A novel assay for detecting antibodies to cytochrome P4502D6, the molecular target of liver kidney microsomal antibody type 1

被引:11
作者
Kerkar, N
Ma, Y
Hussain, M
Muratori, L
Targett, C
Williams, R
Bianchi, FB
Mieli-Vergani, G
Vergani, D
机构
[1] UCL, Sch Med, Inst Hepatol, Immunol Sect, London WC1E 6HX, England
[2] Kings Coll London, Sch Med & Dent, Dept Child Hlth, London SE5 9PJ, England
[3] Univ Bologna, Dept Internal Med Cardioangiol Hepatol, Bologna, Italy
[4] Kings Coll London, Sch Med & Dent, Dept Immunol, London SE5 9PJ, England
关键词
enzyme-linked immunosorbent assay; autoimmune hepatitis; hepatitis C virus infection;
D O I
10.1016/S0022-1759(98)00213-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Liver Kidney Microsomal type 1 (LKM1) antibody, the diagnostic marker of autoimmune hepatitis type 2, is also found in a proportion of patients with hepatitis C virus infection (HCV). It is detected conventionally by the subjective immunofluorescence technique. Our aim was to establish a simple and objective enzyme-linked immunosorbent assay (ELISA) that measures antibodies to cytochrome P4502D6 (CYP2D6), the target of LKM1. An indirect ELISA using eukaryotically expressed CYP2D6 was designed. Absorbance values obtained against a reference microsomal preparation were subtracted from those obtained against a microsomal preparation over-expressing CYP2D6, thus removing the non-CYP2D6-specific reaction. Sera from 51 LKM1 positive patients (21 autoimmune hepatitis and 30 with HCV infection), 111 LKM1 negative patients with chronic liver disease (including 20 with HCV infection) and 43 healthy controls were tested. Of 51 patients positive by immunofluorescence, 48 were also positive by ELISA while all the 154 LKM1 negative subjects were also negative by ELISA. There was a high degree of association between IFL and ELISA as demonstrated by a kappa reliability value of 0.96. The absorbance values by ELISA correlated with immunofluorescence LKM1 titres both in autoimmune hepatitis (r = 0.74, p < 0.001) and HCV infection (r = 0.67, p < 0.001). The simple, objective ELISA described has the potential to replace the standard immunofluorescence technique. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:227 / 235
页数:9
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