Prime-boost with Chikungunya virus E2 envelope protein combined with Poly (I:C) induces specific humoral and cellular immune responses

Abstract

Chikungunya virus (CHIKV) is an arbovirus transmitted to humans mainly by the bite of infected <i>Aedes aegypti</i> and <i>Aedes albopictus</i> mosquitoes. CHIKV illness is characterized by fever and long-lasting arthritic symptoms, and in some cases it is a deadly disease. The CHIKV envelope E2 (E2_CHIKV) glycoprotein is crucial for virus attachment to the cell. Furthermore, E2_CHIKV is the immunodominant protein and the main target of neutralizing antibodies. To date, there is no available prophylactic vaccine or specific treatment against CHIKV infection. Here, we designed and produced a DNA vaccine and a recombinant protein containing a consensus sequence of E2_CHIKV. C57BL/6 mice immunized twice with the E2_CHIKV recombinant protein in the presence of the adjuvant Poly (I:C) induced the highest E2_CHIKV-specific humoral and cellular immune responses, while the immunization with the homologous DNA vaccine pVAX-E2_CHIKV was able to induce specific IFN-γ producing cells. The heterologous prime-boost strategy was also able to induce specific cellular and humoral immune responses that were, in general, lower than the responses induced by the homologous E2_CHIKV recombinant protein immunization. Furthermore, recombinant E2_CHIKV induced the highest titers of neutralizing antibodies. Collectively, we believe this is the first report to analyze E2_CHIKV-specific humoral and cellular immune responses after immunization with E2_CHIKV recombinant protein and DNA pVAX-E2_CHIKV vaccine platforms.