Pathogenesis of Malaria

I.A Clark , L Schofield
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引用次数: 57

Abstract

As the mortality rate of 20–30% for severe falciparum malaria under even the best clinical conditions testifies, access to antimalarial drugs is not sufficient to prevent an appreciable mortality from this disease. Understanding the cause of death at a cellular level is essential if additional rational treatments are to be developed. Here, Ian Clark and Louis Schofield discuss recent work presented at the Molecular Approaches to Malaria conference, Lorne, Australia, 2–5 February 2000, that updates the cytokine-based concept of malarial disease.

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疟疾的发病机制
即使在最好的临床条件下,严重恶性疟疾的死亡率也高达20-30%,这证明,获得抗疟疾药物不足以防止这种疾病造成可观的死亡率。如果要开发更多合理的治疗方法,在细胞水平上了解死亡原因是必不可少的。本文中,Ian Clark和Louis Schofield讨论了2000年2月2日至5日在澳大利亚洛恩举行的疟疾分子方法会议上发表的最新研究成果,这些成果更新了基于细胞因子的疟疾概念。
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Websites of interest Neosporosis. Seeking new targets for antiparasitic agents Response from A. Serero et al. Parasitology nomenclature – a recommendation Implications for neonatal HIV/AIDS and TB of sensitization in utero to helminths
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