Zorzenon dos Santos R M, Coutinho S
Instituto de Física de São Carlos, Universidade de SãoPaulo, CP 369, CEP 13560-970, São Carlos, São Paulo, Brazil.
Phys Rev Lett. 2001 Oct 15;87(16):168102. doi: 10.1103/PhysRevLett.87.168102. Epub 2001 Sep 26.
We use a cellular automata model to study the evolution of human immunodeficiency virus (HIV) infection and the onset of acquired immunodeficiency syndrome (AIDS). The model takes into account the global features of the immune response to any pathogen, the fast mutation rate of the HIV, and a fair amount of spatial localization, which may occur in the lymph nodes. Our results reproduce the three-phase pattern observed in T cell and virus counts of infected patients, namely, the primary response, the clinical latency period, and the onset of AIDS. The dynamics of real experimental data is related to the transient behavior of our model and not to its steady state. We have also found that the infected cells organize themselves into spatial structures, which are responsible for the decrease on the concentration of uninfected cells, leading to AIDS.
我们使用细胞自动机模型来研究人类免疫缺陷病毒(HIV)感染的演变以及获得性免疫缺陷综合征(AIDS)的发病情况。该模型考虑了针对任何病原体的免疫反应的全局特征、HIV的快速突变率以及可能在淋巴结中发生的相当程度的空间定位。我们的结果再现了在感染患者的T细胞和病毒计数中观察到的三个阶段模式,即初始反应、临床潜伏期和AIDS的发病。实际实验数据的动态变化与我们模型的瞬态行为相关,而非其稳态。我们还发现,受感染细胞会自行组织成空间结构,这些结构导致未感染细胞浓度降低,进而引发AIDS。