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东南亚卵形红细胞增多症带3预防巴布亚新几内亚儿童脑型疟疾。

Prevention of cerebral malaria in children in Papua New Guinea by southeast Asian ovalocytosis band 3.

作者信息

Allen S J, O'Donnell A, Alexander N D, Mgone C S, Peto T E, Clegg J B, Alpers M P, Weatherall D J

机构信息

Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, United Kingdom.

出版信息

Am J Trop Med Hyg. 1999 Jun;60(6):1056-60. doi: 10.4269/ajtmh.1999.60.1056.

Abstract

Southeast Asian ovalocytosis (SAO) occurs at high frequency in malarious regions of the western Pacific and may afford a survival advantage against malaria. It is caused by a deletion of the erythrocyte membrane band 3 gene and the band 3 protein mediates the cytoadherence of parasitized erythrocytes in vitro. The SAO band 3 variant may prevent cerebral malaria but it exacerbates malaria anemia and may also increase acidosis, a major determinant of mortality in malaria. We undertook a case-control study of children admitted to hospital in a malarious region of Papua New Guinea. The SAO band 3, detected by the polymerase chain reaction, was present in 0 of 68 children with cerebral malaria compared with six (8.8%) of 68 matched community controls (odds ratio = 0, 95% confidence interval = 0-0.85). Median hemoglobin levels were 1.2 g/dl lower in malaria cases with SAO than in controls (P = 0.035) but acidosis was not affected. The remarkable protection that SAO band 3 affords against cerebral malaria may offer a valuable approach to a better understanding of the mechanisms of adherence of parasitized erythrocytes to vascular endothelium, and thus of the pathogenesis of cerebral malaria.

摘要

东南亚卵形红细胞增多症(SAO)在西太平洋疟疾流行地区的发生率很高,可能对疟疾具有生存优势。它是由红细胞膜带3基因的缺失引起的,带3蛋白在体外介导被寄生红细胞的细胞黏附。SAO带3变体可能预防脑型疟疾,但会加重疟疾贫血,还可能增加酸中毒,而酸中毒是疟疾死亡率的一个主要决定因素。我们对巴布亚新几内亚疟疾流行地区住院的儿童进行了一项病例对照研究。通过聚合酶链反应检测到,68例脑型疟疾患儿中0例存在SAO带3,而68例匹配的社区对照中有6例(8.8%)存在(优势比=0,95%置信区间=0 - 0.85)。SAO疟疾病例的血红蛋白中位数水平比对照低1.2 g/dl(P = 0.035),但酸中毒未受影响。SAO带3对脑型疟疾的显著保护作用可能为更好地理解被寄生红细胞与血管内皮细胞黏附的机制以及脑型疟疾的发病机制提供有价值的途径。

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