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再感染阈值促进了结核病流行病学和疫苗效力的变异性。

The reinfection threshold promotes variability in tuberculosis epidemiology and vaccine efficacy.

作者信息

Gomes M Gabriela M, Franco Ana O, Gomes Manuel C, Medley Graham F

机构信息

Instituto Gulbenkian de Ciência, Apartado 14, 2781-901 Oeiras, Portugal.

出版信息

Proc Biol Sci. 2004 Mar 22;271(1539):617-23. doi: 10.1098/rspb.2003.2606.

Abstract

Population patterns of infection are determined largely by susceptibility to infection. Infection and vaccination induce an immune response that, typically, reduces susceptibility to subsequent infections. With a general epidemic model, we detect a 'reinfection threshold', above which reinfection is the principal type of transmission and, consequently, infection levels are much higher and vaccination fails. The model is further developed to address human tuberculosis (TB) and the impact of vaccination. The bacille Calmette-Guérin (BCG) is the only vaccine in current use against TB, and there is no consensus about its usefulness. Estimates of protection range from 0 to 80%, and this variability is aggravated by an association between low vaccine efficacy and high prevalence of the disease. We propose an explanation based on three postulates: (i) the potential for transmission varies between populations, owing to differences in socio-economic and environmental factors; (ii) exposure to mycobacteria induces an immune response that is partially protective against reinfection; and (iii) this protection is not significantly improved by BCG vaccination. These postulates combine to reproduce the observed trends, and this is attributed to a reinfection threshold intrinsic to the transmission dynamics. Finally, we demonstrate how reinfection thresholds can be manipulated by vaccination programmes, suggesting that they have a potentially powerful role in global control.

摘要

感染的人群模式很大程度上由对感染的易感性决定。感染和疫苗接种会引发免疫反应,通常会降低对后续感染的易感性。通过一个一般流行模型,我们检测到一个“再感染阈值”,高于此阈值,再感染是主要的传播类型,因此感染水平会高得多,疫苗接种也会失效。该模型进一步发展以解决人类结核病(TB)及疫苗接种的影响。卡介苗(BCG)是目前唯一用于预防结核病的疫苗,但其有效性尚无定论。保护效果的估计范围从0%到80%,而且这种变异性因疫苗效力低与疾病高流行率之间的关联而加剧。我们基于三个假设提出一种解释:(i)由于社会经济和环境因素的差异,不同人群之间的传播潜力有所不同;(ii)接触分枝杆菌会引发一种对再感染有部分保护作用的免疫反应;(iii)卡介苗接种并不能显著提高这种保护作用。这些假设共同作用再现了观察到的趋势,这归因于传播动力学固有的再感染阈值。最后,我们展示了如何通过疫苗接种计划来控制再感染阈值,表明它们在全球防控中可能发挥强大作用。

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