Red blood cell defects and malaria

被引:59
|
作者
Williams, Thomas N.
机构
[1] Kemri Wellcome Trust Collaborat Programme, Kilifi, Kenya
[2] Churchill Hosp, Nuffield Dept Med, Ctr Clin Vaccinol & Trop Med, Oxford OX3 7LJ, England
基金
英国惠康基金;
关键词
malaria; human genetics; red blood cell;
D O I
10.1016/j.molbiopara.2006.05.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malaria is a major cause of childhood death throughout much of the tropical world. As a result, it has exerted a powerful force for the evolutionary selection of genes that confer a survival advantage. Identifying which genes are involved, and how they affect malaria risk, is a potentially useful way of exploring the host-parasite relationship. To date, some of the best-described malaria-protective polymorphisms relate to genes that affect the structure or function of red blood cells (RBC). Recent years have seen significant advances in our understanding of the importance of some of these genes, including glycophorin C (GYPC); complement receptor 1 (CR1); band 3 (SLC4A1); pyruvate kinase (Pklr); and the genes for alpha-(HBA) and beta-globin (HBB). The challenge for the future must be to convert these advances into fresh approaches to the prevention and treatment of malaria. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:121 / 127
页数:7
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