Table 1.
Name | Platform | Antigens | Immune Response |
Clinical Results |
---|---|---|---|---|
gB/gD/MF59 (Chiron) | Subunit MF59 adjuvant | gD and gB | Neutralizing Abs | Phase 3 Prophylaxis 9% (95% CI: −29%, 36%) |
gD/AS04 (GSK) | Subunit AS04 adjuvant | gD | Neutralizing Abs CD4+ T cells | Phase 3 Prophylaxis 20% (95% CI: −29%, 50%) |
gH-null (Cantab Pharmaceuticals) | Single-cycle live | Multiple | Neutralizing Abs | Phase 3 therapeutic No difference in recurrences or shedding |
HSV529 (Sanofi-Pasteur) | Replication-defective | Multiple | Neutralizing Abs CD4, CD8 T cells | Phase 1 Safe but immunogenic in doubly-seronegatives only |
Gen-003 (Genocea) | Subunit Saponin adjuvant | gD, ICP4 | Neutralizing Abs Cytolytic T cells | Phase 2 therapeutic Dose variable decrease shedding |
HerpV (Agenus) | Heat shock protein 70-HSV peptides QS-21 adjuvant | 32 HSV peptides (gD, additional envelope, tegument, and other) | Cytotoxic T cells | Phase 2 therapeutic 17% reduction in shedding frequency |
Vaxfectin (Vical) | DNA Vaxfectin adjuvant | gD, UL46/47 | Neutralizing Abs | Phase 1/2 therapeutic Failed to reduce shedding |
COR-1 (Admedus) | Codon optimized DNA | Codon optimized gD2 and ubiquitin-fused truncated gD2 to target the antigen to the proteasome | gD-specific Abs Cytotoxic T cells | Phase 2 therapeutic No difference in recurrences |
ΔNLS (Rational Vaccines) | Deleted in ICP0 Replication competent Attenuated for latency | Multiple targets | Neutralizing Abs gD-specific Abs | Phase 1 non-FDA approved therapeutic study Self-reported reduction in recurrences |