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Continuation of chloroquine-susceptible Plasmodium falciparum parasitemia in volunteers receiving chloroquine therapy.接受氯喹治疗的志愿者中氯喹敏感型恶性疟原虫血症的持续情况。
Antimicrob Agents Chemother. 1990 Apr;34(4):676-9. doi: 10.1128/AAC.34.4.676.
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Early activity in sporozoite-induced Plasmodium falciparum infections.疟原虫诱导的恶性疟原虫感染中的早期活动。
Ann Trop Med Parasitol. 1959 Apr;53(1):51-8. doi: 10.1080/00034983.1959.11685899.
2
Studies on the chemotherapy of malaria. VII. The treatment of acute malaria in Malaya.疟疾化疗研究。VII. 马来亚急性疟疾的治疗。
Med J Malaya. 1958 Mar;12(3):471-99.
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Cloning of naturally occurring mixed infections of malaria parasites.疟原虫自然发生的混合感染的克隆
Science. 1981 May 29;212(4498):1037-8. doi: 10.1126/science.7015505.
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Host defenses in murine malaria: analysis of plasmodial infection-caused defects in macrophage microbicidal capacities.小鼠疟疾中的宿主防御:疟原虫感染导致巨噬细胞杀菌能力缺陷的分析。
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Studies on sporozoite-induced infections of rodent malaria. 3. The course of sporozoite-induced Plasmodium berghei in different hosts.子孢子诱导的啮齿类疟疾感染研究。3. 不同宿主中,子孢子诱导的伯氏疟原虫的病程。
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The chemotherapy of rodent malaria. IX. Causal prophylaxis. I. A method for demonstrating drug action on exo-erythrocytic stages.
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Effects of chloroquine, quinine, and cycloguanil upon the maturation of asexual erythrocytic forms of two strains of Plasmodium falciparum in vitro.氯喹、奎宁和环氯胍对两株恶性疟原虫无性红细胞内期形态体外成熟的影响。
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8
Stage-dependent inhibition of chloroquine on Plasmodium falciparum in vitro.氯喹对恶性疟原虫体外生长的阶段依赖性抑制作用
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9
Estimate of Plasmodium falciparum sporozoite content of Anopheles stephensi used to challenge human volunteers.用于感染人类志愿者的斯氏按蚊体内恶性疟原虫子孢子含量的估计。
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10
Safety and immunogenicity in man of a synthetic peptide malaria vaccine against Plasmodium falciparum sporozoites.一种针对恶性疟原虫子孢子的合成肽疟疾疫苗在人体中的安全性和免疫原性。
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接受氯喹治疗的志愿者中氯喹敏感型恶性疟原虫血症的持续情况。

Continuation of chloroquine-susceptible Plasmodium falciparum parasitemia in volunteers receiving chloroquine therapy.

作者信息

Murphy J R, Clyde D F, Herrington D A, Baqar S, Davis J R, Palmer K, Cortese J

机构信息

Department of Medicine, School of Medicine, University of Maryland, Baltimore 21201.

出版信息

Antimicrob Agents Chemother. 1990 Apr;34(4):676-9. doi: 10.1128/AAC.34.4.676.

DOI:10.1128/AAC.34.4.676
PMID:2188591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC171668/
Abstract

Volunteers infected with a chloroquine-susceptible line of Plasmodium falciparum were administered standard oral chloroquine therapy at the first detection of parasites in the blood. Parasitemias progressed in the face of therapy for up to 5 days and to levels up to 100-fold greater than those at the initiation of treatment. Thereafter, infections cleared without a requirement for additional chemotherapy. This course of infection and response to treatment has not been previously reported and may have been detected because volunteers were exposed to an unusually large number of sporozoites. The observations are consistent with the hypothesis that prolonged parasitemia resulted from the continued release of merozoites from liver.

摘要

感染对氯喹敏感的恶性疟原虫品系的志愿者在血液中首次检测到寄生虫时接受标准口服氯喹治疗。尽管进行了治疗,但寄生虫血症仍持续进展长达5天,且达到比治疗开始时高100倍的水平。此后,感染自行清除,无需额外化疗。此前尚未报道过这种感染过程和对治疗的反应,可能是因为志愿者接触了异常大量的子孢子才得以检测到。这些观察结果与以下假设一致,即长期寄生虫血症是由于裂殖子从肝脏持续释放所致。