Live Attenuated Tetravalent Dengue Virus Host Range Vaccine Is Immunogenic in African Green Monkeys following a Single

The causative agent of dengue fever, dengue virus (DENV), is transmitted by mosquitoes, and as distribution of these insects has expanded, so has dengue-related disease. DENV is a member of the Flaviviridae family and has 4 distinct serotypes (DENV-1,-2,-3, and-4). No lasting cross protection is afforded to heterologous serotypes following infection by any one of the individual se-rotypes. The presence of nonneutralizing antibodies to one serotype can facilitate the occurrence of more-severe dengue hemor-rhagic fever through immune enhancement upon infection with a second serotype. For this reason, the development of a safe, tetravalent vaccine to produce a balanced immune response to all four serotypes is critical. We have developed a novel approach to produce safe and effective live-attenuated vaccines for DENV and other insect-borne viruses. Host range (HR) mutants of each DENV serotype were created by truncating transmembrane domain 1 of the E protein and selecting for strains of DENV that replicated well in insect cells but not mammalian cells. These vaccine strains were tested for immunogenicity in African green monkeys (AGMs). No vaccine-related adverse events occurred. The vaccine strains were confirmed to be attenuated in vivo by infectious center assay (ICA). Analysis by 50 % plaque reduction neutralization test (PRNT50) established that by day 62 postvac-cination, 100 % of animals seroconverted to DENV-1,-2,-3, and-4. Additionally, the DENVHR tetravalent vaccine (HR-Tet) showed a tetravalent anamnestic immune response in 100 % (16/16) of AGMs after challenge with wild-type (WT) DENV strains. IMPORTANCE We have generated a live attenuated viral (LAV) vaccine capable of eliciting a strong immune response in African greenmonkey