Protective immune responses to the 42-kilodalton (kDa) region of Plasmodium yoelii merozoite surface protein 1 are induced by the C-terminal 19-kDa region but not by the adjacent 33-kDa region

被引:36
作者
Ahlborg, N
Ling, IT
Howard, W
Holder, AA
Riley, EM
机构
[1] Univ Edinburgh, Inst Cell Anim & Populat Biol, Edinburgh EH9 3JT, Midlothian, Scotland
[2] Natl Inst Med Res, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
D O I
10.1128/IAI.70.2.820-825.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vaccination of mice with the 42-kDa region of Plasmodium yoelii merozoite surface protein 1 (MSP1(42)) or its 19-kDa C-terminal processing product (MSP1(19)) can elicit protective antibody responses in mice. To investigate if the 33-kDa N-terminal fragment (MSP1(33)) of MSP1(42) also induces protection, the gene segment encoding MSP1(33) was expressed as a glutathione S-transferase (GST) fusion protein. C57BL/6 and BALB/c mice were immunized with GST-MSP1(33) and subsequently challenged with the lethal P. yoelii YM blood stage parasite. GST-MSP1(33) failed to induce protection, and all mice developed patent parasitemia at a level similar to that in naive or control (GST-immunized) mice; mice immunized with GST-MSP1(19) were protected, as has been shown previously. Specific prechallenge immunoglobulin G (IgG) antibody responses to MSPI were analyzed by enzyme-linked immunosorbent assay and immunofluorescence. Despite being unprotected, several mice immunized with MSP1(33) had antibody titers (of all IgG subclasses) that were comparable to or higher than those in mice that were protected following immunization with MSP1(19). The finding that P. yoelii MSP1(33) elicits strong but nonprotective antibody responses may have implications for the design of vaccines for humans based on Plasmodium falciparum or Plasmodium vivax MSP1(42).
引用
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页码:820 / 825
页数:6
相关论文
共 38 条
[1]   Linkage of exogenous T-cell epitopes to the 19-kilodalton region of Plasmodium yoelii merozoite surface protein 1 (MSP119) can enhance protective immunity against malaria and modulate the immunoglobulin subclass response to MSP119 [J].
Ahlborg, N ;
Ling, IT ;
Holder, AA ;
Riley, EM .
INFECTION AND IMMUNITY, 2000, 68 (04) :2102-2109
[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]   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
[6]   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
[7]  
DALY TM, 1995, J IMMUNOL, V155, P236
[8]   A RECOMBINANT 15-KILODALTON CARBOXYL-TERMINAL FRAGMENT OF PLASMODIUM-YOELII-YOELII 17XL MEROZOITE SURFACE PROTEIN-1 INDUCES A PROTECTIVE IMMUNE-RESPONSE IN MICE [J].
DALY, TM ;
LONG, CA .
INFECTION AND IMMUNITY, 1993, 61 (06) :2462-2467
[9]   Levels of antibody to conserved parts of Plasmodium falciparum merozoite surface protein 1 in Ghanaian children are not associated with protection from clinical malaria [J].
Dodoo, D ;
Theander, TG ;
Kurtzhals, JAL ;
Koram, K ;
Riley, E ;
Akanmori, BD ;
Nkrumah, FK ;
Hviid, L .
INFECTION AND IMMUNITY, 1999, 67 (05) :2131-2137
[10]   Characterization of human T- and B-cell epitopes in the C terminus of Plasmodium falciparum merozoite surface protein 1: Evidence for poor T-cell recognition of polypeptides with numerous disulfide bonds [J].
Egan, A ;
Waterfall, M ;
Pinder, M ;
Holder, A ;
Riley, E .
INFECTION AND IMMUNITY, 1997, 65 (08) :3024-3031