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Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates
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 sp...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC479693/ https://www.ncbi.nlm.nih.gov/pubmed/15242514 http://dx.doi.org/10.1186/1475-2875-3-21 |
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author | Khattab, Ayman Reinhardt, Christina Staalsoe, Trine Fievet, Nadine Kremsner, Peter G Deloron, Philippe Hviid, Lars Klinkert, Mo-Quen |
author_facet | Khattab, Ayman Reinhardt, Christina Staalsoe, Trine Fievet, Nadine Kremsner, Peter G Deloron, Philippe Hviid, Lars Klinkert, Mo-Quen |
author_sort | Khattab, Ayman |
collection | PubMed |
description | 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 (VSA(PAM)) 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-VSA(PAM )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 VSA(PAM)-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, VSA(PAM)-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. |
format | Text |
id | pubmed-479693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-4796932004-07-22 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 Malar J Research 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 (VSA(PAM)) 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-VSA(PAM )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 VSA(PAM)-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, VSA(PAM)-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. BioMed Central 2004-07-08 /pmc/articles/PMC479693/ /pubmed/15242514 http://dx.doi.org/10.1186/1475-2875-3-21 Text en Copyright © 2004 Khattab et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Khattab, Ayman Reinhardt, Christina Staalsoe, Trine Fievet, Nadine Kremsner, Peter G Deloron, Philippe Hviid, Lars Klinkert, Mo-Quen Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates |
title | Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates |
title_full | Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates |
title_fullStr | Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates |
title_full_unstemmed | Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates |
title_short | Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates |
title_sort | analysis of igg with specificity for variant surface antigens expressed by placental plasmodium falciparum isolates |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC479693/ https://www.ncbi.nlm.nih.gov/pubmed/15242514 http://dx.doi.org/10.1186/1475-2875-3-21 |
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