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https://doi.org/10.3389/fimmu.2016.00463
Title: | Malaria parasites: The great escape | Authors: | Rénia, L Goh, Y.S |
Keywords: | epitope gamma interferon glycosylphosphatidylinositol heat shock protein 70 immunoglobulin G1 immunoglobulin G3 immunoglobulin M intercellular adhesion molecule 1 vaccine antigenic variation B lymphocyte CD4+ T lymphocyte cell adhesion cell invasion complement system cross reaction histology immune deficiency immune evasion Kupffer cell malaria falciparum nonhuman parasite survival phagocytosis Plasmodium protein polymorphism Review |
Issue Date: | 2016 | Citation: | Rénia, L, Goh, Y.S (2016). Malaria parasites: The great escape. Frontiers in Immunology 7 (NOV) : 463. ScholarBank@NUS Repository. https://doi.org/10.3389/fimmu.2016.00463 | Rights: | Attribution 4.0 International | Abstract: | Parasites of the genus Plasmodium have a complex life cycle. They alternate between their final mosquito host and their intermediate hosts. The parasite can be either extra- or intracellular, depending on the stage of development. By modifying their shape, motility, and metabolic requirements, the parasite adapts to the different environments in their different hosts. The parasite has evolved to escape the multiple immune mechanisms in the host that try to block parasite development at the different stages of their development. In this article, we describe the mechanisms reported thus far that allow the Plasmodium parasite to evade innate and adaptive immune responses. © 2016 Rénia and Goh. | Source Title: | Frontiers in Immunology | URI: | https://scholarbank.nus.edu.sg/handle/10635/179902 | ISSN: | 16643224 | DOI: | 10.3389/fimmu.2016.00463 | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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