McKenzie F E, Bossert W H
Department of Organismic and Evolutionary Biology and the Division of Applied Sciences, Harvard University, 33 Oxford Street, Cambridge, MA 02138, USA.
J Theor Biol. 1997 Sep 7;188(1):127-40. doi: 10.1006/jtbi.1997.0478.
We develop a system of ordinary differential equations to model the dynamics of the blood-stages of the malaria parasite, Plasmodium falciparum. Variants of the model allow the study of a set of hypotheses about the interaction of the parasite with the host immune system, in particular with regard to the stimulation of the immune response and the regulation of the rate of conversion from the pathogenic, asexual to the transmissible, sexual blood stage. The values of several parameters of our models can be estimated from previous empirical work. Although the dynamics of the variants differ somewhat, in each variant some set of values of the three unconstrained parameters, different from one variant to the next, produces a range of behaviours quantitatively consistent with those reported from clinical studies. Some parameter values produce infections which quickly terminate, while others approach a chronic equilibrium level or produce oscillations, with repeated severe peaks separated by periods of undetectable parasitemia. We examine these and several other distinctions that might be used to assess model variants and focus further empirical research.
我们开发了一个常微分方程系统,以模拟恶性疟原虫血液阶段的动态变化。该模型的变体允许研究一组关于寄生虫与宿主免疫系统相互作用的假设,特别是关于免疫反应的刺激以及从致病的无性血液阶段向可传播的有性血液阶段转化率的调节。我们模型的几个参数值可以从以前的实证研究中估计出来。尽管各变体的动态变化有所不同,但在每个变体中,三个无约束参数的某些值集(各变体不同)会产生一系列行为,在数量上与临床研究报告的行为一致。一些参数值会导致感染迅速终止,而其他参数值会使感染接近慢性平衡水平或产生振荡,反复出现严重峰值,中间间隔不可检测的寄生虫血症期。我们研究了这些以及其他一些可能用于评估模型变体并进一步聚焦实证研究的差异。