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Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP)

BACKGROUND: Children below six months are reported to be less susceptible to clinical malaria. Maternally derived antibodies and foetal haemoglobin are important putative protective factors. We examined antibodies to Plasmodium falciparum merozoite surface protein 3 (MSP3) and glutamate-rich protein...

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Autores principales: Kangoye, David Tiga, Nebie, Issa, Yaro, Jean-Baptiste, Debe, Siaka, Traore, Safiatou, Ouedraogo, Oumarou, Sanou, Guillaume, Soulama, Issiaka, Diarra, Amidou, Tiono, Alfred, Marsh, Kevin, Sirima, Sodiomon Bienvenu, Bejon, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169582/
https://www.ncbi.nlm.nih.gov/pubmed/25238160
http://dx.doi.org/10.1371/journal.pone.0107965
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author Kangoye, David Tiga
Nebie, Issa
Yaro, Jean-Baptiste
Debe, Siaka
Traore, Safiatou
Ouedraogo, Oumarou
Sanou, Guillaume
Soulama, Issiaka
Diarra, Amidou
Tiono, Alfred
Marsh, Kevin
Sirima, Sodiomon Bienvenu
Bejon, Philip
author_facet Kangoye, David Tiga
Nebie, Issa
Yaro, Jean-Baptiste
Debe, Siaka
Traore, Safiatou
Ouedraogo, Oumarou
Sanou, Guillaume
Soulama, Issiaka
Diarra, Amidou
Tiono, Alfred
Marsh, Kevin
Sirima, Sodiomon Bienvenu
Bejon, Philip
author_sort Kangoye, David Tiga
collection PubMed
description BACKGROUND: Children below six months are reported to be less susceptible to clinical malaria. Maternally derived antibodies and foetal haemoglobin are important putative protective factors. We examined antibodies to Plasmodium falciparum merozoite surface protein 3 (MSP3) and glutamate-rich protein (GLURP), in children in their first two years of life in Burkina Faso and their risk of malaria. METHODS: A cohort of 140 infants aged between four and six weeks was recruited in a stable transmission area of south-western Burkina Faso and monitored for 24 months by active and passive surveillance. Malaria infections were detected by examining blood smears using light microscopy. Enzyme-linked immunosorbent assay was used to quantify total Immunoglobulin G to Plasmodium falciparum antigens MSP3 and two regions of GLURP (R0 and R2) on blood samples collected at baseline, three, six, nine, 12, 18 and 24 months. Foetal haemoglobin and variant haemoglobin fractions were measured at the baseline visit using high pressure liquid chromatography. RESULTS: A total of 79.6% of children experienced one or more episodes of febrile malaria during monitoring. Antibody titres to MSP3 were prospectively associated with an increased risk of malaria while antibody responses to GLURP (R0 and R2) did not alter the risk. Antibody titres to MSP3 were higher among children in areas of high malaria risk. Foetal haemoglobin was associated with delayed first episode of febrile malaria and haemoglobin CC type was associated with reduced incidence of febrile malaria. CONCLUSIONS: We did not find any evidence of association between titres of antibodies to MSP3, GLURP-R0 or GLURP-R2 as measured by enzyme-linked immunosorbent assay and early protection against malaria, although anti-MSP3 antibody titres may reflect increased exposure to malaria and therefore greater risk. Foetal haemoglobin was associated with protection against febrile malaria despite the study limitations and its role is therefore worthy further investigation.
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spelling pubmed-41695822014-09-22 Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP) Kangoye, David Tiga Nebie, Issa Yaro, Jean-Baptiste Debe, Siaka Traore, Safiatou Ouedraogo, Oumarou Sanou, Guillaume Soulama, Issiaka Diarra, Amidou Tiono, Alfred Marsh, Kevin Sirima, Sodiomon Bienvenu Bejon, Philip PLoS One Research Article BACKGROUND: Children below six months are reported to be less susceptible to clinical malaria. Maternally derived antibodies and foetal haemoglobin are important putative protective factors. We examined antibodies to Plasmodium falciparum merozoite surface protein 3 (MSP3) and glutamate-rich protein (GLURP), in children in their first two years of life in Burkina Faso and their risk of malaria. METHODS: A cohort of 140 infants aged between four and six weeks was recruited in a stable transmission area of south-western Burkina Faso and monitored for 24 months by active and passive surveillance. Malaria infections were detected by examining blood smears using light microscopy. Enzyme-linked immunosorbent assay was used to quantify total Immunoglobulin G to Plasmodium falciparum antigens MSP3 and two regions of GLURP (R0 and R2) on blood samples collected at baseline, three, six, nine, 12, 18 and 24 months. Foetal haemoglobin and variant haemoglobin fractions were measured at the baseline visit using high pressure liquid chromatography. RESULTS: A total of 79.6% of children experienced one or more episodes of febrile malaria during monitoring. Antibody titres to MSP3 were prospectively associated with an increased risk of malaria while antibody responses to GLURP (R0 and R2) did not alter the risk. Antibody titres to MSP3 were higher among children in areas of high malaria risk. Foetal haemoglobin was associated with delayed first episode of febrile malaria and haemoglobin CC type was associated with reduced incidence of febrile malaria. CONCLUSIONS: We did not find any evidence of association between titres of antibodies to MSP3, GLURP-R0 or GLURP-R2 as measured by enzyme-linked immunosorbent assay and early protection against malaria, although anti-MSP3 antibody titres may reflect increased exposure to malaria and therefore greater risk. Foetal haemoglobin was associated with protection against febrile malaria despite the study limitations and its role is therefore worthy further investigation. Public Library of Science 2014-09-19 /pmc/articles/PMC4169582/ /pubmed/25238160 http://dx.doi.org/10.1371/journal.pone.0107965 Text en © 2014 Kangoye et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kangoye, David Tiga
Nebie, Issa
Yaro, Jean-Baptiste
Debe, Siaka
Traore, Safiatou
Ouedraogo, Oumarou
Sanou, Guillaume
Soulama, Issiaka
Diarra, Amidou
Tiono, Alfred
Marsh, Kevin
Sirima, Sodiomon Bienvenu
Bejon, Philip
Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP)
title Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP)
title_full Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP)
title_fullStr Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP)
title_full_unstemmed Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP)
title_short Plasmodium falciparum Malaria in Children Aged 0-2 Years: The Role of Foetal Haemoglobin and Maternal Antibodies to Two Asexual Malaria Vaccine Candidates (MSP3 and GLURP)
title_sort plasmodium falciparum malaria in children aged 0-2 years: the role of foetal haemoglobin and maternal antibodies to two asexual malaria vaccine candidates (msp3 and glurp)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169582/
https://www.ncbi.nlm.nih.gov/pubmed/25238160
http://dx.doi.org/10.1371/journal.pone.0107965
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