In addition to HLA polymorphisms, these include a TRAJ24 (F8V) substitution, polymorphisms in langerin (CD207 N288D and K313I), as well as variants in CTSC (I453L) and PRF1 (A91V); the last two are known hypomorphs involved in autosomal recessive conditions with abnormal sensitivity to viral infections. This evidence concerns the gene CD207 and viral infectious disease.