Jawed Rohil
Department of Biomedical Engineering, College of Engineering and Applied Sciences, Nanjing University, Nanjing, 210023, China.
State Key Laboratory of Developmental Genes and Human Disease, School of Life Science and Technology, Southeast University, Nanjing, Jiangsu, 210096, China.
Mol Biol Rep. 2025 Jun 14;52(1):593. doi: 10.1007/s11033-025-10646-5.
To evaluate the prevalence and clinical significance of autoantibodies to mitochondrial sulphite oxidase (SUOX) and glycogen phosphorylase (PYGL) in Chinese PBC patients.
Enzyme-linked immunosorbent assays (ELISA) were developed with purified SUOX and PYGL proteins. Serum samples from 780 PBC patients and 352 healthy controls were used for antibody detection. Statistical analysis was performed with antibody results and biochemical data from PBC patients.
Antibodies to SUOX and PYGL were found in 14.23% and 22.94% of PBC patients, but also in 6.53% and 9.37% of healthy controls. There is a significant positive correlation between anti-SUOX and -PYGL with anti-M2, -sp100 and -gp210. Anti-SUOX and -PYGL positivity does not correlate with ursodeoxycholic acid (UDCA) response. Time course analysis found no specific change of anti-SUOX or -PYGL antibody titers in positive patients before and after UDCA treatment.
The data concluded that anti-SUOX and -PYGL autoantibodies are not serological markers in PBC diagnosis due to a lack of sensitivity and specificity. With the existence of PBC specific autoantibodies in PBC diagnosis and treatment, anti-SUOX and -PYGL status in PBC patients have no significant value.
评估中国原发性胆汁性胆管炎(PBC)患者中线粒体亚硫酸盐氧化酶(SUOX)和糖原磷酸化酶(PYGL)自身抗体的患病率及其临床意义。
用纯化的SUOX和PYGL蛋白建立酶联免疫吸附测定(ELISA)法。采用780例PBC患者和352例健康对照者的血清样本进行抗体检测。对PBC患者的抗体检测结果和生化数据进行统计学分析。
在14.23%的PBC患者中检测到抗SUOX抗体,在22.94%的PBC患者中检测到抗PYGL抗体;在6.53%的健康对照者中检测到抗SUOX抗体,在9.37%的健康对照者中检测到抗PYGL抗体。抗SUOX和抗PYGL与抗M2、抗sp100和抗gp210之间存在显著正相关。抗SUOX和抗PYGL阳性与熊去氧胆酸(UDCA)反应无关。时间进程分析发现,UDCA治疗前后,阳性患者的抗SUOX或抗PYGL抗体滴度无特异性变化。
数据表明,由于缺乏敏感性和特异性,抗SUOX和抗PYGL自身抗体不是PBC诊断的血清学标志物。鉴于PBC诊断和治疗中存在PBC特异性自身抗体,PBC患者的抗SUOX和抗PYGL状态无显著价值。