人类免疫缺陷病毒疾病进展的自身抗原预后

C. Bristow, Hirenkumar Patel, R. Arnold
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引用次数: 20

摘要

我们最近发现了一种细胞外蛋白α1蛋白酶抑制剂(α1PI;α1抗胰蛋白酶)是体外人类免疫缺陷病毒(HIV)感染性结果所必需的。我们在一项hiv血清阳性患者的研究中表明,病毒载量的降低与循环α1PI的降低显著相关。在无症状的HIV疾病类别中,100%的患者表现出活性α1PI水平不足,这种情况已知会导致肺部退行性疾病和寿命急剧缩短。此外,hiv相关的α1PI缺乏与循环抗α1PI免疫球蛋白g相关。这些结果表明,预防hiv相关的α1PI缺乏可能为预防hiv相关的病理生理提供了一个战略靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self Antigen Prognostic for Human Immunodeficiency Virus Disease Progression
ABSTRACT We have recently found that an extracellular protein, α1 proteinase inhibitor (α1PI; α1 antitrypsin), is required for in vitro human immunodeficiency virus (HIV) infectivity outcome. We show here in a study of HIV-seropositive patients that decreased viral load is significantly correlated with decreased circulating α1PI. In the asymptomatic category of HIV disease, 100% of patients manifest deficient levels of active α1PI, a condition known to lead to degenerative lung diseases and a dramatically reduced life span. Further, HIV-associated α1PI deficiency is correlated with circulating anti-α1PI immunoglobulin G. These results suggest that preventing HIV-associated α1PI deficiency may provide a strategic target for preventing HIV-associated pathophysiology.
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