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在进行乙肝病毒活性抗逆转录病毒治疗后,CXC趋化因子配体10、白细胞介素-12和白细胞介素-21并非HIV-1-HBV合并感染中HBeAg血清学转换的免疫预测指标。

CXCL-10, interleukin-12 and interleukin-21 are not immunological predictors of HBeAg seroconversion in HIV-1-HBV coinfection following HBV-active antiretroviral therapy.

作者信息

Giarda Paola, Avihingsanon Anchalee, Sasadeusz Joe, Audsley Jennifer, Marks Pip, Matthews Gail, Ruxrungtham Kiat, Lewin Sharon R, Crane Megan

机构信息

Department of Translational Medicine, Università degli Studi del Piemonte Orientale 'A Avogadro', Novara, Italy.

出版信息

Antivir Ther. 2014;19(4):429-33. doi: 10.3851/IMP2720. Epub 2014 Jan 16.

Abstract

BACKGROUND

Interferon stimulated chemokine CXCL-10, interleukin (IL)-12 (p70) and IL-21 have been associated with HBsAg and HBeAg loss following treatment of HBV monoinfection. The aim of this study was to determine whether these factors were also associated with HBsAg and HBeAg loss in HIV-HBV-coinfected patients following HBV-active combination antiretroviral therapy (cART).

METHODS

HIV-HBV-coinfected patients with HBeAg seroconversion (n=12; seroconverters [SC]) were compared to patients who did not seroconvert (n=13; non-seroconverters [NSC]). CXCL-10, IL-12 and IL-21 (Luminex Bead Array, Life Technologies, Grand Island, NY, USA) were measured in plasma prior to initiation of HBV-active cART (baseline), at the time of seroconversion (T0) and at the closest time point before (T-1) and after (T+1) seroconversion.

RESULTS

Levels of CXCL-10 declined significantly in all patients following HBV-active cART (P<0.05 for both SC and NSC; Kruskall-Wallis, Dunn's post-test). There was no difference between SC and NSC in the level of CXCL-10, IL-12 and IL-21 at any time point.

CONCLUSIONS

We found no evidence that CXCL-10, IL-12 or IL-21 were associated with HBeAg seroconversion following HBV-active cART. Other immunological determinants should be explored in this setting.

摘要

背景

干扰素刺激趋化因子CXCL - 10、白细胞介素(IL)- 12(p70)和IL - 21与单纯HBV感染治疗后的HBsAg和HBeAg消失有关。本研究的目的是确定这些因素在HIV - HBV合并感染患者接受HBV活性联合抗逆转录病毒治疗(cART)后是否也与HBsAg和HBeAg消失有关。

方法

将发生HBeAg血清学转换的HIV - HBV合并感染患者(n = 12;血清学转换者[SC])与未发生血清学转换的患者(n = 13;未血清学转换者[NSC])进行比较。在开始HBV活性cART之前(基线)、血清学转换时(T0)以及血清学转换前(T - 1)和后(T + 1)最接近的时间点,用血浆检测CXCL - 10、IL - 12和IL - 21(美国纽约州大岛市赛默飞世尔科技公司的Luminex微球阵列)。

结果

所有患者在接受HBV活性cART后,CXCL - 10水平均显著下降(SC和NSC均P<0.05;Kruskal - Wallis检验,Dunn事后检验)。在任何时间点,SC和NSC之间的CXCL - 10、IL - 12和IL - 21水平均无差异。

结论

我们没有发现证据表明CXCL - 10、IL - 12或IL - 21与HBV活性cART后的HBeAg血清学转换有关。在此情况下应探索其他免疫决定因素。

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