Plasmodium vivax VIR Proteins are Targets of Naturally-Acquired Antibody and T cell Immune Responses to Malaria in Pregnant Women (Raw data)

P. vivax infection during pregnancy has been associated with poor outcomes such as anemia, low birth weight and congenital malaria, thus representing an important global health problem. However, no vaccine is currently available for its prevention. Vir genes were the first putative virulent factors...

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Detalles Bibliográficos
Autores: Adriana Malheiros, Alexandra J. Umbers, Alfredo Gabriel Mayor Aparicio, Azucena Bardají, Camila Botto Menezes, Carlo Severini, Carlota Dobaño, Carmen Fernández-Becerra, Chetan E. Chitnis, Clara Menéndez, Dhanpat K. Kochar, Dhiraj Hans, Edmilson Rui, Flor E. Martínez Espinosa, Francesca Mateo González, Hernando A. del Portillo Obando, Ivo Mueller, Maria Eugenia Castellanos, Maria Ome-Kaius, Meghna Desai, Michela Menegon, Myriam Arévalo Herrera, Norma Padilla, Pilar Requena, Regina A. Wangnapi, Sanjay K. Kochar, Sergi Sanz, Stephen John Rogerson, Swati Kochar
Tipo de recurso: conjunto de datos
Fecha de publicación:2022
País:España
Institución:Consorci de Serveis Universitaris de Catalunya (CSUC)
Repositorio:CORA.Repositori de Dades de Recerca
OAI Identifier:oai:dnet:cora.rdr____::e3c5f87e93ad2ec8c2e1ce35839e6563
Acceso en línea:https://doi.org/10.34810/DATA66
Access Level:acceso abierto
Palabra clave:Medicine, Health and Life Sciences
Plasmodium vivax
Immunoglobulins
Pregnant women
Malaria
Descripción
Sumario:P. vivax infection during pregnancy has been associated with poor outcomes such as anemia, low birth weight and congenital malaria, thus representing an important global health problem. However, no vaccine is currently available for its prevention. Vir genes were the first putative virulent factors associated with P. vivax infections, yet very few studies have examined their potential role as targets of immunity. We investigated the immunogenic properties of five VIR proteins and two long synthetic peptides containing conserved VIR sequences (PvLP1 and PvLP2) in the context of the PregVax cohort study including women from five malaria endemic countries: Brazil, Colombia, Guatemala, India and Papua New Guinea (PNG) at different timepoints during and after pregnancy. Antibody responses against all antigens were detected in all populations, with PNG women presenting the highest levels overall. P. vivax infection at sample collection time was positively associated with antibody levels against PvLP1 (fold-increase: 1.60 at recruitment -first antenatal visit-) and PvLP2 (fold-increase: 1.63 at delivery), and P. falciparum co-infection was found to increase those responses (for PvLP1 at recruitment, fold-increase: 2.25). Levels of IgG against two VIR proteins at delivery were associated with higher birth weight (27 g increase per duplicating antibody levels, p<0.5). Peripheral blood mononuclear cells from PNG uninfected pregnant women had significantly higher antigen-specific IFN-g TH1 responses (p=0.006) and secreted less pro-inflammatory cytokines TNF and IL-6 after PvLP2 stimulation than P. vivax-infected women (p<0.5). These data demonstrate that VIR antigens induce the natural acquisition of antibody and T cell memory responses that might be important in immunity to P. vivax during pregnancy in very diverse geographical settings.