Evidence for the association between IgG-antimitochondrial antibody and biochemical response to ursodeoxycholic acid treatment in primary biliary cholangitis
Evidence for the association between IgG-antimitochondrial antibody and biochemical response to ursodeoxycholic acid treatment in primary biliary cholangitis
复制标题
IgG 抗线粒体抗体与熊去氧胆酸治疗原发性胆汁性胆管炎生化反应之间相关性的证据
DOI:
10.1111/jgh.13534
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发表时间:
2017
影响因子:
4.1
通讯作者:
Hou Jinlin
中科院分区:
文献类型:
--
作者:
Tang Libo;Zhong Ruihua;He Xuanqiu;Wang Weibin;Liu Jinhong;Zhu Youfu;Li Yongyin;Hou Jinlin
Background and AimAntimitochondrial antibody (AMA) is considered the serological hallmark of primary biliary cholangitis (PBC), while data regarding the profile of AMA during ursodeoxycholic acid (UDCA) treatment are scarce. Here, we assessed the influence of UDCA treatment on titers of AMA and factors relevant to its production.MethodsSerum IgA‐AMA, IgM‐AMA, IgG‐AMA, B cell‐activating factor of the tumor necrosis factor family (BAFF), and the frequency of circulating plasmablasts were detected in PBC patients, including those who received UDCA therapy for 24 weeks, healthy controls, chronic hepatitis B patients, and autoimmune hepatitis patients. Consecutive liver sections from controls and PBC patients were stained by immunohistochemistry for detection of intrahepatic CD38+, IgA+, IgM+, and IgG+cells.ResultsSignificant decrease in titers of IgG‐AMA was found only confined to PBC patients with biochemical response to UDCA treatment (P= 0.005), and similar pattern was also observed at week 24 in quantifying circulating plasmablasts (P= 0.025) and serum BAFF (P= 0.013). Notably, positive correlation between serum BAFF levels and titers of IgG‐AMA, and the frequency of circulating plasmablasts were observed in PBC patients (r= 0.464,P= 0.034 andr= 0.700,P< 0.001, respectively). Additionally,in situstaining revealed significant accumulation of CD38+and IgG+cells within the portal tracts of PBC liver.ConclusionsDecreased titers of serum IgG‐AMA are associated with biochemical response to UDCA treatment, implicating the potentiality of this hallmark in therapeutic response evaluation and the beneficial effect of UDCA on humoral immunity in PBC patients.