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[干扰素对慢性乙型肝炎患者趋化因子受体CXCR1、CXCR2及其配体IL-8表达的影响]

[Influence of IFN on expression of chemokine receptor CXCR1, CXCR2 and their ligand IL-8 in the patients with chronic hepatitis B].

作者信息

Bi Hui-Juan, Wang Jian, Huang He-Sheng, Liu Jun-Hua

机构信息

Department of Aetiology and Immunology, Medicine College, Anhui University of Science and Technology, Huainan 232001, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2012 Apr;28(4):422-5.

Abstract

AIM

To study the mRNA levels of chemokine receptor CXCR1, CXCR2 and IL-8 in the patients with chronic hepatitis B and their association with IFN therapy.

METHODS

The mRNA levels of CXCR1, CXCR2 and IL-8 in peripheral blood mononuclear cells(PBMC)of chronic hepatitis B patients were determined by real-time RT-PCR before and during the IFN-α therapy.

RESULTS

The mRNA levels of CXCR1(0.4474 ± 0.0386)and IL-8(1.1897 ± 0.1028)in peripheral blood of the patients with chronic hepatitis B were significantly higher than those in healthy donors(P<0.01). The mRNA level of CXCR2(0.4720 ± 0.0458)was higher than those in healthy donors, but there was no significant differences between the two groups. During the treatment, the mRNA levels of CXCR1, CXCR2 and IL-8 obviously decreased. After treatment for six month, the mRNA level of CXCR1(0.4129 ± 0.0395), CXCR2(0.4461 ± 0.0477) and IL-8(0.8660 ± 0.1307)were significantly lower than those before treatment(P<0.01 or P<0.05). Additionally, the expressive levels of CXCR1, CXCR2 and IL-8 in the high HBV loading group(HBV-DNA>10(6);)were much higher than those in the low HBV loading group(HBV-DNA<10(6);).

CONCLUSION

CXCR1 and IL-8 may contribute to hepatic inflammation. Among them, CXCR1, CXCR2 and IL-8 decrease after IFN treatment, which illustrates that IFN-α plays an important role in down-regulating inflammation response, controlling the development of the patients' condition.

摘要

目的

研究慢性乙型肝炎患者趋化因子受体CXCR1、CXCR2及白细胞介素-8(IL-8)的mRNA水平及其与干扰素治疗的相关性。

方法

采用实时逆转录聚合酶链反应(RT-PCR)法检测慢性乙型肝炎患者外周血单个核细胞(PBMC)中CXCR1、CXCR2及IL-8的mRNA水平,检测时间为干扰素-α治疗前及治疗期间。

结果

慢性乙型肝炎患者外周血中CXCR1(0.4474±0.0386)及IL-8(1.1897±0.1028)的mRNA水平显著高于健康献血者(P<0.01)。CXCR2(0.4720±0.0458)的mRNA水平高于健康献血者,但两组间差异无统计学意义。治疗期间,CXCR1、CXCR2及IL-8的mRNA水平明显下降。治疗6个月后,CXCR1(0.4129±0.0395)、CXCR2(0.4461±0.0477)及IL-8(0.8660±0.1307)的mRNA水平显著低于治疗前(P<0.01或P<0.05)。此外,高乙肝病毒载量组(HBV-DNA>10⁶)中CXCR1、CXCR2及IL-8的表达水平远高于低乙肝病毒载量组(HBV-DNA<10⁶)。

结论

CXCR1和IL-8可能与肝脏炎症有关。其中,干扰素治疗后CXCR1、CXCR2及IL-8下降,说明干扰素-α在下调炎症反应、控制病情发展中起重要作用。

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