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Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria

Sequestration of Plasmodium falciparum-infected erythrocytes expressing the VAR2CSA antigen in the placenta results in poor pregnancy outcomes, including low birth weight and maternal anemia. Antigen-specific antibody-mediated immunity is acquired during successive pregnancies. Thus, evaluating VAR2...

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Autores principales: Tornyigah, Bernard, d’Almeida, Tania, Escriou, Guillaume, Viwami, Firmine, Fievet, Nadine, Luty, Adrian J. F., Massougbodji, Achille, Nielsen, Morten A., Deloron, Philippe, Tuikue Ndam, Nicaise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099026/
https://www.ncbi.nlm.nih.gov/pubmed/33968015
http://dx.doi.org/10.3389/fimmu.2021.610305
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author Tornyigah, Bernard
d’Almeida, Tania
Escriou, Guillaume
Viwami, Firmine
Fievet, Nadine
Luty, Adrian J. F.
Massougbodji, Achille
Nielsen, Morten A.
Deloron, Philippe
Tuikue Ndam, Nicaise
author_facet Tornyigah, Bernard
d’Almeida, Tania
Escriou, Guillaume
Viwami, Firmine
Fievet, Nadine
Luty, Adrian J. F.
Massougbodji, Achille
Nielsen, Morten A.
Deloron, Philippe
Tuikue Ndam, Nicaise
author_sort Tornyigah, Bernard
collection PubMed
description Sequestration of Plasmodium falciparum-infected erythrocytes expressing the VAR2CSA antigen in the placenta results in poor pregnancy outcomes, including low birth weight and maternal anemia. Antigen-specific antibody-mediated immunity is acquired during successive pregnancies. Thus, evaluating VAR2CSA-specific IgG profiles among pregnant women will increase knowledge on the immunological mechanisms associated with protection, and help in the development of VAR2CSA-based placental malaria vaccines. Using the PAMVAC candidate vaccine antigen, we assessed anti-VAR2CSA IgG subclass responses of a cohort of pregnant Beninese, and analyzed their relationships with pregnancy outcomes. Cytophilic IgG1 and IgG3 responses were the most frequent, with prevalences ranging from 28% (IgG3) up to 50% (IgG1). Elevated levels of VAR2CSA-specific total IgG and cytophilic IgG3 during pregnancy were consistently associated with higher birth weights, whilst high levels of IgG4 were associated with a reduced risk of placental infections. This suggests that protective anti-VAR2CSA IgG responses are coordinated between both cytophilic and non-cytophilic antibodies.
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spelling pubmed-80990262021-05-06 Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria Tornyigah, Bernard d’Almeida, Tania Escriou, Guillaume Viwami, Firmine Fievet, Nadine Luty, Adrian J. F. Massougbodji, Achille Nielsen, Morten A. Deloron, Philippe Tuikue Ndam, Nicaise Front Immunol Immunology Sequestration of Plasmodium falciparum-infected erythrocytes expressing the VAR2CSA antigen in the placenta results in poor pregnancy outcomes, including low birth weight and maternal anemia. Antigen-specific antibody-mediated immunity is acquired during successive pregnancies. Thus, evaluating VAR2CSA-specific IgG profiles among pregnant women will increase knowledge on the immunological mechanisms associated with protection, and help in the development of VAR2CSA-based placental malaria vaccines. Using the PAMVAC candidate vaccine antigen, we assessed anti-VAR2CSA IgG subclass responses of a cohort of pregnant Beninese, and analyzed their relationships with pregnancy outcomes. Cytophilic IgG1 and IgG3 responses were the most frequent, with prevalences ranging from 28% (IgG3) up to 50% (IgG1). Elevated levels of VAR2CSA-specific total IgG and cytophilic IgG3 during pregnancy were consistently associated with higher birth weights, whilst high levels of IgG4 were associated with a reduced risk of placental infections. This suggests that protective anti-VAR2CSA IgG responses are coordinated between both cytophilic and non-cytophilic antibodies. Frontiers Media S.A. 2021-04-21 /pmc/articles/PMC8099026/ /pubmed/33968015 http://dx.doi.org/10.3389/fimmu.2021.610305 Text en Copyright © 2021 Tornyigah, d’Almeida, Escriou, Viwami, Fievet, Luty, Massougbodji, Nielsen, Deloron and Tuikue Ndam https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Tornyigah, Bernard
d’Almeida, Tania
Escriou, Guillaume
Viwami, Firmine
Fievet, Nadine
Luty, Adrian J. F.
Massougbodji, Achille
Nielsen, Morten A.
Deloron, Philippe
Tuikue Ndam, Nicaise
Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria
title Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria
title_full Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria
title_fullStr Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria
title_full_unstemmed Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria
title_short Plasmodium falciparum VAR2CSA-Specific IgG Subclass Responses Reflect Protection Against Low Birth Weight and Pregnancy-Associated Malaria
title_sort plasmodium falciparum var2csa-specific igg subclass responses reflect protection against low birth weight and pregnancy-associated malaria
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099026/
https://www.ncbi.nlm.nih.gov/pubmed/33968015
http://dx.doi.org/10.3389/fimmu.2021.610305
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