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. 2021 Sep 9;9(9):1004. doi: 10.3390/vaccines9091004

Table 1.

DNA vaccines against ZIKV infection.

Vaccine’s Name or Component Immunogenicity in the Induction of Immune Responses Animal Model Vaccine Doses Administration Route Virus Challenged Ref.
prM and E Completely protected mice against ZIKV-associated damage to the testes and sperm and prevented viral persistence in the testes Type-I interferon knockout mice Two doses at two-week interval i.m. Puerto Rico Strain PRVABC59 [17]
pVAX1-ZME (prM and E) Induced robust ZIKV-specific cellular and long-term humoral immune responses with high and sustained neutralizing activity, which provided passive protection against ZIKV infection in neonatal mice BALB/c mice Three doses at three-week intervals i.m. (SMGC-1 strain, GenBank accession number:
KX266255
[18]
GLS-5700 (prM and E) Prevented fertility loss in male IFNAR−/− mice C57BL/6J mice and IFNAR−/− mice Two doses at two-week interval i.m. Puerto Rico Strain PRVABC59 [19]
VRC5288 and VRC5283 Induced detectable T-cell response and antibody response with neutralization activity. The immunogenicity of VRC5283 was better than that of VRC5288. Humans Single dose, two and three doses i.m No [20]
prM and E Elicited protective responses against multiple diverse ZIKV isolates C57BL/6c mice Four doses at days 0, 24, 42, and 199 i.m Puerto Rico Strain PRVABC59 [21]
pVAX-NS1, pVAX-tpaNS1, pVAX-tpaNS1-IMX313P (NS1) pVAX-tpaNS1 vaccination induced significantly higher NS1-specific antibody titers and CD4+, as well as CD8+, T-cell responses compared to pVAX-NS1 and pVAX-tpaNS1- IMX313P BALB/c and IFNAR−/− mice Three doses at two-week intervals i.d. ZIKVzkv2015 [22]

Note: prM, anterior membrane; E, envelope; IFNAR−/−, type I IFN receptor–deficient; i.m., intramuscular injection; i.d., intradermal injection.