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人类免疫缺陷病毒(HIV)感染、高效抗逆转录病毒治疗(HAART)和丙型肝炎病毒(HCV)合并感染对血清白细胞介素-27 的影响。

Impact of HIV infection, highly active antiretroviral therapy, and hepatitis C coinfection on serum interleukin-27.

机构信息

Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.

出版信息

AIDS. 2010 Jun 1;24(9):1371-4. doi: 10.1097/QAD.0b013e3283391d2b.

DOI:10.1097/QAD.0b013e3283391d2b
PMID:20375875
Abstract

A newly described cytokine, interleukin-27 (IL-27), that activates naive CD4 T cells, has recently been shown to be an anti-HIV cytokine. However, the effect of HIV infection on IL-27 expression has not been characterized. We found that clinical characteristics, including HIV viral load, hepatitis C virus coinfection, and CD4 T cell counts, were associated with changes in serum IL-27. Overall, our results suggest circulating HIV may suppress IL-27, a critical concept in treatment development with this cytokine.

摘要

一种新描述的细胞因子白细胞介素-27(IL-27),能够激活初始 CD4 T 细胞,最近被证明是一种抗 HIV 的细胞因子。然而,HIV 感染对 IL-27 表达的影响尚未得到描述。我们发现,临床特征,包括 HIV 病毒载量、丙型肝炎病毒合并感染和 CD4 T 细胞计数,与血清 IL-27 的变化有关。总的来说,我们的结果表明,循环 HIV 可能抑制 IL-27,这是该细胞因子治疗开发中的一个关键概念。

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