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首页> 外文期刊>Virology >Analysis of cellular factors influencing the replication of humanimmunodeficiency virus type I in human macrophages derived from blood ofdifferent healthy donors
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Analysis of cellular factors influencing the replication of humanimmunodeficiency virus type I in human macrophages derived from blood ofdifferent healthy donors

机译:影响不同健康供体血液来源的人巨噬细胞中I型人免疫缺陷病毒复制的细胞因子分析

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摘要

We analyzed parameters influencing HIV-1 infectibility of cells of the monocyte/macrophage lineage (MO/MAC) isolated from different healthy donors. The proportion of in vitro-infected cells and replication kinetics in different donor MAC ranged from 0.03 to 99% p24 antigen-positive MAC and from undetectable RT activity up to 5 x 10(6) cpm/ml/90 min, respectively. As a quantitative measurement for HIV-1 susceptibility of donor MO/MAC, we determined TCID50 values of defined virus stocks which varied up to 3000-fold depending on the donor MAC used for titration. As host factors which may influence the viral infection we determined the expression of Virus receptors CD4, CCR5, CXCR4, and CCR3 as well as the secretion of the natural ligands of CCR5, which altogether showed no correlation with HIV-1 infectibility of the cells. Moreover, other MO-derived secretory factors which might affect viral infection of these cells could be excluded. Furthermore, expression of maturation-related antigens CD14, CD16, HLA-DR, and MAX.1/CPM was determined. Analysis of the reverse transcription process revealed that restricted HIV-1 infection was reflected by highly reduced or even undetectable full-length HIV-1 DNA formation, although early and intermediate transcripts appeared, suggesting that viral replication is blocked after entry at the level of early reverse transcription,
机译:我们分析了影响从不同健康供体分离的单核细胞/巨噬细胞谱系(MO / MAC)细胞的HIV-1感染性的参数。不同供体MAC中体外感染细胞的比例和复制动力学分别为0.03至99%p24抗原阳性MAC,以及高达5 x 10(6)cpm / ml / 90分钟的无法检测到的RT活性。作为对捐献者MO / MAC的HIV-1敏感性的定量测量,我们确定了确定的病毒原种的TCID50值,根据所滴定的捐献者MAC的不同,其变异高达3000倍。作为可能影响病毒感染的宿主因素,我们确定了病毒受体CD4,CCR5,CXCR4和CCR3的表达以及CCR5天然配体的分泌,这与细胞的HIV-1感染性无关。而且,可以排除可能影响这些细胞的病毒感染的其他MO来源的分泌因子。此外,确定了成熟相关抗原CD14,CD16,HLA-DR和MAX.1 / CPM的表达。对逆转录过程的分析表明,尽管出现了早期和中期转录本,但HIV-1感染受到限制的情况是通过高度减少甚至无法检测到的全长HIV-1 DNA形成反映出来的,这表明病毒的复制在进入早期水平后被阻断了。反转录

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