Recognition of Variant Rifin Antigens by Human Antibodies Induced during Natural Plasmodium falciparum Infections

MS Abdel-Latif, A Khattab, C Lindenthal… - Infection and …, 2002 - Am Soc Microbiol
MS Abdel-Latif, A Khattab, C Lindenthal, PG Kremsner, MQ Klinkert
Infection and immunity, 2002Am Soc Microbiol
Antibodies from individuals living in areas where malaria is endemic are known to react with
parasite-derived erythrocyte surface proteins. The major immunogenic and clonally variant
surface antigen described to date is Plasmodium falciparum erythrocyte membrane protein 1
(PfEMP-1), which is encoded by members of the multicopy var gene family. We report here
that rifin proteins (RIF proteins), belonging to the largest known family of variable infected
erythrocyte surface-expressed proteins, are also naturally immunogenic. Recombinant RIF …
Abstract
Antibodies from individuals living in areas where malaria is endemic are known to react with parasite-derived erythrocyte surface proteins. The major immunogenic and clonally variant surface antigen described to date is Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP-1), which is encoded by members of the multicopy var gene family. We report here that rifin proteins (RIF proteins), belonging to the largest known family of variable infected erythrocyte surface-expressed proteins, are also naturally immunogenic. Recombinant RIF proteins were used to analyze the antibody responses of individuals living in an area of intense malaria transmission. Elevated anti-rifin antibody levels were detected in the majority of the adult population tested, whereas the prevalence of such antibodies was much lower in malaria-exposed children. Despite the high degree of diversity between rif sequences and the high gene copy number, it appears that P. falciparum infections can induce antibodies that cross-react with several variant rifin molecules in many parasite isolates in a given community, and the immune response is most likely to be stable over time in a hyperendemic area. The protein was localized by fluorescence microscopy on the membrane of ring and young trophozoite-infected erythrocytes with antibodies from human immune sera with specificities for recombinant RIF protein.
American Society for Microbiology