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Qualification of Standard Membrane-Feeding Assay with Plasmodium falciparum Malaria and Potential Improvements for Future Assays

机译:标准膜喂养试验与恶性疟并为未来的试验潜在的改进资质

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摘要

Vaccines that interrupt malaria transmission are of increasing interest and a robust functional assay to measure this activity would promote their development by providing a biologically relevant means of evaluating potential vaccine candidates. Therefore, we aimed to qualify the standard membrane-feeding assay (SMFA). The assay measures the transmission-blocking activity of antibodies by feeding cultured P. falciparum gametocytes to Anopheles mosquitoes in the presence of the test antibodies and measuring subsequent mosquito infection. The International Conference on Harmonisation (ICH) Harmonised Tripartite Guideline Q2(R1) details characteristics considered in assay validation. Of these characteristics, we decided to qualify the SMFA for Precision, Linearity, Range and Specificity. The transmission-blocking 4B7 monoclonal antibody was tested over 6 feeding experiments at several concentrations to determine four suitable concentrations that were tested in triplicate in the qualification experiments (3 additional feeds) to evaluate Precision, Linearity and Range. For Specificity, 4B7 was tested in the presence of normal mouse IgG. We determined intra- and inter-assay variability of % inhibition of mean oocyst intensity at each concentration of 4B7 (lower concentrations showed higher variability). We also showed that % inhibition was dependent on 4B7 concentration and the activity is specific to 4B7. Since obtaining empirical data is time-consuming, we generated a model using data from all 9 feeds and simulated the effects of different parameters on final readouts to improve the assay procedure and analytical methods for future studies. For example, we estimated the effect of number of mosquitoes dissected on variability of % inhibition, and simulated the relationship between % inhibition in oocyst intensity and % inhibition of prevalence of infected mosquitos at different mean oocysts in the control. SMFA is one of the few biological assays used in preclinical and early clinical development of transmission-blocking vaccines, and this study strongly supports its further development and application.
机译:中断疟疾传播的疫苗受到越来越多的关注,通过提供生物学上相关的评估潜在疫苗候选者的手段,一种用于测量这种活性的功能强大的测定方法将促进其发展。因此,我们的目标是使标准的膜进食分析(SMFA)合格。该测定法通过在存在测试抗体的情况下将培养的恶性疟原虫配子细胞喂食按蚊来测量抗体的传递阻断活性,并测量随后的蚊子感染。国际协调会议(ICH)协调三方指南Q2(R1)详细介绍了分析验证中考虑的特征。在这些特征中,我们决定使SMFA的精度,线性,范围和特异性合格。在6个饲喂实验中以几种浓度测试了阻断传输的4B7单克隆抗体,以确定四个合适的浓度,在资格实验中一式三份地对其进行了测试(另外3种饲料),以评估精密度,线性和范围。对于特异性,在正常小鼠IgG存在下测试4B7。我们确定了在每种浓度的4B7时平均卵囊强度抑制百分比的测定内和测定间变异性(较低的浓度显示较高的变异性)。我们还显示抑制百分比取决于4B7浓度,且活性对4B7具有特异性。由于获取经验数据非常耗时,因此我们使用来自所有9种饲料的数据生成了一个模型,并模拟了不同参数对最终读数的影响,以改进测定程序和分析方法,以供将来研究。例如,我们估算了解剖的蚊子数量对抑制百分率变异性的影响,并模拟了对照组中不同平均卵囊内卵囊强度的百分抑制与感染蚊子患病率的百分抑制之间的关系。 SMFA是在临床上和早期临床上用于传播阻断疫苗的少数生物学检测方法之一,这项研究强烈支持其进一步的开发和应用。

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