Plasmodium falciparumAntigenic Variation: Relationships between In Vivo Selection, Acquired Antibody Response, and Disease Severity
Author(s) -
Peter C. Bull,
Arnab Pain,
Francis M. Ndungu,
Samson Kinyanjui,
David J. Roberts,
Chris Newbold,
Kevin Marsh
Publication year - 2005
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/432761
Subject(s) - malaria , antibody , biology , immunology , antigen , plasmodium falciparum , antigenic variation , immune system , virology
Variant surface antigens (VSA) on Plasmodium falciparum-infected erythrocytes are potentially important targets of immunity to malaria. We previously identified a VSA phenotype--VSA with a high frequency of antibody recognition (VSA(FoRH))--that is associated with young host age and severe malaria. We hypothesized that VSA(FoRH) are positively selected by host molecules such as intercellular adhesion molecule 1 (ICAM1) and CD36 and dominate in the absence of an effective immune response. Here, we assessed, in 115 Kenyan children, the potential role played by in vivo selection pressures in either favoring or selecting against VSA(FoRH) among parasites that cause malaria.
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