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Low immune activation despite high levels of pathogenic human immunodeficiency virus type 1 results in long-term asymptomatic disease

机译:尽管1型致病性人类免疫缺陷病毒水平高,但免疫激活仍较低,可导致长期无症状疾病

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摘要

Long-term asymptomatic human immunodeficiency virus (HIV)-infected individuals (LTA) usually have low viral load and low immune activation. To discern whether viral load or immune activation is dominant in determining progression to AIDS, we studied three exceptional LTA with high viral loads. HIV type 1 isolates from these LTA were as pathogenic as viruses from progressors in organ culture. Despite high viral loads, these LTA had low levels of proliferating and activated T cells compared to progressors, like other LTA. In contrast to those in progressors, HIV-specific CD4(+) T-cell responses in these LTA were maintained. Thus, low immune activation despite a high viral load preserved HIV-specific T-cell responses and resulted in a long-term asymptomatic phenotype
机译:长期无症状人类免疫缺陷病毒(HIV)感染的个体(LTA)通常具有低病毒载量和低免疫激活。为了辨别病毒载量或免疫激活是决定艾滋病进展的主要因素,我们研究了三种例外的高病毒载量LTA。来自这些LTA的HIV 1型分离株与来自器官培养中的进展者的病毒一样具有致病性。尽管病毒载量很高,但与其他LTA一样,这些LTA的增殖和活化T细胞水平却较低。与那些进行中的人相反,这些LTA中的HIV特异性CD4(+)T细胞反应得以维持。因此,尽管病毒载量高,但免疫激活仍低,可保留HIV特异性T细胞反应并导致长期无症状表型

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