Analysis of a Multi-component Multi-stage Malaria Vaccine Candidate-Tackling the Cocktail Challenge

被引:34
作者
Boes, Alexander [1 ]
Spiegel, Holger [1 ]
Voepel, Nadja [1 ]
Edgue, Gueven [1 ]
Beiss, Veronique [1 ]
Kapelski, Stephanie [1 ]
Fendel, Rolf [1 ,2 ]
Scheuermayer, Matthias [3 ]
Pradel, Gabriele [2 ]
Bolscher, Judith M. [4 ]
Behet, Marije C. [5 ]
Dechering, Koen J. [4 ]
Hermsen, Cornelus C. [5 ]
Sauerwein, Robert W. [4 ,5 ]
Schillberg, Stefan [1 ]
Reimann, Andreas [1 ]
Fischer, Rainer [1 ,2 ]
机构
[1] Fraunhofer Inst Mol Biol & Appl Ecol IME, Aachen, Germany
[2] Rhein Westfal TH Aachen, Inst Mol Biotechnol, Aachen, Germany
[3] Zentrum Infekt Forsch, Wurzburg, Germany
[4] TropIQ Hlth Sci, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands
关键词
APICAL MEMBRANE ANTIGEN-1; MEROZOITE SURFACE PROTEIN-3; PLASMODIUM-FALCIPARUM; IMMUNOGENICITY; TRANSMISSION; ANTIBODIES; STAGE; GROWTH; PROTECTION; PARASITE;
D O I
10.1371/journal.pone.0131456
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Combining key antigens from the different stages of the P. falciparum life cycle in the context of a multi-stage-specific cocktail offers a promising approach towards the development of a malaria vaccine ideally capable of preventing initial infection, the clinical manifestation as well as the transmission of the disease. To investigate the potential of such an approach we combined proteins and domains (11 in total) from the pre-erythrocytic, blood and sexual stages of P. falciparum into a cocktail of four different components recombinantly produced in plants. After immunization of rabbits we determined the domain-specific antibody titers as well as component-specific antibody concentrations and correlated them with stage specific in vitro efficacy. Using purified rabbit immune IgG we observed strong inhibition in functional in vitro assays addressing the pre-erythrocytic (up to 80%), blood (up to 90%) and sexual parasite stages (100%). Based on the component-specific antibody concentrations we calculated the IC50 values for the pre-erythrocytic stage (17-25 mu g/ml), the blood stage (4060 mu g/ml) and the sexual stage (1.75 mu g/ml). While the results underline the feasibility of a multi-stage vaccine cocktail, the analysis of component-specific efficacy indicates significant differences in IC50 requirements for stage-specific antibody concentrations providing valuable insights into this complex scenario and will thereby improve future approaches towards malaria vaccine cocktail development regarding the selection of suitable antigens and the ratios of components, to fine tune overall and stage-specific efficacy.
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页数:20
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