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丙型肝炎病毒基因型与HIV合并感染会影响未受刺激的外周血单核细胞中的细胞因子mRNA水平,但不会改变T1/T2平衡。

Hepatitis C virus genotype and HIV coinfection affect cytokine mRNA levels in unstimulated PBMC but do not shift the T1/T2 balance.

作者信息

Lee Silvia, Watson Mark W, Clark Ben, Flexman James P, Cheng Wendy, French Martyn A H, Price Patricia

机构信息

Department of Clinical Immunology and Biochemical Genetics, Royal Perth Hospital, Perth, Western Australia, Australia.

出版信息

Immunol Cell Biol. 2006 Aug;84(4):390-5. doi: 10.1111/j.1440-1711.2006.01451.x.

DOI:10.1111/j.1440-1711.2006.01451.x
PMID:16834574
Abstract

Rapid progression of hepatitis C virus (HCV) disease in patients with HIV/HCV may reflect different cytokine responses and be influenced by HCV genotype. This is addressed by a study of patients with HIV/HCV coinfection and infection with HCV genotype 2 or 3 (2/3). They are compared with coinfected patients infected with genotype 1 and HCV monoinfected patients matched for HCV genotype. IFN-gamma, IL-10, IL-4 and IL-4delta2 mRNA were quantified by real-time PCR in unstimulated PBMC and after in vitro stimulation with HCV core or nonstructural 3/4A antigen. In unstimulated PBMC, levels of IFN-gamma and IL-4 mRNA were lowest in HIV/HCV genotype 1 patients, intermediate in HIV/HCV genotype 2/3 patients and highest in HCV genotype 2/3 patients. Neither HCV genotype nor HIV affected levels of IL-10 mRNA in unstimulated PBMC or IFN-gamma, IL-4 and IL-10 mRNA in PBMC stimulated with HCV antigens. Levels of IL-4 and IL-4delta2 mRNA correlated in mitogen-stimulated PBMC from all patient groups but both were low in HIV/HCV genotype 1 patients. Serum soluble CD30 levels (a putative marker of a T2 cytokine environment) did not differ between patient groups. The data do not suggest a shift in the T1/T2 balance driven by HIV coinfection or HCV genotype but either may affect IL-4 bioavailability.

摘要

人类免疫缺陷病毒(HIV)/丙型肝炎病毒(HCV)合并感染患者中丙型肝炎病毒(HCV)疾病的快速进展可能反映出不同的细胞因子反应,并受HCV基因型影响。一项针对HIV/HCV合并感染以及感染HCV基因2型或3型(2/3型)患者的研究探讨了这一问题。将他们与感染基因1型的合并感染患者以及按HCV基因型匹配的HCV单一感染患者进行比较。通过实时聚合酶链反应(PCR)对未受刺激的外周血单个核细胞(PBMC)以及经HCV核心抗原或非结构蛋白3/4A抗原体外刺激后的PBMC中的γ干扰素(IFN-γ)、白细胞介素10(IL-10)、白细胞介素4(IL-4)和IL-4δ2信使核糖核酸(mRNA)进行定量分析。在未受刺激的PBMC中,HIV/HCV基因1型患者的IFN-γ和IL-4 mRNA水平最低,HIV/HCV基因2/3型患者的水平处于中间,而HCV基因2/3型患者的水平最高。HCV基因型和HIV均未影响未受刺激的PBMC中IL-10 mRNA的水平,也未影响经HCV抗原刺激后的PBMC中IFN-γ、IL-4和IL-10 mRNA的水平。在所有患者组经丝裂原刺激的PBMC中,IL-4和IL-4δ2 mRNA水平呈正相关,但在HIV/HCV基因1型患者中两者均较低。各患者组之间血清可溶性CD30水平(T2细胞因子环境的一种假定标志物)并无差异。数据并不表明由HIV合并感染或HCV基因型驱动的T1/T2平衡发生改变,但两者均可能影响IL-4的生物利用度。

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