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Tonkin, C.J., Carret, C.K., Duraisingh, M.T., Voss, T.S., Ralph, S.A., Hommel, M., Duffy, M.F., Silva, L.M., Scherf, A., Ivens, A., Speed, T.P., Beeson, J.G. and Cowman, A.F. (2009) Sir2 Paralogues Cooperate to Regulate Virulence Genes and Antigenic Variation in Plasmodium falciparum. PLoS Biology, 7, e1000084.
http://dx.doi.org/10.1371/journal.pbio.1000084

has been cited by the following article:

• TITLE: Immune evasion by Plasmodium falciparum parasites: converting a host protection mechanism for the parasite′s benefit

  AUTHORS: Bismarck Dinko, Gabriele Pradel

  KEYWORDS: Malaria, Plasmodium falciparum, Immune Evasion, Infected Red Blood Cell, Merozoite, Antibody, Complement, Factor H

  JOURNAL NAME: Advances in Infectious Diseases, Vol.6 No.2, June 28, 2016

  ABSTRACT: Immune evasion is a strategy used by pathogenic microbes to evade the host immune system in order to ensure successful propagation. Immune evasion is particularly important for the blood stages of Plasmodium falciparum, the causative agent of the deadly disease malaria tropica. Because Plasmodium blood stage parasites require human erythrocytes for replication, their ability to evade attack by the human immune system is essential for parasite survival. In order to escape immunity-induced killing, the intraerythrocytic parasites have evolved a variety of evasion mechanisms, including expansion of plasmodial surface proteins, organ-specific sequestration of the infected red blood cells and acquisition of immune-regulatory proteins by the parasite. This review aims to highlight recent advances in the molecular understanding of the immune evasion strategies by P. falciparum, including antigenic variation, surface protein polymorphisms and invasion ligand diversification. The review will further discuss new findings on the regulatory mechanisms applied by P. falciparum to avoid lysis by the human complement as well as killing by immune factors of the mosquito vector.