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CD4+ T细胞亚群的HIV感染建模。

Modeling HIV infection of CD4+ T-cell subpopulations.

作者信息

Essunger P, Perelson A S

机构信息

Theoretical Division, Los Alamos National Laboratory, NM 87545.

出版信息

J Theor Biol. 1994 Oct 21;170(4):367-91. doi: 10.1006/jtbi.1994.1199.

Abstract

We develop and analyze a set of models for the interaction of HIV with CD4+ T cells. We consider three major subpopulations of T cells: virgin, activated and memory. In our first model we assume that HIV can infect activated cells but not resting cells. We then generalize the model to take into account recent reports that HIV can enter resting cells but that such entry does not lead to the production of completely reverse transcribed copies of the viral genome or integration of the DNA copy into the host cell's genome unless cell activation occurs. Our models show that T-cell memory is greatly reduced by HIV infection and that T-cell depletion may be due to the direct killing of peripheral T cells and T-cell precursors in the thymus.

摘要

我们开发并分析了一组关于HIV与CD4+ T细胞相互作用的模型。我们考虑T细胞的三个主要亚群:初始T细胞、活化T细胞和记忆T细胞。在我们的第一个模型中,我们假设HIV能够感染活化细胞,但不能感染静息细胞。随后,我们对该模型进行了推广,以考虑到最近的报道,即HIV能够进入静息细胞,但这种进入不会导致产生病毒基因组的完全逆转录拷贝,也不会导致DNA拷贝整合到宿主细胞基因组中,除非细胞发生活化。我们的模型表明,HIV感染会大大降低T细胞记忆,并且T细胞耗竭可能是由于外周T细胞和胸腺中的T细胞前体被直接杀伤所致。

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