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HIV infection induces age-related changes to monocytes and innate immune activation in young men that persist despite combination antiretroviral therapy.HIV 感染可诱导年轻男性单核细胞的衰老相关变化和固有免疫激活,尽管联合抗逆转录病毒治疗仍持续存在。
AIDS. 2012 Apr 24;26(7):843-53. doi: 10.1097/QAD.0b013e328351f756.
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Host response to translocated microbial products predicts outcomes of patients with HBV or HCV infection.宿主对移位微生物产物的反应可预测 HBV 或 HCV 感染患者的结局。
Gastroenterology. 2011 Oct;141(4):1220-30, 1230.e1-3. doi: 10.1053/j.gastro.2011.06.063. Epub 2011 Jul 2.
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Higher levels of CRP, D-dimer, IL-6, and hyaluronic acid before initiation of antiretroviral therapy (ART) are associated with increased risk of AIDS or death.在开始抗逆转录病毒治疗(ART)之前,CRP、D-二聚体、IL-6 和透明质酸水平较高与艾滋病或死亡风险增加相关。
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Plasma levels of soluble CD14 independently predict mortality in HIV infection.血浆可溶性 CD14 水平可独立预测 HIV 感染患者的死亡率。
J Infect Dis. 2011 Mar 15;203(6):780-90. doi: 10.1093/infdis/jiq118. Epub 2011 Jan 20.
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Development of fatal acute liver failure in HIV-HBV coinfected patients.HIV-HBV 合并感染患者发生致命性急性肝衰竭。
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Paucity of initial cerebrospinal fluid inflammation in cryptococcal meningitis is associated with subsequent immune reconstitution inflammatory syndrome.隐球菌性脑膜炎中初始脑脊液炎症的缺乏与随后的免疫重建炎症综合征有关。
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HBcAg induces interleukin-10 production, inhibiting HBcAg-specific Th17 responses in chronic hepatitis B patients.HBcAg 诱导白细胞介素-10 的产生,抑制慢性乙型肝炎患者 HBcAg 特异性 Th17 反应。
Immunol Cell Biol. 2010 Nov-Dec;88(8):834-41. doi: 10.1038/icb.2010.63. Epub 2010 May 25.
9
A longitudinal analysis of innate and adaptive immune profile during hepatic flares in chronic hepatitis B.慢性乙型肝炎肝发作期间固有和适应性免疫特征的纵向分析。
J Hepatol. 2010 Mar;52(3):330-9. doi: 10.1016/j.jhep.2009.12.015. Epub 2010 Jan 13.
10
Incidence and risk factors for chronic elevation of alanine aminotransferase levels in HIV-infected persons without hepatitis b or c virus co-infection.未合并乙型肝炎或丙型肝炎病毒感染的 HIV 感染者中丙氨酸氨基转移酶水平慢性升高的发生率和危险因素。
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炎症和凝血标志物与 HIV 和肝炎病毒合并感染人群的死亡率和肝炎发作有关。

Biomarkers of inflammation and coagulation are associated with mortality and hepatitis flares in persons coinfected with HIV and hepatitis viruses.

机构信息

Immunobiology Section, Laboratory of Parasitic Diseases, and.

出版信息

J Infect Dis. 2013 May 1;207(9):1379-88. doi: 10.1093/infdis/jit033. Epub 2013 Jan 18.

DOI:10.1093/infdis/jit033
PMID:23335804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3610421/
Abstract

BACKGROUND

Hepatitis C virus (HCV) and/or hepatitis B virus (HBV) coinfection with human immunodeficiency virus (HIV) has a greater risk of mortality than either HCV or HBV infection alone and is frequently associated with hepatitis flares after antiretroviral therapy (ART) initiation.

METHODS

We performed a retrospective cohort study of 287 HIV-positive persons coinfected with HBV and/or HCV (70 had HBV coinfection only, 207 had HCV coninfection only, and 10 had HBV and HCV coinfections) who had pre-ART plasma samples evaluated for biomarkers associated with death (within 4 years) and/or hepatitis flare (within 4 months) after ART initiation. A predictive biomarker risk score was calculated.

RESULTS

Forty-eight deaths and 50 hepatitis flares occurred. Nonsurvivors were older, had more prior AIDS-defining events, and had higher pre-ART triglycerides and aspartate transaminase levels. Detectable hyaluronic acid and higher d-dimer, interleukin 6, interleukin 8, and soluble CD14 levels were associated with death in univariate models and with a composite biomarker risk score. The risk of hepatitis flares was higher with HBV coinfection only (24.3%) and with HBV and HCV coinfection (50%) than with HCV coinfection only (13.5%). Higher levels of alanine transaminase and interleukin 10 were also associated with hepatitis flares.

CONCLUSIONS

Among HIV-positive patients coinfected with HBV and/or HCV who are initiating ART, biomarkers of inflammation and coagulation are associated with an increased risk of death, whereas HBV coinfection and higher pre-ART interleukin 10 levels are associated with hepatitis flares.

摘要

背景

丙型肝炎病毒(HCV)和/或乙型肝炎病毒(HBV)与人类免疫缺陷病毒(HIV)合并感染比单独感染 HCV 或 HBV 的死亡率更高,并且在抗逆转录病毒治疗(ART)启动后常伴有肝炎发作。

方法

我们对 287 例 HIV 阳性合并 HBV 和/或 HCV 感染的患者(70 例仅 HBV 合并感染,207 例仅 HCV 合并感染,10 例 HBV 和 HCV 合并感染)进行了回顾性队列研究,这些患者在 ART 启动前的血浆样本中评估了与死亡(4 年内)和/或肝炎发作(4 个月内)相关的生物标志物。计算了预测生物标志物风险评分。

结果

48 例死亡和 50 例肝炎发作。非幸存者年龄较大,有更多的艾滋病定义事件,并且在 ART 前的甘油三酯和天冬氨酸转氨酶水平较高。在单变量模型中,可检测的透明质酸和较高的 d-二聚体、白细胞介素 6、白细胞介素 8 和可溶性 CD14 水平与死亡相关,并与复合生物标志物风险评分相关。仅 HBV 合并感染(24.3%)和 HBV 和 HCV 合并感染(50%)的肝炎发作风险高于仅 HCV 合并感染(13.5%)。较高的丙氨酸转氨酶和白细胞介素 10 水平也与肝炎发作相关。

结论

在开始接受 ART 的 HIV 阳性合并 HBV 和/或 HCV 感染的患者中,炎症和凝血标志物与死亡风险增加相关,而 HBV 合并感染和较高的 ART 前白细胞介素 10 水平与肝炎发作相关。