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Antigenic variation at the infected red cell surface in malaria
S Kyes1, P Horrocks, C Newbold
1Molecular Parasitology Group, Weatherall Institute of Molecular Medicine, Headington, Oxford OX3 9DS United Kingdom. skyes@molbiol.ox.ac.uk
Annual Review of Microbiology
|September 7, 2001
Summary
Pathogens like malaria parasites evade immune systems using clonal antigenic variation. This involves switching surface molecules to avoid detection, ensuring long-term infection and survival in hosts.
Area of Science:
- Parasitology
- Immunology
- Molecular Biology
Background:
- Many pathogens have evolved immune evasion strategies to ensure long-term host survival.
- Clonal antigenic variation is a common immune evasion mechanism used by pathogens like Plasmodium, Trypanosoma, and Borrelia.
Purpose of the Study:
- To review the history and recent data on antigenic variation in malaria parasites.
- To focus on Plasmodium falciparum, the causative agent of severe human malaria.
Main Methods:
- Review of historical and current scientific literature on antigenic variation.
- Analysis of gene families encoding surface molecules involved in immune evasion.
- Emphasis on Plasmodium falciparum as a model system.
Main Results:
- Antigenic variation relies on the sequential expression of diverse surface molecules from multicopy, nonallelic gene families.
- These molecules are targets of the host's humoral immune response.
- In Plasmodium, some variant surface molecules are also critical virulence factors.
Conclusions:
- Antigenic variation is a key survival strategy for Plasmodium falciparum, complicating host-parasite interactions.
- Understanding this mechanism is crucial for developing effective malaria control strategies.
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