<HashMap><database>biostudies-literature</database><scores/><additional><submitter>d'Almeida TC</submitter><funding>Agence Nationale de la Recherche</funding><pagination>9160</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6591392</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>Placental malaria has been associated with an immune tolerance phenomenon and a higher susceptibility to malaria infection during infancy. HLA-G is involved in fetal maternal immune tolerance by inhibiting maternal immunity. During infections HLA-G can be involved in immune escape of pathogens by creating a tolerogenic environment. Recent studies have shown an association between the risk of malaria and HLA-G at both genetic and protein levels. Moreover, women with placental malaria have a higher probability of giving birth to children exhibiting high sHLA-G, independently of their own level during pregnancy. Our aim was to explore the association between the level of maternal soluble HLA-G and the risk of malaria infection in their newborns. Here, 400 pregnant women and their children wer</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>High level of soluble human leukocyte antigen (HLA)-G at beginning of pregnancy as predictor of risk of malaria during infancy.</pubmed_title><pmcid>PMC6591392</pmcid><funding_grant_id>2010-PRSP-012 001</funding_grant_id><pubmed_authors>Sadissou I</pubmed_authors><pubmed_authors>Rouas-Freiss N</pubmed_authors><pubmed_authors>Milet J</pubmed_authors><pubmed_authors>Gineau L</pubmed_authors><pubmed_authors>Moreau P</pubmed_authors><pubmed_authors>Pennetier C</pubmed_authors><pubmed_authors>Carosella E</pubmed_authors><pubmed_authors>Cottrell G</pubmed_authors><pubmed_authors>Donadi EA</pubmed_authors><pubmed_authors>Moutairou K</pubmed_authors><pubmed_authors>Sabbagh A</pubmed_authors><pubmed_authors>Moiroux N</pubmed_authors><pubmed_authors>Courtin D</pubmed_authors><pubmed_authors>Sagbohan M</pubmed_authors><pubmed_authors>Garcia A</pubmed_authors><pubmed_authors>Avokpaho E</pubmed_authors><pubmed_authors>Favier B</pubmed_authors><pubmed_authors>Baldet T</pubmed_authors><pubmed_authors>d'Almeida TC</pubmed_authors></additional><is_claimable>false</is_claimable><name>High level of soluble human leukocyte antigen (HLA)-G at beginning of pregnancy as predictor of risk of malaria during infancy.</name><description>Placental malaria has been associated with an immune tolerance phenomenon and a higher susceptibility to malaria infection during infancy. HLA-G is involved in fetal maternal immune tolerance by inhibiting maternal immunity. During infections HLA-G can be involved in immune escape of pathogens by creating a tolerogenic environment. Recent studies have shown an association between the risk of malaria and HLA-G at both genetic and protein levels. Moreover, women with placental malaria have a higher probability of giving birth to children exhibiting high sHLA-G, independently of their own level during pregnancy. Our aim was to explore the association between the level of maternal soluble HLA-G and the risk of malaria infection in their newborns. Here, 400 pregnant women and their children wer</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2025-05-31T22:24:34.021Z</modification><creation>2025-05-31T22:24:34.021Z</creation></dates><accession>S-EPMC6591392</accession><cross_references><pubmed>31235762</pubmed><doi>10.1038/s41598-019-45688-w</doi></cross_references></HashMap>