Suppr超能文献

高通量筛选针对疟疾传播阶段为药物开发开辟了新途径。

A high-throughput screen targeting malaria transmission stages opens new avenues for drug development.

机构信息

Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.

出版信息

J Infect Dis. 2011 May 15;203(10):1445-53. doi: 10.1093/infdis/jir037.

Abstract

A major goal of the worldwide malaria eradication program is the reduction and eventual elimination of malaria transmission. All currently available antimalarial compounds were discovered on the basis of their activity against the asexually reproducing red blood cell stages of the parasite, which are responsible for the morbidity and mortality of human malaria. Resistance against these compounds is widespread, and there is an urgent need for novel approaches to reduce the emergence of resistance to new antimalarials as they are introduced. We have established and validated the first high-throughput assay targeting the red blood cell parasite stage required for transmission, the sexually reproducing gametocyte. This assay will permit identification of compounds specifically targeting the transmission stages in addition to the asexual stage parasites. Such stage-specific compounds may be used in a combination therapy, reducing the emergence of resistance by blocking transmission of resistant parasites that may be selected in a patient.

摘要

全球疟疾消除计划的主要目标是减少和最终消除疟疾传播。所有现有的抗疟化合物都是基于其对寄生虫无性繁殖的红细胞阶段的活性而被发现的,而寄生虫的无性繁殖的红细胞阶段是导致人类疟疾发病率和死亡率的原因。这些化合物已经广泛产生了抗药性,因此迫切需要新的方法来降低新抗疟药物出现抗药性的风险。我们已经建立并验证了第一个针对传播所需的红细胞寄生虫阶段(有性繁殖的配子体)的高通量检测方法。该检测方法将能够识别专门针对传播阶段的化合物,而不仅仅是针对无性阶段寄生虫的化合物。这种针对特定阶段的化合物可以用于联合治疗,通过阻止可能在患者中选择的耐药寄生虫的传播来减少耐药性的出现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3654/3080890/bd157d71d2b8/infdisjir037f01_3c.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验