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. Author manuscript; available in PMC: 2021 Jun 17.
Published in final edited form as: Curr Issues Mol Biol. 2020 Sep 23;41:469–508. doi: 10.21775/cimb.041.469

Table 2.

HSV-2 vaccine candidates in preclinical development

Candidate Platform Antigenic
Targets
Immune
Response
Results in animal models
THV Trivalent subunit gD, gC, gE Neutralizing Abs Prophylactic in mice and guinea pigs Decreased shedding in guinea pigs
ΔgD-2 gD null Single cycle Multiple targets excluding gD FcγR-activating Abs CD4, CD8 responses Passive protection 100% protection against HSV-1 and HSV-2 clinical isolates in male and female mice with multiple challenge routes; Prevents establishment of latency Passive protection
gD27 gD-nectin binding impaired; Live attenuated Multiple Neutralizing Abs Improved protection compared to gD-2 subunit
VC2 Deleted in gK and UL20 Defective in establishing latency; replication competent Multiple Neutralizing Abs T cell memory (gB, gD) TFH and Th17 responses 100% protection in mice intravaginally challenged with HSV-1(McKrae) or HSV-2(G) Prevents latency