Development and pre-clinical analysis of a Plasmodium falciparum Merozoite Surface Protein-142 malaria vaccine

被引:82
作者
Angov, E
Aufiero, BM
Turgeon, AM
Van Handenhove, M
Ockenhouse, CF
Kester, KE
Walsh, DS
McBride, JS
Dubois, MC
Cohen, J
Haynes, JD
Eckels, KH
Heppner, DG
Ballou, WR
Diggs, CL
Lyon, JA
机构
[1] WRAIR, Dept Immunol, Silver Spring, MD 20910 USA
[2] GlaxoSmithKline Biol, Rixensart, Belgium
[3] AFRIMS, Bangkok, Thailand
[4] Univ Edinburgh, Edinburgh, Midlothian, Scotland
[5] WRAIR, Dept Biol Res, Pilot Bioprod Facil, Silver Spring, MD 20910 USA
[6] USAID, Washington, DC USA
关键词
malaria; falciparum; erythrocyte; vaccine; process development; safety; immunogenicity; AS02A; adjuvant; alum; Merozoite Surface Protein-1; MSP-1; growth inhibition; processing inhibition; protein; purification;
D O I
10.1016/S0166-6851(03)00077-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Merozoite Surface Protein-1(42) (MSP-1(42)) is a leading vaccine candidate against erythrocytic malaria parasites. We cloned and expressed Plasmodium falciparum MSP-1(42) (3D7 clone) in Escherichia coli. The antigen was purified to greater than 95% homogeneity by using nickel-, Q- and carboxy-methyl (CM)-substituted resins. The final product, designated Falciparum Merozoite Protein-1 (FMP1), had endotoxin levels significantly lower than FDA standards. It was structurally correct based on binding conformation-dependent mAbs, and was stable. Functional antibodies from rabbits vaccinated with FMP1 in Freund's adjuvant inhibited parasite growth in vitro and also inhibited secondary processing Of MSP-1(42). FMP1 formulated with GlaxoSmithKline Biologicals (GSK) adjuvant, AS02A or alum was safe and immunogenic in rhesus (Macaca mulatta) monkeys. Published by Elsevier Science B.V.
引用
收藏
页码:195 / 204
页数:10
相关论文
共 40 条