实用肝脏病杂志 ›› 2023, Vol. 26 ›› Issue (6): 855-858.doi: 10.3969/j.issn.1672-5069.2023.06.022

• 肝硬化 • 上一篇    下一篇

慢性乙型肝炎和乙型肝炎肝硬化患者PBMCs 信号转导和转录激活因子3及血清可溶性CD30分子水平变化及其临床意义探讨*

邹涛, 张敏, 杨凡, 王丽, 喻峰   

  1. 433000 湖北省仙桃市 长江大学附属仙桃市第一人民医院输血科(邹涛);心内科(张敏);儿科(杨凡);医学检验科(王丽);静配中心(喻峰)
  • 收稿日期:2023-01-10 出版日期:2023-11-10 发布日期:2023-11-20
  • 通讯作者: 杨凡,E-mail:2738253884@qq.com
  • 作者简介:邹涛,男,44岁,大学本科,主管技师。E-mail:fkbg0112@163.com
  • 基金资助:
    * 湖北省卫健委科研项目(编号:WJ2017F127)

Implication of peripheral blood mononuclear cell signal transducer and activator of transcription 3 and serum soluble CD30 levels in patients with chronic hepatitis B and hepatitis B cirrhosis

Zou Tao, Zhang Min, Yang Fan, et al   

  1. Department of Blood Transfusion, First People's Hospital Affiliated to Changjiang University, Xiantao 433000, Hubei Province, China
  • Received:2023-01-10 Online:2023-11-10 Published:2023-11-20

摘要: 目的 探讨慢性乙型肝炎(CHB)和乙型肝炎肝硬化患者外周血单个核细胞(PBMC)信号转导和转录激活因子3(STAT3)和血清可溶性CD30分子(sCD30)水平变化及其临床意义。方法 2019年12月~2021年12月我院诊治的CHB患者45例(HBeAg阳性25例,HBeAg阴性20例)和乙型肝炎肝硬化患者38例(代偿期22例,失代偿期16例),另选择健康人40例,分离PBMC,采用RT-PCR法检测STAT3 mRNA,采用ELISA法检测血清sCD30水平。给予两组患者抗病毒和护肝治疗。结果 肝硬化组PBMC STAT3 mRNA和血清sCD30水平分别为(1.6±0.4)和(60.3±12.9)U/L,均显著高于CHB组【分别为(1.3±0.3)和(51.8±10.2)U/L,P<0.05】或健康人【分别为(0.5±0.1)和(10.6±2.4)U/L,P<0.05】;25例血清HBeAg阳性患者STAT3 mRNA和sCD30水平分别为(1.4±0.3)和(57.2±11.9)U/L,均显著高于20例HBeAg阴性患者【分别为(1.2±0.3)和(45.1±8.1),P<0.05】,16例失代偿期肝硬化患者STAT3 mRNA和sCD30水平分别为(1.8±0.5)和(70.5±14.3)U/L,均显著高于22例代偿期肝硬化患者【分别为(1.4±0.3)和(52.9±11.8),P<0.05】;经抗病毒或/和护肝治疗3个月和6个月,CHB患者STAT3 mRNA和sCD30水平呈进行性降低,其中肝硬化患者STAT3 mRNA和sCD30水平分别为(1.2±0.2)和(43.6±8.3)U/L及(0.7±0.2)和(21.5±3.7)U/L,显著低于治疗前(P<0.05)。结论 CHB和乙型肝炎肝硬化患者PBMC STAT3和血清sCD30水平升高,与病情进展关系密切,值得临床进行监测和深入研究。

关键词: 肝硬化, 慢性乙型肝炎, 信号转导和转录激活因子3, 可溶性CD30, 临床意义

Abstract: Objective The purpose of this study was to investigate the implication of peripheral blood mononuclear cell (PBMCs) signal transducer and activator of transcription 3 (STAT3) and serum soluble CD30 (sCD30) levels in patients with chronic hepatitis B (CHB) and hepatitis B cirrhosis. Methods 45 patients with CHB and 38 patients with hepatitis B cirrhosis were encountered in our hospital between December 2019 and December 2021, and 40 healthy volunteers matched by gender and age were selected as control. The PBMCs were separated and the STAT3 mRNA was assayed by RT-PCR. Serum SCD30 level was detected by ELISA. All patients with CHB and hepatitis B cirrhosis received antiviral therapy, and the cirrhotics were also managed by liver-protecting medicines. Results The PBMC STAT3 mRNA load and serum sCD30 level in patients with liver cirrhosis were (1.6±0.4) and (60.3±12.9)U/L, both significantly higher than [(1.3±0.3) and (51.8±10.2)U/L, P<0.05] in patients with CHB or [(0.5±0.1) and (10.6±2.4)U/L, respectively, P<0.05] in healthy volunteers; the STAT3 mRNA and sCD30 level in 25 CHB patients with serum HBeAg positive were (1.4±0.3) and (57.2±11.9)U/L, both significantly higher than [(1.2±0.3) and (45.1±8.1), respectively P<0.05] in 20 CHB patients with serum HBeAg negative, and the STAT3 mRNA and sCD30 level in 16 patients with decompensated cirrhosis were (1.8±0.5) and (70.5±14.3)U/L, both significantly higher than [(1.4±0.3) and (52.9±11.8), respectively, P<0.05] in 22 patients with compensated cirrhosis; at the end of three-month and six-month treatment, the STAT3 mRNA and sCD30 level in patients with CHB and with hepatitis B cirrhosis decreased gradually, out of which, the STAT3 mRNA and sCD30 levels in patients with cirrhosis were (1.2±0.2) and (43.6±8.3)U/L, and (0.7±0.2) and (21.5±3.7)U/L, all significantly lower than at inclusion (P<0.05). Conclusion The PBMC STAT3 and serum sCD30 levels in patients with CHB and hepatitis B cirrhosis are up-regulated, which might be related to the deterioration of the disease, and needs further investigation.

Key words: Liver Cirrhosis, Hepatitis B, Signal transducer and activator of transcription 3, Soluble CD30, Clinical implication