Journal
VIRUSES-BASEL
Volume 15, Issue 1, Pages -Publisher
MDPI
DOI: 10.3390/v15010219
Keywords
HSV-2; recombinant adenovirus; therapeutic vaccine
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This study evaluated three recombinant vaccines as therapeutic vaccines against acute and recurrent genital herpes. The rAd-gD2 Delta UL25 vaccine induced a higher titer of binding antibody, while the rAd-gD2 + rAd-Delta UL25 vaccine induced a higher titer of neutralizing antibody. Both vaccines significantly improved survival rates and reduced viral replication.
Genital herpes (GH) has become one of the most common sexually transmitted diseases worldwide, and it is spreading rapidly in developing countries. Approximately 90% of GH cases are caused by HSV-2. Therapeutic HSV-2 vaccines are intended for people already infected with HSV-2 with the goal of reducing clinical recurrences and recurrent virus shedding. In our previous work, we evaluated recombinant adenovirus-based vaccines, including rAd-gD2 Delta UL25, rAd-Delta UL25, and rAd-gD2, for their potency as prophylactic vaccines. In this study, we evaluated these three vaccines as therapeutic vaccines against acute and recurrent diseases in intravaginal challenged guinea pigs. Compared with the control groups, the recombinant vaccine rAd-gD2 Delta UL25 induced a higher titer of the binding antibody, and rAd-gD2 + rAd-Delta UL25 induced a higher titer of the neutralizing antibody. Both rAd-gD2 Delta UL25 and rAd-gD2 + rAd-Delta UL25 vaccines significantly enhanced the survival rate by 50% compared to rAd-gD2 and reduced viral replication in the genital tract and recurrent genital skin disease. Our findings provide a new perspective for HSV-2 therapeutic vaccine research and provide a new technique to curtail the increasing spread of HSV-2.
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