Antimalarial drugs reduce cytoadherence and resetting of Plasmodium falciparum

被引:71
作者
Udomsangpetch, R
Pipitaporn, B
Krishna, S
Angus, B
Pukrittayakamee, S
Bates, I
Suputtamongkol, Y
Kyle, DE
White, NJ
机构
[1] MAHIDOL UNIV,FAC TROP MED,BANGKOK 10400,THAILAND
[2] MAHIDOL UNIV,FAC SCI,DEPT PATHOBIOL,BANGKOK 10400,THAILAND
[3] USAF,DEPT IMMUNOL,INST MED SCI,BANGKOK,THAILAND
[4] JOHN RADCLIFFE HOSP,NUFFIELD DEPT CLIN MED,OXFORD OX3 9DU,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1093/infdis/173.3.691
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The in vivo and in vitro effects of antimalarials on cytoadherence and rosette formation were studied in 17 patients with severe and 46 with uncomplicated falciparum malaria. Cytoadherence was increased in severe malaria (P < .001). Artesunate and artemether were more potent than quinine in inhibiting both adherence properties. Artesunate was the most rapidly acting drug tested, producing > 50% inhibition of both cytoadherence and resetting in vivo and in vitro within 2 h of drug exposure. Exposure to quinine for greater than or equal to 4 h in vivo reduced resetting by > 50%, but not cytoadherence. Quinine did not reduce cytoadherence or resetting significantly in vitro with exposure times of less than or equal to 8 h. These results suggest that artemisinin derivatives are more effective than quinine in preventing pathologic processes in parasitized erythrocytes that contribute to microvascular obstruction in severe malaria.
引用
收藏
页码:691 / 698
页数:8
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