Examples of preclinical studies and clinical trials on vaccines developed for infectious diseases
Disease | Vector | Findings |
---|---|---|
CHIKV | MV-CHIKV | Protection against CHIKV challenges in macaques [63] |
MV-CHIKV | Seroconversion in 100% of volunteers in phase I [64] | |
MV-CHIKV | Good safety, and strong immune responses in phase II [65] | |
EVD | VSV-EBOV-GP | Protection against two EBOV strains in macaques [66, 67] |
VSV-EBOV-GP | Good safety and tolerability in phase I volunteers [68] | |
VSV-ZEBOV | High vaccine efficacy, and protection in phase III [69] | |
VSV-ZEBOV | High vaccine efficacy in phase III volunteers [70] | |
VSV-ZEBOV | Approval of ERVEBO® by the FDA and EMA [71] | |
ZIKV | MV-ZIKV-E | ZIKV-specific Abs, protection against ZIKV of mice fetus [72] |
MV-ZIKV-E | Despite the completion of phase I, no results are available [73] | |
MV-ZIKV-RSP-E | Phase I study in progress [75] | |
MV (TMV-083) | Th1-biased Ab and T cell responses in mice [76] | |
MV (TMV-083) | Weak immune responses, phase I trial discontinued [77, 78] | |
COVID-19 | VSV-SARS-CoV-2 S | Protection against SARS-CoV-2 challenges in mice [79] |
VSV (V590) | Weak immune responses, phase I trial discontinued [80, 81] | |
VSVΔG-SARS-CoV-2 S | Protection against SARS-CoV-2 in hamsters [82] | |
VSVΔG-SARS-CoV-2 S | Phase I/II study in progress [83] | |
LNP-nCoVsaRNA | Strong SARS-CoV-2 specific Ab responses in mice [86] | |
LNP-nCoVsaRNA | Safe but not 100% seroconversion in phase I [87] |
Ab: antibody; CHIKV: chikungunya virus; EBOV-GP: Ebola virus-glycoprotein; EMA: European Medicines Agency; EVD: Ebola virus disease; FDA: US Food and Drug Administration; LNP: lipid nanoparticle; LNP-nCoVsaRNA: LNP-VEE-SARS-CoV-2 S RNA; SARS-CoV-2 S: SARS-CoV-2 spike; ZEBOV: EBOV-Zaire strain
KL is the sole author of the manuscript and contributed to: Conceptualization, Writing—original draft, Writing—review & editing.
The author declares that he has no conflicts of interest.
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© The Author(s) 2023.