Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates

Ayman Khattab; Christina Reinhardt; Trine Staalsoe; Nadine Fievet; Peter G Kremsner; Philippe Deloron; Lars Hviid; Mo-Quen Klinkert

doi:10.1186/1475-2875-3-21

Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates

Ayman Khattab, Christina Reinhardt, Trine Staalsoe, Nadine Fievet, Peter G Kremsner, Philippe Deloron, Lars Hviid, Mo-Quen Klinkert

Centre for Medical Parasitology

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

18 Citationer (Scopus)

Abstract

Udgivelsesdato: 2004-Jul-8

Originalsprog	Engelsk
Tidsskrift	Malaria Journal
Vol/bind	3
Sider (fra-til)	21
ISSN	1475-2875
DOI	https://doi.org/10.1186/1475-2875-3-21
Status	Udgivet - 2004

Bibliografisk note

Keywords: Animals; Antibodies, Protozoan; Antibody Specificity; Chondroitin Sulfates; Cohort Studies; Erythrocytes; Female; Flow Cytometry; Humans; Immunoglobulin G; Malaria, Falciparum; Male; Parasitemia; Parity; Placenta; Plasmodium falciparum; Pregnancy; Pregnancy Complications, Parasitic; Variant Surface Glycoproteins, Trypanosoma

Adgang til dokumentet

10.1186/1475-2875-3-21

Citationsformater

Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates. / Khattab, Ayman; Reinhardt, Christina; Staalsoe, Trine; Fievet, Nadine; Kremsner, Peter G; Deloron, Philippe; Hviid, Lars; Klinkert, Mo-Quen.

I: Malaria Journal, Bind 3, 2004, s. 21.

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

@article{a488b870a03411dd86a6000ea68e967b,

title = "Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates",

abstract = "BACKGROUND: Pregnancy-associated malaria (PAM) is caused by Plasmodium falciparum-infected erythrocytes that can sequester in placental intervillous space by expressing particular variant surface antigens (VSA) that can mediate adhesion to chondroitin sulfate A (CSA) in vitro. IgG antibodies with specificity for the VSA expressed by these parasites (VSAPAM) are associated with protection from maternal anaemia, prematurity and low birth weight, which is the greatest risk factor for death in the first month of life. METHODS: In this study, the development of anti-VSAPAM antibodies in a group of 151 women who presented to the maternity ward of Albert Schweitzer Hospital in Lambar{\'e}n{\'e}, Gabon for delivery was analysed using flow cytometry assays. Plasma samples from placenta infected primiparous women were also investigated for their capacity to inhibit parasite binding to CSA in vitro. RESULTS: In the study cohort, primiparous as well as secundiparous women had the greatest risk of infection at delivery as well as during pregnancy. Primiparous women with infected placentas at delivery showed higher levels of VSAPAM-specific IgG compared to women who had no malaria infections at delivery. Placental isolates of Gabonese and Senegalese origin tested on plasma samples from Gabon showed parity dependency and gender specificity patterns. There was a significant correlation of plasma reactivity as measured by flow cytometry between different placental isolates. In the plasma of infected primiparous women, VSAPAM-specific IgG measured by flow cytometry could be correlated with anti-adhesion antibodies measured by the inhibition of CSA binding. CONCLUSION: Recognition of placental parasites shows a parity- and sex- dependent pattern, like that previously observed in laboratory strains selected to bind to CSA. Placental infections at delivery in primiparous women appear to be sufficient to induce functional antibodies which can both recognize the surface of the infected erythrocytes as well as block their binding to CSA. The correlation between serum reactivities of placental field isolates from different geographic locations and collected at different times is indicative of the conserved nature of the antigen(s) mediating PAM.",

author = "Ayman Khattab and Christina Reinhardt and Trine Staalsoe and Nadine Fievet and Kremsner, {Peter G} and Philippe Deloron and Lars Hviid and Mo-Quen Klinkert",

note = "Keywords: Animals; Antibodies, Protozoan; Antibody Specificity; Chondroitin Sulfates; Cohort Studies; Erythrocytes; Female; Flow Cytometry; Humans; Immunoglobulin G; Malaria, Falciparum; Male; Parasitemia; Parity; Placenta; Plasmodium falciparum; Pregnancy; Pregnancy Complications, Parasitic; Variant Surface Glycoproteins, Trypanosoma",

year = "2004",

doi = "10.1186/1475-2875-3-21",

language = "English",

volume = "3",

pages = "21",

journal = "Malaria Journal",

issn = "1475-2875",

publisher = "BioMed Central",

}

TY - JOUR

T1 - Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates

AU - Khattab, Ayman

AU - Reinhardt, Christina

AU - Staalsoe, Trine

AU - Fievet, Nadine

AU - Kremsner, Peter G

AU - Deloron, Philippe

AU - Hviid, Lars

AU - Klinkert, Mo-Quen

N1 - Keywords: Animals; Antibodies, Protozoan; Antibody Specificity; Chondroitin Sulfates; Cohort Studies; Erythrocytes; Female; Flow Cytometry; Humans; Immunoglobulin G; Malaria, Falciparum; Male; Parasitemia; Parity; Placenta; Plasmodium falciparum; Pregnancy; Pregnancy Complications, Parasitic; Variant Surface Glycoproteins, Trypanosoma

PY - 2004

Y1 - 2004

N2 - BACKGROUND: Pregnancy-associated malaria (PAM) is caused by Plasmodium falciparum-infected erythrocytes that can sequester in placental intervillous space by expressing particular variant surface antigens (VSA) that can mediate adhesion to chondroitin sulfate A (CSA) in vitro. IgG antibodies with specificity for the VSA expressed by these parasites (VSAPAM) are associated with protection from maternal anaemia, prematurity and low birth weight, which is the greatest risk factor for death in the first month of life. METHODS: In this study, the development of anti-VSAPAM antibodies in a group of 151 women who presented to the maternity ward of Albert Schweitzer Hospital in Lambaréné, Gabon for delivery was analysed using flow cytometry assays. Plasma samples from placenta infected primiparous women were also investigated for their capacity to inhibit parasite binding to CSA in vitro. RESULTS: In the study cohort, primiparous as well as secundiparous women had the greatest risk of infection at delivery as well as during pregnancy. Primiparous women with infected placentas at delivery showed higher levels of VSAPAM-specific IgG compared to women who had no malaria infections at delivery. Placental isolates of Gabonese and Senegalese origin tested on plasma samples from Gabon showed parity dependency and gender specificity patterns. There was a significant correlation of plasma reactivity as measured by flow cytometry between different placental isolates. In the plasma of infected primiparous women, VSAPAM-specific IgG measured by flow cytometry could be correlated with anti-adhesion antibodies measured by the inhibition of CSA binding. CONCLUSION: Recognition of placental parasites shows a parity- and sex- dependent pattern, like that previously observed in laboratory strains selected to bind to CSA. Placental infections at delivery in primiparous women appear to be sufficient to induce functional antibodies which can both recognize the surface of the infected erythrocytes as well as block their binding to CSA. The correlation between serum reactivities of placental field isolates from different geographic locations and collected at different times is indicative of the conserved nature of the antigen(s) mediating PAM.

AB - BACKGROUND: Pregnancy-associated malaria (PAM) is caused by Plasmodium falciparum-infected erythrocytes that can sequester in placental intervillous space by expressing particular variant surface antigens (VSA) that can mediate adhesion to chondroitin sulfate A (CSA) in vitro. IgG antibodies with specificity for the VSA expressed by these parasites (VSAPAM) are associated with protection from maternal anaemia, prematurity and low birth weight, which is the greatest risk factor for death in the first month of life. METHODS: In this study, the development of anti-VSAPAM antibodies in a group of 151 women who presented to the maternity ward of Albert Schweitzer Hospital in Lambaréné, Gabon for delivery was analysed using flow cytometry assays. Plasma samples from placenta infected primiparous women were also investigated for their capacity to inhibit parasite binding to CSA in vitro. RESULTS: In the study cohort, primiparous as well as secundiparous women had the greatest risk of infection at delivery as well as during pregnancy. Primiparous women with infected placentas at delivery showed higher levels of VSAPAM-specific IgG compared to women who had no malaria infections at delivery. Placental isolates of Gabonese and Senegalese origin tested on plasma samples from Gabon showed parity dependency and gender specificity patterns. There was a significant correlation of plasma reactivity as measured by flow cytometry between different placental isolates. In the plasma of infected primiparous women, VSAPAM-specific IgG measured by flow cytometry could be correlated with anti-adhesion antibodies measured by the inhibition of CSA binding. CONCLUSION: Recognition of placental parasites shows a parity- and sex- dependent pattern, like that previously observed in laboratory strains selected to bind to CSA. Placental infections at delivery in primiparous women appear to be sufficient to induce functional antibodies which can both recognize the surface of the infected erythrocytes as well as block their binding to CSA. The correlation between serum reactivities of placental field isolates from different geographic locations and collected at different times is indicative of the conserved nature of the antigen(s) mediating PAM.

U2 - 10.1186/1475-2875-3-21

DO - 10.1186/1475-2875-3-21

M3 - Journal article

C2 - 15242514

VL - 3

SP - 21

JO - Malaria Journal

JF - Malaria Journal

SN - 1475-2875

ER -