Selection and quantification of infection endpoints for trials of vaccines against intestinal helminths

被引:12
作者
Alexander, Neal [1 ,2 ]
Cundill, Bonnie [1 ]
Sabatelli, Lorenzo [1 ]
Bethony, Jeffrey M. [2 ,3 ]
Diemert, David [2 ,4 ]
Hotez, Peter [2 ,4 ]
Smith, Peter G. [1 ]
Rodrigues, Laura C. [1 ]
Brooker, Simon [1 ]
机构
[1] Univ London London Sch Hyg & Trop Med, London WC1E 7HT, England
[2] George Washington Univ, Washington, DC USA
[3] Ctr Pesquisas Rene Rachou FIOCRUZ, Belo Horizonte, MG, Brazil
[4] Sabin Vaccine Inst, Washington, DC USA
基金
英国惠康基金;
关键词
Helminth vaccines; Parasitological endpoints; Mathematical model; SCHISTOSOMA-MANSONI; MALARIA VACCINE; POPULATION BIOLOGY; NECATOR-AMERICANUS; HOOKWORM; EFFICACY; COMMUNITY; CHILDREN; PATTERNS; DISEASE;
D O I
10.1016/j.vaccine.2011.03.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vaccines against human helminths are being developed but the choice of optimal parasitological endpoints and effect measures to assess their efficacy has received little attention. Assuming negative binomial distributions for the parasite counts, we rank the statistical power of three measures of efficacy: ratio of mean parasite intensity at the end of the trial, the odds ratio of infection at the end of the trial, and the rate ratio of incidence of infection during the trial. We also use a modelling approach to estimate the likely impact of trial interventions on the force of infection, and hence statistical power. We conclude that (1) final mean parasite intensity is a suitable endpoint for later phase vaccine trials, and (2) mass effects of trial interventions are unlikely to appreciably reduce the force of infection in the community - and hence statistical power - unless there is a combination of high vaccine efficacy and a large proportion of the population enrolled. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3686 / 3694
页数:9
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