Wodarz D, Nowak M A
Department of Zoology, University of Oxford, UK.
Proc Biol Sci. 1998 Nov 22;265(1411):2149-58. doi: 10.1098/rspb.1998.0552.
We use mathematical models to determine possible mechanisms contributing to the evolution and rise of virulent CXCR4-tropic HIV in vivo. The models predict that the ability of the virus to specialize on a given target cell type depends on the exact fitness landscape of the viral mutants. Because this fitness landscape varies between people, this may explain why the evolution of fully CXCR4-tropic strains only occurs in about 50% of infected patients. Assuming that CXCR4-tropic HIV may evolve, we investigate the effect of different immune responses on the rise of such virulent strains. If we assume that CXCR4-tropic HIV is more cytopathic than CCR5-tropic virus, virulent CXCR4-tropic mutants remain suppressed at low levels both in the absence of an immune response, and in the presence of responses that act on the virus before integration into the host genome. On the other hand, this difference in cytopathogenicity is reduced by the presence of immune responses acting on infected cells, allowing CXCR4-tropic HIV to coexist with the CCR5-tropic virus. These results may help to interpret experimental data and are discussed with reference to the literature.
我们使用数学模型来确定促成体内毒性CXCR4嗜性HIV进化和出现的可能机制。这些模型预测,病毒在特定靶细胞类型上专门化的能力取决于病毒突变体的确切适应度格局。由于这种适应度格局因人而异,这或许可以解释为何完全CXCR4嗜性毒株的进化仅在约50%的感染患者中发生。假设CXCR4嗜性HIV可能进化,我们研究不同免疫反应对这类毒性毒株出现的影响。如果我们假设CXCR4嗜性HIV比CCR5嗜性病毒更具细胞病变性,那么在没有免疫反应以及在病毒整合入宿主基因组之前对病毒起作用的反应存在的情况下,毒性CXCR4嗜性突变体均会在低水平受到抑制。另一方面,作用于受感染细胞的免疫反应的存在会降低这种细胞病变性差异,从而使CXCR4嗜性HIV能够与CCR5嗜性病毒共存。这些结果可能有助于解释实验数据,并会结合文献进行讨论。