Institute of Physiology 2, Universitätsklinikum, Friedrich Schiller University, 07743 Jena, Germany.
Department of Bioinformatics, Friedrich Schiller University, 07743 Jena, Germany.
J R Soc Interface. 2018 May;15(142). doi: 10.1098/rsif.2017.0963.
As a part of the complement system, factor H regulates phagocytosis and helps differentiate between a body's own and foreign cells. Owing to mimicry efforts, some pathogenic microorganisms such as are able to bind factor H on their cell surfaces and, thus, become similar to host cells. This implies that the decision between self and foreign is not clear-cut, which leads to a classification problem for the immune system. Here, two different alleles determining the binding affinity of factor H are relevant. Those alleles differ in the SNP Y402H; they are known to be associated with susceptibility to certain diseases. Interestingly, the fraction of both alleles differs in ethnic groups. The game-theoretical model proposed in this article explains the coexistence of both alleles by a game and investigates the trade-off between pathogen detection and protection of host cells. Further, we discuss the ethnicity-dependent frequencies of the alleles. Moreover, the model elucidates the mimicry efforts by pathogenic microorganisms.
作为补体系统的一部分,因子 H 调节吞噬作用,并有助于区分自身和外来细胞。由于模拟作用,一些病原微生物,如 ,能够在其细胞表面结合因子 H,从而变得类似于宿主细胞。这意味着自身和外来之间的区别并不明显,这导致免疫系统面临分类问题。在这里,两个不同的等位基因决定了因子 H 的结合亲和力,这两个等位基因在 SNP Y402H 上有所不同;已知它们与某些疾病的易感性有关。有趣的是,这两个等位基因的比例在不同的族群中有所不同。本文提出的博弈论模型通过博弈来解释这两个等位基因的共存,并研究了病原体检测和宿主细胞保护之间的权衡。此外,我们还讨论了等位基因的族群依赖性频率。此外,该模型阐明了病原微生物的模拟作用。