A mathematical model for HIV dynamics with multiple infections: implications for immune escape.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-05-19 DOI:10.1007/s00285-024-02104-w
Qi Deng, Ting Guo, Zhipeng Qiu, Yuming Chen
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Abstract

Multiple infections enable the recombination of different strains, which may contribute to viral diversity. How multiple infections affect the competition dynamics between the two types of strains, the wild and the immune escape mutant, remains poorly understood. This study develops a novel mathematical model that includes the two strains, two modes of viral infection, and multiple infections. For the representative double-infection case, the reproductive numbers are derived and global stabilities of equilibria are obtained via the Lyapunov direct method and theory of limiting systems. Numerical simulations indicate similar viral dynamics regardless of multiplicities of infections though the competition between the two strains would be the fiercest in the case of quadruple infections. Through sensitivity analysis, we evaluate the effect of parameters on the set-point viral loads in the presence and absence of multiple infections. The model with multiple infections predict that there exists a threshold for cytotoxic T lymphocytes (CTLs) to minimize the overall viral load. Weak or strong CTLs immune response can result in high overall viral load. If the strength of CTLs maintains at an intermediate level, the fitness cost of the mutant is likely to have a significant impact on the evolutionary dynamics of mutant viruses. We further investigate how multiple infections alter the viral dynamics during the combination antiretroviral therapy (cART). The results show that viral loads may be underestimated during cART if multiple-infection is not taken into account.

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艾滋病病毒多重感染动态数学模型:对免疫逃逸的影响。
多重感染使不同毒株得以重组,这可能有助于病毒的多样性。人们对多重感染如何影响野生毒株和免疫逃逸突变株这两种毒株之间的竞争动态仍然知之甚少。本研究建立了一个新的数学模型,其中包括两种毒株、两种病毒感染模式和多重感染。对于具有代表性的双重感染情况,通过 Lyapunov 直接法和极限系统理论推导出了繁殖数,并获得了平衡态的全局稳定性。数值模拟结果表明,尽管在四重感染的情况下,两种病毒株之间的竞争最为激烈,但无论感染的多重性如何,病毒的动态都是相似的。通过敏感性分析,我们评估了存在和不存在多重感染时参数对设定点病毒载量的影响。有多重感染的模型预测,细胞毒性 T 淋巴细胞(CTL)存在一个阈值,可将总体病毒载量降至最低。细胞毒性 T 淋巴细胞免疫反应的强弱会导致总体病毒载量的高低。如果 CTLs 的强度维持在中间水平,突变体的适应性成本很可能会对突变病毒的进化动态产生重大影响。我们进一步研究了多重感染如何改变联合抗逆转录病毒疗法(cART)期间的病毒动态。结果表明,如果不考虑多重感染,在 cART 期间病毒载量可能会被低估。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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