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清除耐药疟原虫作为恶性疟原虫疟疾保护性免疫的模型。

Clearance of drug-resistant parasites as a model for protective immunity in Plasmodium falciparum malaria.

作者信息

Djimdé Abdoulaye A, Doumbo Ogobara K, Traore Ousmane, Guindo Ando B, Kayentao Kassoum, Diourte Yacouba, Niare-Doumbo Safiatou, Coulibaly Drissa, Kone Abdoulaye K, Cissoko Yacouba, Tekete Mamadou, Fofana Bakary, Dicko Alassane, Diallo Dapa A, Wellems Thomas E, Kwiatkowski Dominic, Plowe Christopher V

机构信息

Bandiagara Malaria Project, Malaria Research and Training Center, Department of Epidemiology of Parasitic Diseases, Faculty of Medicine, Pharmacy and Dentistry, University of Bamako, Bamako, Mali.

出版信息

Am J Trop Med Hyg. 2003 Nov;69(5):558-63.

Abstract

Residents of malaria-endemic areas sometimes spontaneously clear Plasmodium falciparum infection without drug treatment, implying an important role for host factors such as immunity in this clearance. Host factors may also contribute to clearance of parasites resistant to a treatment drug. Chloroquine resistance is caused by point mutations in P. falciparum chloroquine resistance transporter (pfcrt) gene. We investigated the clearance of malaria parasites carrying the key chloroquine resistance-conferring PfCRT mutation K76T in patients treated with chloroquine. We found that the ability to clear these resistant parasites is strongly dependent on age (the best surrogate for protective immunity in endemic areas), suggesting that host immunity plays a critical role in the clearance of resistant P. falciparum infections. Age-adjusted comparison of subjects able to clear resistant parasites and those unable to do so provides a new phenotype for identifying host immune and genetic factors responsible for protective immunity against malaria.

摘要

疟疾流行地区的居民有时在未经药物治疗的情况下能自发清除恶性疟原虫感染,这意味着宿主因素(如免疫力)在这种清除过程中发挥着重要作用。宿主因素也可能有助于清除对治疗药物耐药的寄生虫。氯喹耐药性是由恶性疟原虫氯喹耐药转运蛋白(pfcrt)基因的点突变引起的。我们研究了在用氯喹治疗的患者中携带关键氯喹耐药性赋予突变PfCRT K76T的疟原虫的清除情况。我们发现清除这些耐药寄生虫的能力强烈依赖于年龄(这是流行地区保护性免疫力的最佳替代指标),这表明宿主免疫力在清除耐药恶性疟原虫感染中起着关键作用。对能够清除耐药寄生虫的受试者和不能清除耐药寄生虫的受试者进行年龄调整后的比较,为识别负责疟疾保护性免疫的宿主免疫和遗传因素提供了一种新的表型。

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