IgG antibodies to synthetic GPI are biomarkers of immune-status to both Plasmodium falciparum and Plasmodium vivax malaria in young children
Identifieur interne : 000A32 ( Main/Exploration ); précédent : 000A31; suivant : 000A33IgG antibodies to synthetic GPI are biomarkers of immune-status to both Plasmodium falciparum and Plasmodium vivax malaria in young children
Auteurs : Camila T. França ; Connie S. N. Li Wai Suen ; Amandine Carmagnac ; Enmoore Lin ; Benson Kiniboro ; Peter Siba ; Louis Schofield ; Ivo Mueller [France, Espagne]Source :
- Malaria Journal [ 1475-2875 ] ; 2017.
Abstract
Further reduction in malaria prevalence and its eventual elimination would be greatly facilitated by the development of biomarkers of exposure and/or acquired immunity to malaria, as well as the deployment of effective vaccines against
ELISA was used to measure total IgG to a synthetic form of glycosylphosphatidylinositol from
Total IgG levels to
This study highlights that in young children, IgG to
The online version of this article (doi:10.1186/s12936-017-2042-2) contains supplementary material, which is available to authorized users.
Url:
DOI: 10.1186/s12936-017-2042-2
PubMed: 28946883
PubMed Central: 5613389
Affiliations:
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malaria in young children</title>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">IgG antibodies to synthetic GPI are biomarkers of immune-status to both <italic>Plasmodium falciparum</italic>
and <italic>Plasmodium vivax</italic>
malaria in young children</title>
<author><name sortKey="Franca, Camila T" sort="Franca, Camila T" uniqKey="Franca C" first="Camila T." last="França">Camila T. França</name>
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<author><name sortKey="Li Wai Suen, Connie S N" sort="Li Wai Suen, Connie S N" uniqKey="Li Wai Suen C" first="Connie S. N." last="Li Wai Suen">Connie S. N. Li Wai Suen</name>
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<author><name sortKey="Carmagnac, Amandine" sort="Carmagnac, Amandine" uniqKey="Carmagnac A" first="Amandine" last="Carmagnac">Amandine Carmagnac</name>
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</affiliation>
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<author><name sortKey="Lin, Enmoore" sort="Lin, Enmoore" uniqKey="Lin E" first="Enmoore" last="Lin">Enmoore Lin</name>
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<wicri:noCountry code="subfield">Madang Province Papua New Guinea</wicri:noCountry>
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<author><name sortKey="Kiniboro, Benson" sort="Kiniboro, Benson" uniqKey="Kiniboro B" first="Benson" last="Kiniboro">Benson Kiniboro</name>
<affiliation><nlm:aff id="Aff4">Malaria Immuno-Epidemiology Unit, PNG Institute of Medical Research, Madang, Madang Province Papua New Guinea</nlm:aff>
<wicri:noCountry code="subfield">Madang Province Papua New Guinea</wicri:noCountry>
</affiliation>
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<author><name sortKey="Siba, Peter" sort="Siba, Peter" uniqKey="Siba P" first="Peter" last="Siba">Peter Siba</name>
<affiliation><nlm:aff id="Aff4">Malaria Immuno-Epidemiology Unit, PNG Institute of Medical Research, Madang, Madang Province Papua New Guinea</nlm:aff>
<wicri:noCountry code="subfield">Madang Province Papua New Guinea</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Schofield, Louis" sort="Schofield, Louis" uniqKey="Schofield L" first="Louis" last="Schofield">Louis Schofield</name>
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Parkville, VIC Australia</nlm:aff>
<wicri:noCountry code="subfield">VIC Australia</wicri:noCountry>
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Townsville, QLD Australia</nlm:aff>
<wicri:noCountry code="subfield">QLD Australia</wicri:noCountry>
</affiliation>
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<author><name sortKey="Mueller, Ivo" sort="Mueller, Ivo" uniqKey="Mueller I" first="Ivo" last="Mueller">Ivo Mueller</name>
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<institution>Barcelona Institute of Global Health (ISGLOBAL),</institution>
</institution-wrap>
Barcelona, Spain</nlm:aff>
<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Barcelona</wicri:regionArea>
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<series><title level="j">Malaria Journal</title>
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<imprint><date when="2017">2017</date>
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p id="Par1">Further reduction in malaria prevalence and its eventual elimination would be greatly facilitated by the development of biomarkers of exposure and/or acquired immunity to malaria, as well as the deployment of effective vaccines against <italic>Plasmodium falciparum</italic>
and <italic>Plasmodium vivax.</italic>
A better understanding of the acquisition of immunity in naturally-exposed populations is essential for the identification of antigens useful as biomarkers, as well as to inform rational vaccine development.</p>
</sec>
<sec><title>Methods</title>
<p id="Par2">ELISA was used to measure total IgG to a synthetic form of glycosylphosphatidylinositol from <italic>P. falciparum</italic>
(<italic>Pf</italic>
GPI) in a cohort of 1–3 years old Papua New Guinea children with well-characterized individual differences in exposure to <italic>P. falciparum</italic>
and <italic>P. vivax</italic>
blood-stage infections. The relationship between IgG levels to <italic>Pf</italic>
GPI and measures of recent and past exposure to <italic>P. falciparum</italic>
and <italic>P. vivax</italic>
infections was investigated, as well as the association between antibody levels and prospective risk of clinical malaria over 16 months of follow-up.</p>
</sec>
<sec><title>Results</title>
<p id="Par3">Total IgG levels to <italic>Pf</italic>
GPI were low in the young children tested. Antibody levels were higher in the presence of <italic>P. falciparum</italic>
or <italic>P. vivax</italic>
infections, but short-lived. High IgG levels were associated with higher risk of <italic>P. falciparum</italic>
malaria (IRR 1.33–1.66, P = 0.008–0.027), suggesting that they are biomarkers of increased exposure to <italic>P. falciparum</italic>
infections. Given the cross-reactive nature of antibodies to <italic>Pf</italic>
GPI, high IgG levels were also associated with reduced risk of <italic>P. vivax</italic>
malaria (IRR 0.65–0.67, P = 0.039–0.044), indicating that these antibodies are also markers of acquired immunity to <italic>P. vivax</italic>
.</p>
</sec>
<sec><title>Conclusions</title>
<p id="Par4">This study highlights that in young children, IgG to <italic>Pf</italic>
GPI might be a useful marker of immune-status to both <italic>P. falciparum</italic>
and <italic>P. vivax</italic>
infections, and potentially useful to help malaria control programs to identify populations at-risk. Further functional studies are necessary to confirm the potential of <italic>Pf</italic>
GPI as a target for vaccine development.</p>
</sec>
<sec><title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/s12936-017-2042-2) contains supplementary material, which is available to authorized users.</p>
</sec>
</div>
</front>
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<author><name sortKey="Diatta, B" uniqKey="Diatta B">B Diatta</name>
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<author><name sortKey="Niang, B" uniqKey="Niang B">B Niang</name>
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<author><name sortKey="Diagne, N" uniqKey="Diagne N">N Diagne</name>
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<author><name sortKey="Ndiaye, M" uniqKey="Ndiaye M">M Ndiaye</name>
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<author><name sortKey="Marrama, L" uniqKey="Marrama L">L Marrama</name>
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<author><name sortKey="Fagan, Pk" uniqKey="Fagan P">PK Fagan</name>
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<author><name sortKey="Lagog, M" uniqKey="Lagog M">M Lagog</name>
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<author><name sortKey="Mgone, Cs" uniqKey="Mgone C">CS Mgone</name>
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<name sortKey="Franca, Camila T" sort="Franca, Camila T" uniqKey="Franca C" first="Camila T." last="França">Camila T. França</name>
<name sortKey="Kiniboro, Benson" sort="Kiniboro, Benson" uniqKey="Kiniboro B" first="Benson" last="Kiniboro">Benson Kiniboro</name>
<name sortKey="Li Wai Suen, Connie S N" sort="Li Wai Suen, Connie S N" uniqKey="Li Wai Suen C" first="Connie S. N." last="Li Wai Suen">Connie S. N. Li Wai Suen</name>
<name sortKey="Lin, Enmoore" sort="Lin, Enmoore" uniqKey="Lin E" first="Enmoore" last="Lin">Enmoore Lin</name>
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