Publications des scientifiques de l'IRD

Badaut C., Visitdesotrakul P., Chabry A., Bigey P., Tornyigah B., Roman Jocelyne, Maroufou J. A., Amoussou A., Ayivi B. S., Sagbo G., Tuikue Ndam Nicaise, Oleinikov A. V., Tahar Rachida. (2021). IgG acquisition against PfEMP1 PF11_0521 domain cassette DC13, DBL beta 3_D4 domain, and peptides located within these constructs in children with cerebral malaria. Scientific Reports - Nature, 11 (1), p. 3680 [12 p.]. ISSN 2045-2322.

Titre du document
IgG acquisition against PfEMP1 PF11_0521 domain cassette DC13, DBL beta 3_D4 domain, and peptides located within these constructs in children with cerebral malaria
Année de publication
2021
Type de document
Article référencé dans le Web of Science WOS:000626726100053
Auteurs
Badaut C., Visitdesotrakul P., Chabry A., Bigey P., Tornyigah B., Roman Jocelyne, Maroufou J. A., Amoussou A., Ayivi B. S., Sagbo G., Tuikue Ndam Nicaise, Oleinikov A. V., Tahar Rachida
Source
Scientific Reports - Nature, 2021, 11 (1), p. 3680 [12 p.] ISSN 2045-2322
The Plasmodium falciparum erythrocyte-membrane-protein-1 (PF3D7_1150400/PF11_0521) contains both domain cassette DC13 and DBL beta 3 domain binding to EPCR and ICAM-1 receptors, respectively. This type of PfEMP1 proteins with dual binding specificity mediate specific interactions with brain micro-vessels endothelium leading to the development of cerebral malaria (CM). Using plasma collected from children at time of hospital admission and after 30 days, we study an acquisition of IgG response to PF3D7_1150400/PF11_0521 DC13 and DBL beta 3_D4 recombinant constructs, and five peptides located within these constructs, specifically in DBL alpha 1.7_D2 and DBL beta 3_D4 domains. We found significant IgG responses against the entire DC13, PF11_0521_DBL beta 3_D4 domain, and peptides. The responses varied against different peptides and depended on the clinical status of children. The response was stronger at day 30, and mostly did not differ between CM and uncomplicated malaria (UM) groups. Specifically, the DBL beta 3 B3-34 peptide that contains essential residues involved in the interaction between PF11_0521 DBL beta 3_D4 domain and ICAM-1 receptor demonstrated significant increase in reactivity to IgG1 and IgG3 antibodies at convalescence. Further, IgG reactivity in CM group at time of admission against functionally active (ICAM-1-binding) PF11_0521 DBL beta 3_D4 domain was associated with protection against severe anemia. These results support development of vaccine based on the PF3D7_1150400/PF11_0521 structures to prevent CM.
Plan de classement
Sciences fondamentales / Techniques d'analyse et de recherche [020] ; Santé : généralités [050] ; Entomologie médicale / Parasitologie / Virologie [052]
Localisation
Fonds IRD [F B010081257]
Identifiant IRD
fdi:010081257
Contact