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人类免疫缺陷病毒/获得性免疫缺陷综合征:从数学角度看待药物使用

Human immunodeficiency virus/acquired immune deficiency syndrome: Using drug from mathematical perceptive.

作者信息

Chatterjee Amar Nath, Saha Shubhankar, Roy Priti Kumar

机构信息

Amar Nath Chatterjee, Shubhankar Saha, Priti Kumar Roy, Centre for Mathematical Biology and Ecology, Department of Mathematics, Jadavpur University, Kolkata 700032, India.

出版信息

World J Virol. 2015 Nov 12;4(4):356-64. doi: 10.5501/wjv.v4.i4.356.

Abstract

Entry of acquired immune deficiency syndrome virus into the host immune cell involves the participation of various components of host and viral cell unit. These components may be categorized as attachment of the viral surface envelope protein subunit, gp120, to the CD4(+) receptor and chemokine coreceptors, CCR5 and CXCR4, present on T cell surface. The viral fusion protein, gp41, the second cleaved subunit of Env undergoes reconfiguration and the membrane fusion reaction itself. Since the CD4(+) T cell population is actively involved; the ultimate outcome of human immunodeficiency virus infection is total collapse of the host immune system. Mathematical modeling of the stages in viral membrane protein-host cell receptor-coreceptor interaction and the effect of antibody vaccine on the viral entry into the susceptible host cell has been carried out using as impulsive differential equations. We have studied the effect of antibody vaccination and determined analytically the threshold value of drug dosage and dosing interval for optimum levels of infection. We have also investigated the effect of perfect adherence of drug dose on the immune cell count in extreme cases and observed that systematic drug dosage of the immune cells leads to longer and improved lives.

摘要

获得性免疫缺陷综合征病毒进入宿主免疫细胞涉及宿主和病毒细胞单元的各种成分的参与。这些成分可分为病毒表面包膜蛋白亚基gp120与T细胞表面存在的CD4(+)受体以及趋化因子共受体CCR5和CXCR4的附着。病毒融合蛋白gp41是Env的第二个裂解亚基,会发生重新构型以及膜融合反应本身。由于CD4(+) T细胞群体积极参与其中,人类免疫缺陷病毒感染的最终结果是宿主免疫系统完全崩溃。已使用脉冲微分方程对病毒膜蛋白-宿主细胞受体-共受体相互作用阶段以及抗体疫苗对病毒进入易感宿主细胞的影响进行了数学建模。我们研究了抗体疫苗接种的效果,并通过分析确定了达到最佳感染水平的药物剂量和给药间隔的阈值。我们还研究了在极端情况下药物剂量的完美依从性对免疫细胞计数的影响,并观察到对免疫细胞进行系统的药物给药可延长生命并改善生活质量。

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本文引用的文献

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Antibodies in HIV-1 vaccine development and therapy.HIV-1 疫苗开发和治疗中的抗体。
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J Theor Biol. 2008 Mar 21;251(2):227-37. doi: 10.1016/j.jtbi.2007.11.032. Epub 2007 Dec 3.
10
Dynamics of HIV infection of CD4+ T cells.CD4+ T细胞的HIV感染动态
Math Biosci. 1993 Mar;114(1):81-125. doi: 10.1016/0025-5564(93)90043-a.

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