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<jats:p><jats:named-content content-type="genus-species">Plasmodium falciparum</jats:named-content>erythrocyte membrane protein 1 (PfEMP1), expressed on<jats:named-content content-type="genus-species">P. falciparum-</jats:named-content>infected erythrocytes, is a major family of clonally variant targets of naturally acquired immunity to malaria. Previous studies have demonstrated that in areas where malaria is endemic, antibodies to infected erythrocytes from children with severe malaria tend to be more seroprevalent than antibodies to infected erythrocytes from children with nonsevere malaria. These data have led to a working hypothesis that PfEMP1 variants associated with parasite virulence are relatively conserved in structure. However, the longevity of such serologically conserved variants in the parasite population is unknown. Here, using infected erythrocytes from recently sampled clinical<jats:named-content content-type="genus-species">P. falciparum</jats:named-content>samples, we measured serological conservation using pools of antibodies in sera that had been sampled 10 to 12 years earlier. The serological conservation of infected erythrocytes strongly correlated with the expression of specific PfEMP1 subsets previously found to be associated with severe malaria. However, we found no association between serological conservation<jats:italic>per se</jats:italic>and disease severity within these data. This contrasts with the simple hypothesis that<jats:named-content content-type="genus-species">P. falciparum</jats:named-content>isolates with a serologically conserved group of PfEMP1 variants cause severe malaria. The data are instead consistent with periodic turnover of the immunodominant epitopes of PfEMP1 associated with severe malaria.</jats:p>

Original publication

DOI

10.1128/iai.00772-15

Type

Journal article

Journal

Infection and Immunity

Publisher

American Society for Microbiology

Publication Date

05/2016

Volume

84

Pages

1331 - 1335