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. 2021 Feb 19;11:599568. doi: 10.3389/fimmu.2020.599568

Table 2.

Responses to rVSV-ZEBOV.

Model Responses to rVSV-ZEBOV
Protection? Antibody production? CD4+/CD8+ B cells NK cells
Humans Yes (127). Yes. Antibodies also cross-react with other EBOV species (127). Increased activation of both CD4+ and CD8+ T cells (76). Polyclonal, convergent B cell responses observed in a trial of 4 vaccinees (127). Modulation of NK cells contributes to early efficacy of the vaccine (128).
Macaques (cynomolgus and rhesus) Yes (86) (108) (113). Yes. Strong correlation observed between GP-specific IgG and survival (86) (108) (113). Similar to natural infection, circulating CD4+ and CD8+ T cells declined during infection, regardless of prior treatment or vaccination (86). CD4+ T cells likely contribute to establishing protection from vaccination (109) whilst CD8+ T cells are not required for vaccine protection (101). Required for production of antibodies which mediate protection. Although CD20-depleted macaques were shown to have detectable EBOV-specific antibodies, this is likely due to persistence in lymphoid organs (101). Increased in response to vaccine (86).
African green monkeys ND ND ND ND ND
Mice (mouse-adapted model) Yes (129) (113). Yes. Strong correlation observed between GP-specific IgG and survival (113). CD8+ T cell depletion does not compromise protection (107).
CD4+ T cells (and B cells) are main mediators of protection (112).
B cells (and CD4+ T cells) are the main mediators of protection (112). NK-cell population is enhanced by vaccine and increases survival (130).
Naïve or immunocompromised mice Yes (107). Able to tolerate vaccine (107). NA NA NA
HSC-transfer mice ND ND ND ND ND
Ferret Yes (131). Yes (131). ND ND ND
Guinea pig (guinea-pig adapted model) Yes (112). Yes. Strong correlation observed between GP-specific IgG and survival (112). ND ND ND
Hamster Yes (24). Yes (24). ND ND ND

Protection and adaptive immune responses observed in humans and animal models. NA, Not applicable; ND, Not determined.