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. 2015 Jan 20;6(1):e02227-14. doi: 10.1128/mBio.02227-14

TABLE 1 .

Summary of binding and postexposure efficacy data available for EBOV therapeuticsa

Candidate therapeutic component Treatment modality Therapeutic(s) Nucleotide position based on GenBank/RefSeq entryb Amino acid residues of target protein Target gene Treatment time p.i. Treatment success (% survival range) Reference(s)
EK-1-mod siRNA Tekmira 17,396–17,418 NA L 30 min to 6 days 66.7–100c 8
VP24-1160-mod siRNA Tekmira 11,043–11,065 NA VP24 30 min to 6 days 66.7–100c 8
VP35-855-mod siRNA Tekmira 3884–3906 NA VP35 30 min to 6 days 66.7–100c 8
1H3 Mab Passive immunization ZMAB 6039–6508 1–157 GP 3–9 days 50–100d 10, 18
2G4 Mab Passive immunization ZMAPP, ZMAB 7540–8039 501–676 GP 3–9 days 50–100d,e 10, 12, 18
4G7 Mab Passive immunization ZMAPP, ZMAB 7414–7542 459–501 GP 3–9 days, 5 days 50–100d,e 10, 12, 18
13C6 Mab Passive immunization MB-003, ZMAPP 6039–7542 1–501 GPf 1–2 days, 5 days 66.7–100e 11, 12, 18, 19
6D8 Mab Passive immunization MB-003 7204–7254 389–405 GP 1–2 days 66.7 11, 19
13F6 Mab Passive immunization MB-003 7240–7290 401–417 GP 1–2 days 66.7 11, 19
AVI-7537 PMO AVI-6002 10,331–10,349 NA VP24 30–60 min 60 9, 15
AVI-7539 PMO AVI-6002 3133–3152 NA VP35 30–60 min 60 9, 15
a

MAb, monoclonal antibody; NA, not applicable; p.i., postinoculation; PMO, phosphorodiamidate morpholino oligomers; siRNA, small interfering RNA. Recognition sequences for PMO and siRNA are listed in the supplemental methods.

b

siRNA positions include both sense and antisense oligonucleotide positions. Mutations specific to each are designated in Fig. 1.

c

Survival range is dependent on dosing.

d

Survival range is dependent on addition of Ad-IFN (interferon co-treatment) to treatment 1 day p.i.

e

Survival range is dependent on formulation.

f

Cross-reacts with TAFV (Tai Forest virus) and SUDV (Sudan virus) GP.