Role of immunohistochemistry for hepatitis D and hepatitis B virus in hepatitis delta

被引:5
|
作者
Kabacam, Gokhan [1 ]
Wedemeyer, Heiner [2 ]
Savas, Berna [3 ]
Keskin, Onur [1 ]
Dalekos, George [4 ,5 ]
Tabak, Fehmi [6 ]
Idilman, Ramazan [1 ]
Erhardt, Andreas [7 ]
Yalcin, Kendal [8 ]
Bozdayi, Mithat A. [1 ]
Bozkaya, Hakan [1 ]
Manns, Michael [2 ]
Dienes, Hans [9 ]
Yurdaydin, Cihan [1 ]
机构
[1] Ankara Univ, Dept Gastroenterol, Sch Med, TR-06100 Ankara, Turkey
[2] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, Hannover, Germany
[3] Ankara Univ, Dept Pathol, Sch Med, TR-06100 Ankara, Turkey
[4] Univ Thessaly, Sch Med, Dept Internal Med, Acad Liver Unit, Larisa, Greece
[5] Univ Thessaly, Sch Med, Res Lab Internal Med, Larisa, Greece
[6] Istanbul Univ, Cerrahpasa Med Sch, Dept Infect Dis, Istanbul, Turkey
[7] Univ Dusseldorf, Dept Gastroenterol Hepatol & Infect Dis, Dusseldorf, Germany
[8] Dicle Univ, Fac Med, Dept Gastroenterol, Diyarbakir, Turkey
[9] Univ Cologne, Inst Pathol, Cologne, Germany
关键词
Chronic Delta Hepatitis; Delta Antigen; HBcAg; HBsAg; Immunohistochemistry; Quantitative Surface Antigen; INTRAHEPATIC EXPRESSION; SURFACE-ANTIGEN; CORE ANTIGEN; LIVER; DISEASE; MARKERS; NUCLEAR; SERUM;
D O I
10.1111/liv.12376
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Immunohistochemical assessment of liver tissue in chronic delta hepatitis (CDH) is underinvestigated. Aim of the study was (i) to assess variables associated with hepatitis D antigen (HDAg), hepatitis B surface antigen (HBsAg) and hepatitis B core antigen (HBcAg) staining in the liver. Methods: Demographic, biochemical and virologic data collected from the HIDIT 1 study were used. HBsAg, HBcAg and HDAg immunohistochemical (IHC) staining was semiquantitatively assessed. Results: Hepatitis D antigen immunohistochemical staining displayed positive correlations with age and alanine aminotransferase (ALT) and negative correlations with serum HBsAg (P = 0.01 for all). HBsAg IHC displayed a negative correlation with gamma glutamyl transferase and positive correlations with serum HBV DNA, serum HBsAg levels and HBeAg serology (P < 0.001, P = 0.02 and P = 0.007 respectively). HBcAg staining was mainly nuclear and displayed negative correlations with serum HBsAg and histologic activity (P = 0.002 and P = 0.02 respectively). Pegylated IFN based treatment led to a decline of all IHC markers, however, these markers had no impact on treatment outcome. Conclusions: These data suggest an association of liver injury with HDAg expression in CDH whereas the negative correlation between HBcAg expression and liver injury and the overall nuclear localization of HBcAg suggest that HBcAg does not contribute to liver injury in CDH. HDV cases with high level of HBV replication, high serum HBsAg levels, HBeAg positivity, that are probably in the earlier stages of disease (low gamma-glutamyl transferase), had a more intense HBsAg staining profile. Overall, the data enforce the importance of HDAg and HBsAg in different phases of CDH infection.
引用
收藏
页码:1207 / 1215
页数:9
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