Kamp Christel, Bornholdt Stefan
Institut für Theoretische Physik, Universität Kiel, Leibnizstrasse 15, 24098 Kiel, Germany.
Proc Biol Sci. 2002 Oct 7;269(1504):2035-40. doi: 10.1098/rspb.2002.2095.
The origin of the unusual incubation period distribution in the development of AIDS is largely unresolved. A key factor in understanding the observed distribution of latency periods, as well as the occurrence of infected individuals not developing AIDS at all, is the dynamics of the long-lasting struggle between HIV and the immune system. Using a computer simulation, we study the diversification of viral genomes under mutation and the selective pressure of the immune system. In non-HIV infections, vast spreading of viral genomes in genome space usually does not take place. In the case of an HIV infection, this may occur, as the virus successively weakens the immune system by the depletion of CD4+ cells. In a sequence space framework, this leads to a dynamically induced percolation transition, corresponding to the onset of AIDS. As a result, we obtain a prolonged shape of the incubation period distribution, as well as a finite fraction of non-progressors that do not develop AIDS, comparing well with results from recent clinical research.
艾滋病发展过程中异常潜伏期分布的起源在很大程度上尚未得到解决。理解观察到的潜伏期分布以及完全未发展为艾滋病的感染者出现情况的一个关键因素,是HIV与免疫系统之间长期斗争的动态过程。我们通过计算机模拟研究了在突变和免疫系统选择压力下病毒基因组的多样化。在非HIV感染中,病毒基因组在基因组空间中的广泛传播通常不会发生。在HIV感染的情况下,由于病毒通过消耗CD4+细胞相继削弱免疫系统,这种情况可能会发生。在序列空间框架中,这会导致动态诱导的渗流转变,对应于艾滋病的发病。结果,我们得到了潜伏期分布的延长形状,以及未发展为艾滋病的非进展者的有限比例,这与近期临床研究结果吻合良好。