Controlled Human Malaria Infection with Graded Numbers of Plasmodium falciparum NF135.C10-or NF166.C8-Infected Mosquitoes

被引:14
作者
Langenberg, Marijke C. C. [1 ,4 ]
Wammes, Linda J. [1 ,2 ]
McCall, Matthew B. B. [2 ,5 ,6 ]
Bijker, Else M. [3 ,7 ]
van Gemert, Geert-Jan [3 ]
Graumans, Wouter [3 ]
van de Vegte-Bolmer, Marga G. [3 ]
Teelen, Karina [3 ]
Hermsen, Cornelis C. [3 ]
Koelewijn, Rob [1 ,2 ]
van Hellemond, Jaap J. [2 ]
van Genderen, Perry J. J. [1 ]
Sauerwein, Robert W. [3 ]
机构
[1] Harbour Hosp, Inst Trop Dis, Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Med Microbiol & Infect Dis, Rotterdam, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Med Microbiol, Nijmegen, Netherlands
[4] Leiden Univ, Med Ctr, Dept Parasitol, Leiden, Netherlands
[5] Ctr Rech Med Lambarene, Libreville, Gabon
[6] Univ Tubingen, Inst Trop Med, Tubingen, Germany
[7] Radboud Univ Nijmegen, Med Ctr, Dept Paediat, Nijmegen, Netherlands
基金
比尔及梅琳达.盖茨基金会;
关键词
ANOPHELES-STEPHENSI; HUMAN VOLUNTEERS; CHALLENGE; EFFICACY; VACCINE; SPOROZOITES; SAFETY;
D O I
10.4269/ajtmh.18-0194
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Controlled human malaria infections (CHMIs) with Plasmodium falciparum (Pf) parasites are well established. Exposure to five Pf (NF54)-infected Anopheles mosquitoes results in 100% infection rates in malaria-naive volunteers. Recently Pf clones NF135.C10 and NF166.C8 were generated for application in CHMIs. Here, we tested the clinical infection rates of these clones, using graded numbers of Pf-infected mosquitoes. In a double-blind randomized trial, we exposed 24 malaria-naive volunteers to bites from one, two, or five mosquitoes infected with NF135.C10 or NF166.C8. The primary endpoint was parasitemia by quantitative polymerase chain reaction. For both strains, bites by five infected mosquitoes resulted in parasitemia in 4/4 volunteers; 3/4 volunteers developed parasitemia after exposure to one or two infected mosquitoes infected with either clone. The prepatent period was 7.25 +/- 4.0 days (median +/- range). There were no serious adverse events and comparable clinical symptoms between all groups. These data confirm the eligibility of NF135.C10 and NF166.C8 for use in CHMI studies.
引用
收藏
页码:709 / 712
页数:4
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