Selmi Carlo, Zuin Massimo, Bowlus Christopher L, Gershwin M Eric
Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis School of Medicine, 451 E. Health Sciences Drive, Suite 6510, Davis, CA 95616, USA.
Clin Liver Dis. 2008 Feb;12(1):173-85, ix. doi: 10.1016/j.cld.2007.11.008.
The recent development in the authors' laboratory of a sensitive bead assay able to detect AMA in 20% of otherwise AMA-negative sera seems to support the hypothesis that many AMA-negative cases of primary biliary cirrhosis (PCB) are secondary to limits in the methods used and do not represent an independent clinical entity. Clinical data demonstrate that patients without detectable serum AMA do not differ in their natural history from their seropositive counterparts. Anti-nuclear antibodies have been associated repeatedly with more severe disease and are helpful tools in the management of patients who have PBC, particularly those lacking AMA.
作者实验室最近开发出一种灵敏的珠粒检测法,能够在20%原本AMA阴性的血清中检测到AMA,这似乎支持了以下假说:许多原发性胆汁性肝硬化(PCB)的AMA阴性病例是由于所用方法的局限性所致,并非独立的临床实体。临床数据表明,血清AMA检测不到的患者与血清阳性的患者在自然病程上并无差异。抗核抗体反复与更严重的疾病相关,是管理原发性胆汁性肝硬化患者,尤其是那些缺乏AMA的患者的有用工具。