RECOMBINANT VACCINIA VIRUSES CO-EXPRESSING DENGUE-1 GLYCOPROTEINS PRMAND E-INDUCE NEUTRALIZING ANTIBODIES IN MICE

Four recombinant vaccinia viruses expressing different portions of the dengue type I virus (DEN-I) genome (C-prM-E-NS1-NS2A-NS2B; prM-E; prM -E-NS1-NS2A-NS2B; or NS1-NS2A) were constructed in order to establish the most immunogenic configuration of DEN-1 proteins. Both recombinant s producing prM and E in the absence of c induced the synthesis of ext racellular forms of E in vitro. Mice inoculated with these two recombi nants produced DEN-I neutralizing (NEUT) and haemagglutination inhibit ing (HAI) antibodies. The other two recombinant vaccinia viruses, whic h did not induce the production of extracellular forms of E, did not i nduce E-specific immune responses. These results support our previous studies on the design of flavivirus-vaccinia vaccine candidates by sho wing the importance of co-expressing prM and E in order to induce the synthesis of extracellular E and to elicit NEUT and HAI antibodies.