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经无菌斯蒂芬斯按蚊叮咬感染恶性疟原虫疟疾挑战:一项随机感染性试验结果。

Plasmodium falciparum malaria challenge by the bite of aseptic Anopheles stephensi mosquitoes: results of a randomized infectivity trial.

机构信息

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.

出版信息

PLoS One. 2010 Oct 21;5(10):e13490. doi: 10.1371/journal.pone.0013490.

DOI:10.1371/journal.pone.0013490
PMID:21042404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2958836/
Abstract

BACKGROUND

Experimental infection of malaria-naïve volunteers by the bite of Plasmodium falciparum-infected mosquitoes is a preferred means to test the protective effect of malaria vaccines and drugs. The standard model relies on the bite of five infected mosquitoes to induce malaria. We examined the efficacy of malaria transmission using mosquitoes raised aseptically in compliance with current Good Manufacturing Practices (cGMPs).

METHODS AND FINDINGS

Eighteen adults aged 18-40 years were randomized to receive 1, 3 or 5 bites of Anopheles stephensi mosquitoes infected with the chloroquine-sensitive NF54 strain of P. falciparum. Seventeen participants developed malaria; fourteen occurring on Day 11. The mean prepatent period was 10.9 days (9-12 days). The geometric mean parasitemia was 15.7 parasites/µL (range: 4-70) by microscopy. Polymerase chain reaction (PCR) detected parasites 3.1 (range: 0-4) days prior to microscopy. The geometric mean sporozoite load was 16,753 sporozoites per infected mosquito (range: 1,000-57,500). A 1-bite participant withdrew from the study on Day 13 post-challenge and was PCR and smear negative.

CONCLUSIONS

The use of aseptic, cGMP-compliant P. falciparum-infected mosquitoes is safe, is associated with a precise prepatent period compared to the standard model and appears more efficient than the standard approach, as it led to infection in 100% (6/6) of volunteers exposed to three mosquito bites and 83% (5/6) of volunteers exposed to one mosquito bite.

TRIAL REGISTRATION

ClinicalTrials.gov NCT00744133.

摘要

背景

通过感染疟原虫的蚊子叮咬疟原虫感染的疟疾初治志愿者,是一种检测疟疾疫苗和药物保护效果的首选方法。标准模型依赖于五只受感染蚊子的叮咬来诱发疟疾。我们研究了使用符合现行良好生产规范(cGMP)的无菌方法饲养的蚊子进行疟疾传播的效果。

方法和发现

18 名年龄在 18-40 岁的成年人被随机分配接受 1、3 或 5 次感染氯喹敏感 NF54 株疟原虫的按蚊叮咬。17 名参与者出现疟疾,其中 14 名发生在第 11 天。平均潜伏期为 10.9 天(9-12 天)。显微镜下的几何平均疟原虫密度为 15.7 个/µL(范围:4-70)。聚合酶链反应(PCR)在显微镜检查前 3.1 天(范围:0-4)检测到寄生虫。每只受感染蚊子的几何平均孢子虫载量为 16,753 个孢子虫(范围:1,000-57,500)。一名 1 次叮咬的参与者在挑战后第 13 天退出研究,PCR 和涂片均为阴性。

结论

使用无菌、符合 cGMP 的疟原虫感染蚊子是安全的,与标准模型相比具有精确的潜伏期,并且似乎比标准方法更有效,因为它导致 100%(6/6)暴露于 3 次蚊子叮咬的志愿者和 83%(5/6)暴露于 1 次蚊子叮咬的志愿者感染。

试验注册

ClinicalTrials.gov NCT00744133。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0715/2958836/d00b9994b1ee/pone.0013490.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0715/2958836/d00b9994b1ee/pone.0013490.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0715/2958836/d00b9994b1ee/pone.0013490.g003.jpg

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