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               <dc:title>Host age and expression of genes involved in red blood cell&#xd;
                invasion in Plasmodium falciparum field isolates</dc:title>
               <dc:creator>Valmaseda, Aida</dc:creator>
               <dc:creator>Bassat Orellana, Quique</dc:creator>
               <dc:creator>Aide, Pedro Carlos Paulino</dc:creator>
               <dc:creator>Cisteró, Pau</dc:creator>
               <dc:creator>Jiménez, Alfons</dc:creator>
               <dc:creator>Casellas, Aina</dc:creator>
               <dc:creator>Machevo, Sonia</dc:creator>
               <dc:creator>Aguilar, Ruth</dc:creator>
               <dc:creator>Sigaúque, Betuel</dc:creator>
               <dc:creator>Chauhan, Virander Singh</dc:creator>
               <dc:creator>Langer, Christine</dc:creator>
               <dc:creator>Beeson, James G.</dc:creator>
               <dc:creator>Chitnis, Chetan E.</dc:creator>
               <dc:creator>Alonso, Pedro</dc:creator>
               <dc:creator>Gaur, Deepak</dc:creator>
               <dc:creator>Mayor Aparicio, Alfredo Gabriel</dc:creator>
               <dc:subject>Plasmodium falciparum</dc:subject>
               <dc:subject>Hematies</dc:subject>
               <dc:subject>Plasmodium falciparum</dc:subject>
               <dc:subject>Erythrocytes</dc:subject>
               <dc:description>Plasmodium falciparum proteins involved in erythrocyte invasion&#xd;
                are main targets of acquired immunity and important vaccine&#xd;
                candidates. We hypothesized that anti-parasite immunity acquired&#xd;
                upon exposure would limit invasion-related gene (IRG) expression&#xd;
                and affect the clinical impact of the infection. 11 IRG&#xd;
                transcript levels were measured in P. falciparum isolates by&#xd;
                RT-PCR, and IgG/IgM against invasion ligands by Luminex(R), in&#xd;
                50 Mozambican adults, 25 children with severe malaria (SM) and&#xd;
                25 with uncomplicated malaria (UM). IRG expression differences&#xd;
                among groups and associations between IRG expression and&#xd;
                clinical/immunologic parameters were assessed. IRG expression&#xd;
                diversity was higher in parasites infecting children than adults&#xd;
                (p = 0.022). eba140 and ptramp expression decreased with age (p&#xd;
                = 0.003 and 0.007, respectively) whereas p41 expression&#xd;
                increased (p = 0.022). pfrh5 reduction in expression was abrupt&#xd;
                early in life. Parasite density decreased with increasing pfrh5&#xd;
                expression (p &lt; 0.001) and, only in children, parasite&#xd;
                density increased with p41 expression (p = 0.007), and decreased&#xd;
                with eba175 (p = 0.013). Antibody responses and IRG expression&#xd;
                were not associated. In conclusion, IRG expression is associated&#xd;
                with age and parasite density, but not with specific antibody&#xd;
                responses in the acute phase of infection. Our results confirm&#xd;
                the importance of multi-antigen vaccines development to avoid&#xd;
                parasite immune escape when tested in malaria-exposed&#xd;
                individuals.</dc:description>
               <dc:date>2017-07-21T12:08:19Z</dc:date>
               <dc:date>2017-07-21T12:08:19Z</dc:date>
               <dc:date>2017</dc:date>
               <dc:date>2017-07-19T18:00:12Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a:&#xd;
                http://dx.doi.org/10.1038/s41598-017-05025-5</dc:relation>
               <dc:relation>Scientific Reports, 2017, vol. 7, num. 1, p. 4717</dc:relation>
               <dc:relation>http://dx.doi.org/10.1038/s41598-017-05025-5</dc:relation>
               <dc:rights>cc by (c) Valmaseda, Aida et al., 2017</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Nature Publishing</dc:publisher>
               <dc:source>Articles publicats en revistes (ISGlobal)</dc:source>
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