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. Author manuscript; available in PMC: 2021 Jun 1.
Published in final edited form as: Transl Res. 2020 Mar 16;220:138–152. doi: 10.1016/j.trsl.2020.03.004

Table 3.

Prophylactic genital herpes vaccines in preclinical testing

Vaccine candidates Properties References
Live attenuated virus
HSV529* Deletion of two genes essential for replication, UL5, UL29 [113]
HSV-2-ΔgD Emphasis on inducing potent ADCC [85]
HSV-1 VC2 mutations in gK and UL20 Defective in virus entry and retrograde neuronal transport [114]
HSV-2 UL24 mutant Syncytial mutant with reduced virulence [115]
HSV-2 ICP0 mutant Replication-defective [116]
HSV-2gD27 Defective in entry in neuronal cells [44]
Inactivated virus
HSV-2 with MPL/alum Formalin-inactivated virus with adjuvant [117]
Subunit protein antigens
gD2, UL19 and UL25 with GLA-SE adjuvant* Induces potent CD4 and CD8 T cells [42]
HSV-2 gB2, gD2 and UL40 with adjuvants Stimulates potent neutralizing and CD8 T cell responses [64]
gB2 and gD2 in nanoemulsion Intranasal vaccine to block virus entry [118]
Nucleoside-modified mRNA
gC2, gD2, gE2 mRNA-LNP Induces neutralizing antibodies and antibodies that block immune evasion [58]
DNA vaccine
gB2 with chemokine CCL19 Enhanced mucosal antibody response [119]
*

HSV529 is in phase 1/2a human trials as a therapeutic vaccine combined with gD2, UL19 and UL25 and GLA-SE adjuvant (https://clinicaltrials.gov/ct2/show/NCT04222985)