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Estimating the infectivity of CCR5-tropic simian immunodeficiency virus SIV(mac251) in the gut

机译:估计CCR5-tropic猴的传染性免疫缺陷病毒SIV (mac251)在肠道

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CD4+ T-cell depletion during acute human immunodeficiency virus infection occurs predominantly in the gastrointestinal mucosa. Using experimental data on SIV(mac251) viral load in blood and CD4+ T cells in the jejunum, we modeled the kinetics of CD4+ T-cell infection and death and estimated the viral infectivity. The infectivity of SIV(mac251) is higher than previously estimated for SHIV89.6P infection, but this higher infectivity is offset by a lower average peak viral load in SIV(mac251). Thus, the dynamics of target cell infection and death are remarkably similar between a CXCR4- and a CCR5-tropic infection in vivo.
机译:在人类急性CD4 + t细胞耗竭免疫缺陷病毒感染发生主要在胃肠道黏膜。利用实验数据对SIV病毒载量(mac251)在血液和CD4 + T细胞在空肠,我们CD4 + t细胞感染和动力学建模死亡和估计病毒传染性。猴免疫缺陷病毒的传染性(mac251)高于之前估计SHIV89.6P感染,但是这种高传染性抵消较低平均峰值在SIV病毒载量(mac251)。动态目标细胞感染和死亡趋化因子受体CXCR4和之间非常相似CCR5-tropic感染体内。

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