On the other hand, the moderate agreement of post-acute (63.4%) and recovery (68.7%) stage classification by VIDAS® Dengue assays is in line with the partial concordance with competitor ELISA of the VIDAS® Anti-DENGUE IgM assay (PPA of 74.8% in post-acute samples, NPA of 76.2% in recovery samples) and to some extent of the VIDAS® Anti-DENGUE IgG assay (PPA of 80.5% in post-acute samples). This evidence concerns the gene CD40LG and dengue disease.