Dynamics of PfEMP1 Antibody Profile from Birth to 12 Months of Age in Beninese Infants

A. Moussiliou, L. Turner, L. Turner, G. Cottrell, J. Doritchamou, K. Gbédandé, N. Fievet, A. J.F. Luty, A. Massougbodji, T. G. Theander, T. G. Theander, P. Deloron, T. Lavstsen, T. Lavstsen, N. Tuikue Ndam

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Background: Plasmodium falciparum-infected erythrocytes bind to specific endothelial cell receptors via members of the PfEMP1 family exported onto the erythrocyte surface. These interactions are mediated by different types of cysteine-rich interdomain region (CIDR) domains found in the N-terminal region of all PfEMP1. CIDRα1 domains bind endothelial protein C receptor (EPCR), CIDRα2-6 domains bind CD36, whereas the receptor specificity of CIDRβ/γ/δdomains is unknown. Methods: In this study, we investigated the level of immunoglobulin (Ig)G targeting the different types of PfEMP1 CIDR during the first year of life. We used plasma collected longitudinally from children of pregnant women who had been followed closely through pregnancy. Results: Antibodies to CIDRα1 domains were more frequent in cord blood compared with antibodies to CIDRα2-6 domains. Higher IgG levels to EPCR-binding CIDRα1 variants positively correlated with the timing of first infections. Antibodies to all PfEMP1 types declined at similar rates to the point of disappearance over the first 6 months of life. At 12 months, children had acquired antibody to all types of CIDR domains, mostly in children with documented P falciparum infections. Conclusions: These observations agree with the notion that the timing and phenotype of first P falciparum infections in life are influenced by the immune status of the mother.

Original languageEnglish (US)
Pages (from-to)2010-2017
Number of pages8
JournalJournal of Infectious Diseases
Volume221
Issue number12
DOIs
StatePublished - Jun 11 2020
Externally publishedYes

Keywords

  • CIDR domains
  • IgG
  • PfEMP1
  • children
  • malaria

ASJC Scopus subject areas

  • General Medicine

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