Immunogenicity and efficacy in Aotus monkeys of four recombinant Plasmodium falciparum vaccines in multiple adjuvant formulations based on the 19-kilodalton C terminus of merozoite surface protein 1

被引:92
作者
Kumar, S
Collins, W
Egan, A
Yadava, A
Garraud, O
Blackman, MJ
Guevara-Patino, JA
Diggs, C
Kaslow, DC
机构
[1] NIH, Parasit Dis Lab, Bethesda, MD 20892 USA
[2] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, Div Parasit Dis, Atlanta, GA 30333 USA
[3] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, Sci Resources Program, Atlanta, GA 30333 USA
[4] Natl Inst Med Res, Div Parasitol, London NW7 1AA, England
[5] US Agcy Int Dev, Malad Vaccine Dev Program, Washington, DC 20523 USA
关键词
D O I
10.1128/IAI.68.4.2215-2223.2000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immunogenicity and protective efficacy of four versions of recombinant C-terminal 19-kDa epidermal growth factor-like region of the major surface protein 1 (rMSP1(19)) of Plasmodium falciparum was studied in Aotus monkeys. Vaccination with each of the four rMSP1(19) constructs elicited high levels of antibodies to MSP1(19) but only one construct, the 19-kDa fragment expressed as a secreted fusion protein from Saccharomyces cerevisiae (yP30P2MSP1(19)), induced a high degree of protective immunity in Aotus nancymai against lethal P. falciparum challenge. Protective formulation required Freund's adjuvant; vaccination with yP30P2MSP1(19) in six other adjuvants that are suitable for human use induced lower levels of antibody response and no protection. These results emphasize the need to continue the search for an adjuvant that is comparable to Freund's adjuvant in potency and is safe for use in humans.
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页码:2215 / 2223
页数:9
相关论文
共 25 条
[1]  
BLACKMAN MJ, 1994, METHOD CELL BIOL, V45, P213
[2]   PROCESSING OF THE PLASMODIUM-FALCIPARUM MAJOR MEROZOITE SURFACE PROTEIN-1 - IDENTIFICATION OF A 33-KILODALTON SECONDARY PROCESSING PRODUCT WHICH IS SHED PRIOR TO ERYTHROCYTE INVASION [J].
BLACKMAN, MJ ;
WHITTLE, H ;
HOLDER, AA .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1991, 49 (01) :35-44
[3]   A SINGLE FRAGMENT OF A MALARIA MEROZOITE SURFACE PROTEIN REMAINS ON THE PARASITE DURING RED-CELL INVASION AND IS THE TARGET OF INVASION-INHIBITING ANTIBODIES [J].
BLACKMAN, MJ ;
HEIDRICH, HG ;
DONACHIE, S ;
MCBRIDE, JS ;
HOLDER, AA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (01) :379-382
[4]   ANTIBODIES INHIBIT THE PROTEASE-MEDIATED PROCESSING OF A MALARIA MEROZOITE SURFACE PROTEIN [J].
BLACKMAN, MJ ;
SCOTTFINNIGAN, TJ ;
SHAI, S ;
HOLDER, AA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :389-393
[5]   EXPRESSION OF THE 19-KILODALTON CARBOXY-TERMINAL FRAGMENT OF THE PLASMODIUM-FALCIPARUM MEROZOITE SURFACE PROTEIN-1 IN ESCHERICHIA-COLI AS A CORRECTLY FOLDED PROTEIN [J].
BURGHAUS, PA ;
HOLDER, AA .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1994, 64 (01) :165-169
[6]   Immunization of Aotus nancymai with recombinant C terminus of Plasmodium falciparum merozoite surface protein 1 in liposomes and alum adjuvant does not induce protection against a challenge infection [J].
Burghaus, PA ;
Wellde, BT ;
Hall, T ;
Richards, RL ;
Egan, AF ;
Riley, EM ;
Ballou, WP ;
Holder, AA .
INFECTION AND IMMUNITY, 1996, 64 (09) :3614-3619
[7]  
BURNS JM, 1989, J IMMUNOL, V143, P2670
[8]   A recombinant Baculovirus 42-kilodalton c-terminal fragment of Plasmodium falciparum merozoite surface protein 1 protects Aotus monkeys against malaria [J].
Chang, SP ;
Case, SE ;
Gosnell, WL ;
Kramer, KJ ;
Tam, LQ ;
Hashiro, CQ ;
Nikaido, CM ;
Gibson, HL ;
LeeNg, CT ;
Barr, PJ ;
Yokota, BT ;
Hui, GSN .
INFECTION AND IMMUNITY, 1996, 64 (01) :253-261
[9]  
CHANG SP, 1992, J IMMUNOL, V149, P548
[10]  
DALY TM, 1995, J IMMUNOL, V155, P236