%0 Journal Article
%9 ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES
%A Gnidehou, Sédami
%A Jessen, L.
%A Gangnard, S.
%A Ermont, Caroline
%A Triqui, Choukri
%A Quiviger, Mickaël
%A Guitard, Juliette
%A Lund, O.
%A Deloron, Philippe
%A Tuikue Ndam, Nicaise
%T Insight into antigenic diversity of VAR2CSA-DBL5 epsilon domain from multiple Plasmodium falciparum placental isolates
%D 2010
%L fdi:010052847
%G ENG
%J Plos One
%@ 1932-6203
%M ISI:000282359300011
%N 10
%P e13105
%R 10.1371/journal.pone.0013105
%U https://www.documentation.ird.fr/hor/fdi:010052847
%> https://horizon.documentation.ird.fr/exl-doc/pleins_textes/divers17-08/010052847.pdf
%V 5
%W Horizon (IRD)
%X Background: Protection against pregnancy associated malaria (PAM) is associated with high levels of anti-VAR2CSA antibodies. This protection is obtained by the parity dependent acquisition of anti-VAR2CSA antibodies. Distinct parity-associated molecular signatures have been identified in VAR2CSA domains. These two observations combined point to the importance of identifying VAR2CSA sequence variation, which facilitate parasitic evasion or subversion of host immune response. Highly conserved domains of VAR2CSA such as DBL5e are likely to contain conserved epitopes, and therefore do constitute attractive targets for vaccine development. Methodology/Principal Findings: VAR2CSA DBL5e-domain sequences obtained from cDNA of 40 placental isolates were analysed by a combination of experimental and in silico methods. Competition ELISA assays on two DBL5e variants, using plasma samples from women from two different areas and specific mice hyperimmune plasma, indicated that DBL5e possess conserved and cross-reactive B cell epitopes. Peptide ELISA identified conserved areas that are recognised by naturally acquired antibodies. Specific antibodies against these peptides labelled the native proteins on the surface of placental parasites. Despite high DBL5e sequence homology among parasite isolates, sequence analyses identified motifs in DBL5e that discriminate parasites according to donor's parity. Moreover, recombinant proteins of two VAR2CSA DBL5e variants displayed diverse recognition patterns by plasma from malaria-exposed women, and diverse proteoglycan binding abilities. Conclusions/Significance: This study provides insights into conserved and exposed B cell epitopes in DBL5e that might be a focus for cross reactivity. The importance of sequence variation in VAR2CSA as a critical challenge for vaccine development is highlighted. VAR2CSA conformation seems to be essential to its functionality. Therefore, identification of sequence variation sites in distinct locations within VAR2CSA, affecting antigenicity and/or binding properties, is critical to the effort of developing an efficient VAR2CSA-based vaccine. Motifs associated with parasite segregation according to parity constitute one such site.
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