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. 2007 Jun;121(2):158–165. doi: 10.1111/j.1365-2567.2006.02552.x

Table 1.

Immunogenicity and protective efficacy against malaria sporozoite challenge from representative studies carried out in our laboratory

Vaccination regime

Mouse Human


DF DM FM MF AM1 D(D)DM FFM
IFN-γ spot-forming cells/106 spleen cells (mouse) or PBMC (human) 750 1200 3200 3100 1500 1200 CD4 400–500 CD4/CD8
Percentage of individuals protected from challenge with sporozoites 12·5 17·5 67·5 37·5 100
Percentage reduction in infected liver cells 80 92

Mouse results (refs 52, 53)and human data (refs 5456) have been previously described in detail.

1

Separate study.

A, adenovirus priming; D, DNA priming; F, FP9 priming; IFN-γ, interferon-γ; M, modified vaccinia Ankara (MVA) boosting; PBMC, peripheral blood mononuclear cells.

Priming was multiple in the human studies.