
antigen 1 (Pra1) and the translation
elongation factor 1 (Tef1), which are expressed on the fungal surface and are also secreted, are major drivers of
pathogenicity. Therefore, novel
monoclonal antibodies (mAb) binding these proteins have been developed. In an
in vivo mouse model of high-
dose septic C. albicans infection, therapeutic application of mAb against Pra1 reduced clinical symptoms of the
disease. Prophylactically, mAb against Tef1 protected mice from
clinical disease and prolonged survival. The mABs of the present invention may also be efficacious in patients at risk or with already established IFD.