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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-17T12:17:50Z</responseDate> <request identifier=oai:HAL:hal-01668325v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-01668325v1</identifier> <datestamp>2017-12-21</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:sdv</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:UNIV-PARIS7</setSpec> <setSpec>collection:DSIMB</setSpec> <setSpec>collection:USPC</setSpec> <setSpec>collection:UNIV-REUNION</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Exacerbation of oxidative stress during sickle vaso-occlusive crisis is associated with decreased anti-band 3 autoantibodies rate and increased red blood cell-derived microparticle level: a prospective study</title> <creator>Hierso, Régine</creator> <creator>Lemonne, Nathalie</creator> <creator>Villaescusa, Rinaldo</creator> <creator>Lalanne-Mistrih, Marie-Laure</creator> <creator>Charlot, Keyne</creator> <creator>Etienne-Julan, Maryse</creator> <creator>Tressieres, Benoît</creator> <creator>Lamarre, Yann</creator> <creator>Tarer, Vanessa</creator> <creator>Garnier, Yohann</creator> <creator>Hernandez, Ada Arce</creator> <creator>Ferracci, Serge</creator> <creator>Connes, Philippe</creator> <creator>Romana, Marc</creator> <creator>Hardy-Dessources, Marie-Dominique</creator> <contributor>Biologie Intégrée du Globule Rouge ; Institut National de la Transfusion Sanguine [Paris] (INTS) - Université Paris Diderot - Paris 7 (UPD7) - Université de la Réunion (UR) - Institut National de la Santé et de la Recherche Médicale (INSERM) - CHU de Pointe-à-Pitre</contributor> <contributor>Unité Transversale de la Drépanocytose ; CHU Pointe-à-Pitre/Abymes</contributor> <contributor>Institut d'hématologie et d'immunologie, La Havane</contributor> <contributor>Centre d'investigation clinique Antilles-Guyane ; Institut National de la Santé et de la Recherche Médicale (INSERM) - CH Cayenne</contributor> <contributor>Biologie intégrée du globule rouge ; Université des Antilles et de la Guyane (UAG) - Institut National de la Transfusion Sanguine [Paris] (INTS) - Université Paris Diderot - Paris 7 (UPD7) - Institut National de la Santé et de la Recherche Médicale (INSERM)</contributor> <contributor>Centre d'Investigation Clinique Antilles-Guyane (CIC - Antilles Guyane) ; Université des Antilles et de la Guyane (UAG) - Institut National de la Santé et de la Recherche Médicale (INSERM) - CHU de Pointe-à-Pitre - Centre Hospitalier de Cayenne Andrée Rosemon - CHU de Fort de France</contributor> <contributor>Dynamique des Structures et Interactions des Macromolécules Biologiques- Pôle de La Réunion (DSIMB Réunion) ; Dynamique des Structures et Interactions des Macromolécules Biologiques (DSIMB) ; Institut National de la Transfusion Sanguine [Paris] (INTS) - Université Paris Diderot - Paris 7 (UPD7) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Institut National de la Transfusion Sanguine [Paris] (INTS) - Université Paris Diderot - Paris 7 (UPD7) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Université de la Réunion (UR)</contributor> <contributor>Service d'Orthopédie et de Traumatologie ; Université des Antilles et de la Guyane (UAG) - CHU Pointe-à-Pitre/Abymes</contributor> <contributor>Centre Hospitalo-Universitaire de Pointe-à-Pitre/Abymes</contributor> <contributor>Protéines de la membrane érythrocytaire et homologues non-érythroides ; Université des Antilles et de la Guyane (UAG) - Institut National de la Transfusion Sanguine [Paris] (INTS) - Université Paris Diderot - Paris 7 (UPD7) - Université de la Réunion (UR) - Institut National de la Santé et de la Recherche Médicale (INSERM)</contributor> <description>International audience</description> <source>ISSN: 0007-1048</source> <source>EISSN: 1365-2141</source> <source>British Journal of Haematology</source> <publisher>Wiley</publisher> <identifier>hal-01668325</identifier> <identifier>https://hal.univ-antilles.fr/hal-01668325</identifier> <source>https://hal.univ-antilles.fr/hal-01668325</source> <source>British Journal of Haematology, Wiley, 2017, 176 (5), pp.805 - 813. 〈10.1111/bjh.14476〉</source> <identifier>DOI : 10.1111/bjh.14476</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1111/bjh.14476</relation> <language>en</language> <subject lang=en>microparticles</subject> <subject lang=en> natural anti-band 3 antibodies</subject> <subject lang=en> oxidative stress</subject> <subject lang=en> painful vaso-occlusive crisis</subject> <subject lang=en> sickle cell anaemia</subject> <subject>[SDV.MHEP.HEM] Life Sciences [q-bio]/Human health and pathology/Hematology</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>Painful vaso-occlusive crisis, a hallmark of sickle cell anaemia, results from complex, incompletely understood mechanisms. Red blood cell (RBC) damage caused by continuous endogenous and exogenous oxidative stress may precipitate the occurrence of vaso-occlusive crises. In order to gain insight into the relevance of oxidative stress in vaso-occlusive crisis occurrence, we prospectively compared the expression levels of various oxidative markers in 32 adults with sickle cell anaemia during vaso-occlusive crisis and steady-state conditions. Compared to steady-state condition, plasma levels of free haem, advanced oxidation protein products and myeloperoxidase, RBC caspase-3 activity, as well as the concentrations of total, neutrophil- and RBC-derived microparticles were increased during vaso-occlusive crises, whereas the reduced glutathione content was decreased in RBCs. In addition, natural anti-band 3 autoantibodies levels decreased during crisis and were negatively correlated with the rise in plasma advanced oxidation protein products and RBC caspase-3 activity. These data showed an exacerbation of the oxidative stress during vaso-occlusive crises in sickle cell anaemia patients and strongly suggest that the higher concentration of harmful circulating RBC-derived microparticles and the reduced anti-band 3 autoantibodies levels may be both related to the recruitment of oxidized band 3 into membrane aggregates.</description> <date>2017-03</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>