Bi Hui-Juan, Wang Jian, Huang He-Sheng, Liu Jun-Hua
Department of Aetiology and Immunology, Medicine College, Anhui University of Science and Technology, Huainan 232001, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2012 Apr;28(4):422-5.
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.
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.
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);).
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.
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。
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。
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)。
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。