Levels of antibody to conserved parts of Plasmodium falciparum merozoite surface protein 1 in Ghanaian children are not associated with protection from clinical malaria

D Dodoo; T G Theander; J A Kurtzhals; K Koram; E Riley; B D Akanmori; F K Nkrumah; L Hviid

Levels of antibody to conserved parts of Plasmodium falciparum merozoite surface protein 1 in Ghanaian children are not associated with protection from clinical malaria

D Dodoo, T G Theander, J A Kurtzhals, K Koram, E Riley, B D Akanmori, F K Nkrumah, L Hviid

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

111 Citationer (Scopus)

Abstract

Udgivelsesdato: 1999-May

Originalsprog	Engelsk
Tidsskrift	Infection and Immunity
Vol/bind	67
Udgave nummer	5
Sider (fra-til)	2131-7
Antal sider	6
ISSN	0019-9567
Status	Udgivet - 1999

Bibliografisk note

Keywords: Adolescent; Animals; Antibodies, Protozoan; Antibody Specificity; Child; Child, Preschool; Conserved Sequence; Female; Ghana; Humans; Immunoglobulin G; Malaria, Falciparum; Male; Merozoite Surface Protein 1; Peptide Fragments; Plasmodium falciparum; Recombinant Fusion Proteins

Citationsformater

@article{d4aef930a06911dd86a6000ea68e967b,

title = "Levels of antibody to conserved parts of Plasmodium falciparum merozoite surface protein 1 in Ghanaian children are not associated with protection from clinical malaria",

abstract = "The 19-kDa conserved C-terminal part of the Plasmodium falciparum merozoite surface protein 1 (PfMSP119) is a malaria vaccine candidate antigen, and human antibody responses to PfMSP119 have been associated with protection against clinical malaria. In this longitudinal study carried out in an area of stable but seasonal malaria transmission with an estimated parasite inoculation of about 20 infective bites/year, we monitored 266 3- to 15-year-old Ghanaian children clinically and parasitologically over a period of 18 months. Blood samples were collected at the beginning of the study before the major malaria season in April and after the season in November. Using enzyme-linked immunosorbent assay, we measured antibody responses to recombinant gluthathione S-transferase-PfMSP119 fusion proteins corresponding to the Wellcome and MAD20 allelic variants in these samples. Prevalence of antibodies recognizing the Wellcome 19 construct containing both epidermal growth factor (EGF)-like motifs in Wellcome type PfMSP119 was about 30%. Prevalence of antibodies to constructs containing only the first EGF domain from either Wellcome or MAD20 type PfMSP119 was about 15%, whereas antibodies recognizing a construct containing only the second EGF domain of MAD20 type PfMSP119 was found in only about 4% of the donors. Neither the prevalence nor the levels of any of the antibody specificities varied significantly with season, age, or sex. Significantly, and in contrast to previous reports from other parts of West Africa, we found no evidence of an association between antibody responses to PfMSP119 and clinical protection against malaria.",

author = "D Dodoo and Theander, {T G} and Kurtzhals, {J A} and K Koram and E Riley and Akanmori, {B D} and Nkrumah, {F K} and L Hviid",

note = "Keywords: Adolescent; Animals; Antibodies, Protozoan; Antibody Specificity; Child; Child, Preschool; Conserved Sequence; Female; Ghana; Humans; Immunoglobulin G; Malaria, Falciparum; Male; Merozoite Surface Protein 1; Peptide Fragments; Plasmodium falciparum; Recombinant Fusion Proteins",

year = "1999",

language = "English",

volume = "67",

pages = "2131--7",

journal = "Infection and Immunity",

issn = "0019-9567",

publisher = "American Society for Microbiology",

number = "5",

}

TY - JOUR

T1 - Levels of antibody to conserved parts of Plasmodium falciparum merozoite surface protein 1 in Ghanaian children are not associated with protection from clinical malaria

AU - Dodoo, D

AU - Theander, T G

AU - Kurtzhals, J A

AU - Koram, K

AU - Riley, E

AU - Akanmori, B D

AU - Nkrumah, F K

AU - Hviid, L

N1 - Keywords: Adolescent; Animals; Antibodies, Protozoan; Antibody Specificity; Child; Child, Preschool; Conserved Sequence; Female; Ghana; Humans; Immunoglobulin G; Malaria, Falciparum; Male; Merozoite Surface Protein 1; Peptide Fragments; Plasmodium falciparum; Recombinant Fusion Proteins

PY - 1999

Y1 - 1999

N2 - The 19-kDa conserved C-terminal part of the Plasmodium falciparum merozoite surface protein 1 (PfMSP119) is a malaria vaccine candidate antigen, and human antibody responses to PfMSP119 have been associated with protection against clinical malaria. In this longitudinal study carried out in an area of stable but seasonal malaria transmission with an estimated parasite inoculation of about 20 infective bites/year, we monitored 266 3- to 15-year-old Ghanaian children clinically and parasitologically over a period of 18 months. Blood samples were collected at the beginning of the study before the major malaria season in April and after the season in November. Using enzyme-linked immunosorbent assay, we measured antibody responses to recombinant gluthathione S-transferase-PfMSP119 fusion proteins corresponding to the Wellcome and MAD20 allelic variants in these samples. Prevalence of antibodies recognizing the Wellcome 19 construct containing both epidermal growth factor (EGF)-like motifs in Wellcome type PfMSP119 was about 30%. Prevalence of antibodies to constructs containing only the first EGF domain from either Wellcome or MAD20 type PfMSP119 was about 15%, whereas antibodies recognizing a construct containing only the second EGF domain of MAD20 type PfMSP119 was found in only about 4% of the donors. Neither the prevalence nor the levels of any of the antibody specificities varied significantly with season, age, or sex. Significantly, and in contrast to previous reports from other parts of West Africa, we found no evidence of an association between antibody responses to PfMSP119 and clinical protection against malaria.

AB - The 19-kDa conserved C-terminal part of the Plasmodium falciparum merozoite surface protein 1 (PfMSP119) is a malaria vaccine candidate antigen, and human antibody responses to PfMSP119 have been associated with protection against clinical malaria. In this longitudinal study carried out in an area of stable but seasonal malaria transmission with an estimated parasite inoculation of about 20 infective bites/year, we monitored 266 3- to 15-year-old Ghanaian children clinically and parasitologically over a period of 18 months. Blood samples were collected at the beginning of the study before the major malaria season in April and after the season in November. Using enzyme-linked immunosorbent assay, we measured antibody responses to recombinant gluthathione S-transferase-PfMSP119 fusion proteins corresponding to the Wellcome and MAD20 allelic variants in these samples. Prevalence of antibodies recognizing the Wellcome 19 construct containing both epidermal growth factor (EGF)-like motifs in Wellcome type PfMSP119 was about 30%. Prevalence of antibodies to constructs containing only the first EGF domain from either Wellcome or MAD20 type PfMSP119 was about 15%, whereas antibodies recognizing a construct containing only the second EGF domain of MAD20 type PfMSP119 was found in only about 4% of the donors. Neither the prevalence nor the levels of any of the antibody specificities varied significantly with season, age, or sex. Significantly, and in contrast to previous reports from other parts of West Africa, we found no evidence of an association between antibody responses to PfMSP119 and clinical protection against malaria.

M3 - Journal article

C2 - 10225865

SN - 0019-9567

VL - 67

SP - 2131

EP - 2137

JO - Infection and Immunity

JF - Infection and Immunity

IS - 5

ER -