Exploring the benefits of antibody immune response in HIV-1 infection using a discrete model

S. P. Showa;F. Nyabadza;S. D. Hove-Musekwa;G. Magombedze
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引用次数: 3

Abstract

The role of antibodies in HIV-1 infection is investigated using a discrete-time mathematical model that considers cell-free and cell-associated transmission of the virus. Model analysis shows that the effect of each type of antibody is dependent on the stage of the infection. Neutralizing antibodies are efficient in controlling the viral levels in the early days after seroconversion and antibodies that coat HIV-1-infected cells and recruit effector cells to either kill the HIV-1-infected cells or inhibit viral replication are efficient when the infection becomes established. Model simulations show that antibodies that inhibit viral replication are more effective in controlling the infection than those that recruit Natural Killer T cells after infection establishment. The model was fitted to subjects of the Tsedimoso study conducted in Botswana and conclusions similar to elasticity analysis results were obtained. Model fitting results predicted that neutralizing antibodies are more efficient in controlling the viral levels than antibodies that coat HIV-1-infected cells and recruit effector cells to either kill the HIV-1-infected cells or inhibit viral replication in the early days after seroconversion.
利用离散模型探索抗体免疫应答在HIV-1感染中的益处
使用离散时间数学模型研究抗体在HIV-1感染中的作用,该模型考虑了病毒的无细胞和细胞相关传播。模型分析表明,每种类型的抗体的效果取决于感染的阶段。中和抗体在血清转化后的早期有效控制病毒水平,当感染建立时,覆盖HIV-1感染细胞并募集效应细胞杀死HIV-1感染的细胞或抑制病毒复制的抗体是有效的。模型模拟表明,抑制病毒复制的抗体在控制感染方面比在感染建立后招募自然杀伤T细胞的抗体更有效。该模型适用于在博茨瓦纳进行的Tsedimoso研究的受试者,得出了与弹性分析结果相似的结论。模型拟合结果预测,中和抗体在控制病毒水平方面比包裹HIV-1感染细胞并募集效应细胞以杀死HIV-1感染的细胞或在血清转化后早期抑制病毒复制的抗体更有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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