Weber A, Weber M, Milligan P
Institut für Informatik II, Universität Bonn, Römerstrasse 164, 53117 Bonn, Germany.
Math Biosci. 2001 Aug;172(2):95-113. doi: 10.1016/s0025-5564(01)00066-9.
Respiratory syncytial virus (RSV) is the most common cause of acute lower respiratory tract infection in children. In this paper we use models of RSV transmission to interpret the pattern of seasonal epidemics of RSV disease observed in different countries, and to estimate epidemic and eradication thresholds for RSV infection. We compare the standard SIRS model with a more realistic model of RSV transmission in which individuals acquire immunity gradually after repeated exposure to infection. The models are fitted to series of monthly hospital case reports of RSV disease from developed and developing countries. The models can explain many of the observed patterns: regular yearly outbreaks in some countries, and in other countries cycles of alternating larger and smaller annual epidemics, with shifted maxima in alternate years. Previously these patterns have been attributed to the transmission of different strains of RSV. In some countries the timing of epidemics is not consistent with increased social contact among school children during term time being the major driving mechanism. Climatic factors appear to be more important. Qualitatively different models gave equally good fits to the data series, but estimates of the transmission parameter were different by a factor of 4. Estimates of the basic reproduction number (R(0)) ranged from 1.2 to 2.1 with the SIRS model, and from 5.4 to 7.1 with the model with gradual acquisition of partial immunity.
呼吸道合胞病毒(RSV)是儿童急性下呼吸道感染最常见的病因。在本文中,我们使用RSV传播模型来解释在不同国家观察到的RSV疾病季节性流行模式,并估计RSV感染的流行阈值和根除阈值。我们将标准的SIRS模型与一个更现实的RSV传播模型进行比较,在这个模型中,个体在反复接触感染后逐渐获得免疫力。这些模型与来自发达国家和发展中国家的RSV疾病月度医院病例报告系列进行拟合。这些模型可以解释许多观察到的模式:一些国家每年定期爆发,而在其他国家,年度流行呈现大小交替的周期,且交替年份的最大值有所偏移。以前,这些模式被归因于不同毒株的RSV传播。在一些国家,疫情发生的时间与学期期间学龄儿童社交接触增加作为主要驱动机制不一致。气候因素似乎更为重要。定性不同的模型对数据系列的拟合效果同样良好,但传播参数的估计相差4倍。使用SIRS模型时,基本再生数(R(0))的估计范围为1.2至2.1,而使用逐渐获得部分免疫力的模型时,估计范围为5.4至7.1。