Phase Ia clinical evaluation of the safety and immunogenicity of the Plasmodium falciparum blood-stage antigen AMA1 in ChAd63 and MVA vaccine vectors

Sheehy, SH; Duncan, CJA; Elias, SC; Biswas, S; Collins, KA; O'hara, G; Halstead, FD; Ewer, KJ; Mahungu, T; Spencer, AJ; Miura, K; Poulton, ID; Dicks, MDJ; Edwards, NJ; Berrie, E; Moyle, S; Colloca, S; Cortese, R; Gantlett, K; Long, CA; Lawrie, AM; Gilbert, SC; Doherty, T; Nicosia, A; Hill, AVS and Draper, SJ (2012). Phase Ia clinical evaluation of the safety and immunogenicity of the Plasmodium falciparum blood-stage antigen AMA1 in ChAd63 and MVA vaccine vectors. [Dataset]. London School of Hygiene & Tropical Medicine, London, United Kingdom. 10.17037/DATA.24.
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Traditionally, vaccine development against the blood-stage of Plasmodium falciparum infection has focused on recombinant protein-adjuvant formulations in order to induce high-titer growth-inhibitory antibody responses. However, to date no such vaccine encoding a blood-stage antigen(s) alone has induced significant protective efficacy against erythrocytic-stage infection in a pre-specified primary endpoint of a Phase IIa/b clinical trial designed to assess vaccine efficacy. Cell-mediated responses, acting in conjunction with functional antibodies, may be necessary for immunity against blood-stage P. falciparum. The development of a vaccine that could induce both cell-mediated and humoral immune responses would enable important proof-of-concept efficacy studies to be undertaken to address this question.

Keywords

Vaccines; Enzyme-linked immunoassays; Immune response; Antibodies; Antigens; Cytotoxic T cells; Antibody response

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