Table 2.
Efficacy of vaccines in animal models of filovirus infection.
Vaccine | Viral protein including vaccines | Species tested | Strategy | Challenge virus | Survival rate (%) | References | ||
---|---|---|---|---|---|---|---|---|
Dose/Schedule | Route | |||||||
VEEV | MARV Musoke GP or NP | Guinea pig | 106 FFU, 2 or 3 doses | sc | GP-adapted MARV Musoke | 100 | Hevey et al., 1998 | |
MARV Musoke GP or GP + NP | NHP | 107 FFU, 3 doses | MARV Musoke | 100 | ||||
MARV Musoke NP | 67 | |||||||
EBOV NP or GP + NP | Mouse | 2 × 106 IU, 2 doses | mouse-adapted EBOV | 100 | Pushko et al., 2001 | |||
EBOV GP | 90 | |||||||
EBOV GP or GP + NP | Guinea pig | GP-adapted EBOV | 100 | |||||
EBOV NP | 20 | |||||||
EBOV GP, NP or GP + NP | NHP | 107 FFU, 3 doses | EBOV | 0 | Geisbert et al., 2002 | |||
AdV | GPs of MARV (Musoke and Ci67) and RAVV | Guinea pig | 5 × 107−8 PFU, 2 doses | sc | MARV (Musoke or Ci67) or RAVV | 100 | Wang et al., 2006a | |
MARV Angola GP | NHP | 1011 PU, 1dose | im | MARV Angola | 100 | Geisbert et al., 2010a | ||
EBOV GP | Mouse | 108 PFU, 2 doses | sc | mouse-adapted EBOV | 100 | Wang et al., 2006b | ||
EBOV GP + NP | NHP | 2 × 1012 particles, 1 or 2 doses | im | EBOV | 100 | Sullivan et al., 2003 | ||
GPs of EBOV and SUDV, MARV (Musoke and Ci67) and RAVV + NP of EBOV and MARV Musoke | 4 × 1010 PFU, 2 doses | EBOV, SUDV or MARV (Musoke or Ci67) | 100 | Swenson et al., 2008a | ||||
DNA | MARV Musoke or RAVV GP | Guinea pig | 10 μg, 3 or 4 doses with RIBI aadjuvand | sc | GP-adapted MARV Musoke | 100 | Riemenschneider et al., 2003 | |
MARV Musoke GP | NHP | 20 μg, 3 doses | MARV Musoke | 67 | ||||
MARV Angola GP | 4 mg, 4 doses | im | MARV Angola | 100 | Geisbert et al., 2010a | |||
EBOV GP | Mouse | 0.5 μg, 4 doses | mouse-adapted EBOV | 78 | Vanderzanden et al., 1998 | |||
0.5 μg, 1 dose and 1.5 μg, 3 or 4 doses | 100 | |||||||
EBOV GP or NP | Guinea pig | 500 μg, 4 doses | GP-adapted EBOV | 100 | Xu et al., 1998 | |||
DNA + AdV | DNA: GPs of EBOV, SUDV and TAFV + EBOV NP AdV: EBOV GP | NHP | 4 mg of DNA, 3 doses and boosted with 1010 PFU of AdV | im | EBOV | 100 | Sullivan et al., 2000 | |
DNA: MARV Angola GP AdV: MARV Angola GP | 4 mg of DNA, 3 doses and boosted with 1011 PU of AdV | MARV Angola | 100 | Geisbert et al., 2010a | ||||
HPIV3 | EBOV GP or GP + NP | Guinea pig | 105.3 PFU | in | GP-adapted EBOV | 100 | Bukreyev et al., 2006 | |
EBOV GP, GP + NP, or GP + GM-CSF | NHP | 4 × 106 TCID50, 1 dose | in and intracheally | EBOV | 83 | Bukreyev et al., 2007 | ||
EBOV GP | 2 × 107 TCID50, 2 doses | 100 | ||||||
HPIV3/ΔHN-F | EBOV GP | Guinea pig | 4 × 105 PFU, 1 dose | in | GP-adapted EBOV | 100 | Bukreyev et al., 2009 | |
VSV | MARV Musoke GP | NHP | 2 × 107 PFU, 1 dose | 28 day before infection | im | MARV (Musoke or Angola) or RAVV | 100 | Daddario-Dicaprio et al., 2006a |
107 PFU, 1 dose | 28 or 141 d before infectiona | MARV Musoke and Popp | 100 | Jones et al., 2005 | ||||
EBOV GP | Mouse | 2 × 105 PFU, 1 dose | 24 h before infection | ip | mouse-adapted EBOV | 100 | Feldmann et al., 2007 | |
30 mpi | 100 | |||||||
24 hpi | 100 | |||||||
Guinea pig | 24 h before infection | GP-adapted EBOV | 67 | |||||
1 hpi | 83 | |||||||
24 hpi | 50 | |||||||
NHP | 107 PFU, 1 dose | 28 day before infection | im | EBOV | 100 | Jones et al., 2005 | ||
107 PFU, 1 dose | 262 day before infectionb | SUDV | 25 | |||||
EBOV GP + SUDV GP + Musoke GP | 3 × 107 PFU, 1 dose | 28 day before infection | EBOV, SUDV, TAFV or MARV Musoke | 100 | Geisbert et al., 2009 | |||
MARV Musoke GP | 2 × 107 PFU, 1 dose | 24 hpi | MARV Musoke | 83 | Geisbert et al., 2010c | |||
48 hpi | 33 | |||||||
1 × 107 PFU, 1 dose | 20–30 mpi | 100 | Daddario-Dicaprio et al., 2006b | |||||
EBOV GP | 2 × 107 PFU, 1 dose, 20–30 mpi | EBOV | 50 | Feldmann et al., 2007 | ||||
SUDV GP | SUDV | 100 | Geisbert et al., 2008 | |||||
VLP | MARV Musoke GP + VP40 produced in 293Tc | Guinea pig | 50 μg, 3 doses with RIBI adjuvant | im | GP-adapted MARV (Musoke or Ci67) or RAVV | 100 | Swenson et al., 2008b | |
NHP | 1 mg, 3 doses with QS-21 adjuvant | MARV (Musoke or Ci67) or RAVV | 100 | |||||
EBOV GP + VP40 + NP produced in 293Tc | Mouse | 50 μg, 2 doses, with QS-21 adjuvant | Mouse-adapted-EBOV | 100 | Warfield et al., 2007a | |||
EBOV GP + VP40 produced in 293Tc | 10 μg, 3 doses | im or ip | 100 | Warfield et al., 2003 | ||||
EBOV GP + NP + VP40 produced in 293Tc | NHP | 250 μg, 3 doses, with RIBI adjuvant | im | EBOV | 100 | Warfield et al., 2007b | ||
EBOV GP + VP40 produced in insect cellsd | mouse | 50 μg, 2 doses | Mouse-adapted-EBOV | 100 | Sun et al., 2009 | |||
10 μg, 3 doses | 83 | |||||||
EBOV GP + VP40 + NP produced in insect cellsd | 10-50 μg, 2 doses, with QS-21 adjuvant | 100 | Warfield et al., 2007a |
Cynomolgus macaques were immunized by intramuscular injection with a single dose of VSVΔG expressing MARV Musoke GP and subsequently challenged on Day 28 after immunization by intramuscular injection with MARV Musoke strain. The immunized macaques, which were protected from the lethal MARV challenge, were rechallenged with MARV Popp strain 113 days after initial challenge (141 days after immunization).
Cynomolgus macaques were immunized by intramuscular injection with a single dose of VSVΔG expressing EBOV GP and subsequently challenged on Day 28 after immunization by intramuscular injection with EBOV. The macaques protected from the lethal EBOV challenge were rechallenged with SUDV 234 days after initial challenge (262 days after immunization).
293T cells were cotransfected with plasmid vectors encoding GP and VP40 (and NP) of EBOV or MARV. The VLPs were collected and purified from the cell supernatants.
The VLPs were produced by use of recombinant baculovirus constructs expressing GP and VP (and NP) of EBOV or MARV from coinfected insect cells.
Abbreviations
- FFU
focus-forming unit
- GP-adapted
guinea pig-adapted
- IU
infectious unit
- PFU
plaque-forming units
- PU
particle units
- sc
subcutaneously
- im
intramuscularly
- in
intranasally
- ip
intrapenitoneally
- mpi
minutes post-infection
- hpi
hours post-infection
- dpi
days post-infection.