伯氏疟原虫
间日疟原虫
病毒学
离体
生物
疟原虫(生命周期)
顶复亚门
阻塞(统计)
疟疾
体内
传输(电信)
免疫学
恶性疟原虫
寄生虫寄主
遗传学
统计
电气工程
工程类
万维网
计算机科学
数学
作者
Yi Cao,Clifford T. H. Hayashi,Nirbhay Kumar
标识
DOI:10.1093/infdis/jiae102
摘要
Plasmodium falciparum and Plasmodium vivax account for >90% global malaria burden. Transmission intervention strategies encompassing transmission-blocking vaccines (TBV) and drugs represent ideal public health tools to eliminate malaria at the population level. The availability of mature P. falciparum gametocytes through in vitro culture has facilitated development of a standard membrane feeding assay to assess efficacy of transmission interventions against P. falciparum. The lack of in vitro culture for P. vivax has significantly hampered similar progress on P. vivax and limited studies have been possible using blood from infected patients in endemic areas. The ethical and logistical limitations of on-time access to blood from patients have impeded the development of P. vivax TBVs.
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