The meaning of tissue and serum HCV RNA quantitation in hepatitis C recurrence after liver transplantation: A retrospective study

被引:6
|
作者
Vasuri, Francesco [1 ]
Morelli, Maria Cristina [2 ]
Gruppioni, Elisa [1 ]
Fiorentino, Michelangelo [1 ]
Ercolani, Giorgio [2 ]
Cescon, Matteo [2 ]
Pinna, Antonio Daniele [2 ]
Grigioni, Walter Franco [1 ]
D'Errico-Grigioni, Antonia [1 ]
机构
[1] Univ Bologna, Pathol Unit, F Addarii Inst Oncol & Transplantat Pathol, S Orsola Malpighi Hosp, I-40138 Bologna, Italy
[2] Univ Bologna, Dept Surg & Transplantat, S Orsola Malpighi Hosp, I-40138 Bologna, Italy
关键词
Hepatitis C virus; HCV recurrence; OLT; Polymerase chain reaction; FIBROSIS PROGRESSION; VIRUS RECURRENCE; NATURAL-HISTORY; RECIPIENTS; REINFECTION; INFECTION; CORRELATE; BIOPSY; DONOR;
D O I
10.1016/j.dld.2012.11.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: While the role of serum HCV RNA quantitation in hepatitis C virus recurrence after liver transplantation is well established, the meaning of HCV RNA tissue quantitation is largely unclear, and no correlations with recipient outcome have been investigated yet. Aims: To assess the predictive value, and a possible prognostic role, of tissue and serum HCV RNA in first post-transplant biopsies. Methods: We retrospectively reviewed the first post-transplant biopsies of 83 recipients. Tissue and serum HCV RNA was quantitated by RT-PCR, and compared with serum, clinical and histological data. Results: HCV RNA quantitation allowed us to categorise recipients into three different risk groups: (1) tissue HCV RNA <= 1.5IU/ng with any serum HCV RNA; (2) tissue HCV RNA > 1.5IU/ng and serum HCV RNA < 40 x 10(6) copies/mL; (3) tissue HCV RNA > 1.5IU/ng and serum HCV RNA >= 40 x 10(6) copies/mL. Hepatitis C virus recurrence rates in the three groups were 68%, 91% and 100% (P = 0.004); hepatitis C virus-related mortality was 0%, 14% and 45% respectively (P < 0.001). Conclusions: This preliminary study on serum and tissue HCV RNA quantitation allows recipient "stratification" in prognostic groups, which could be applicable in the future for timely antiviral treatment and/or immunosuppression modulation. (c) 2012 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:505 / 509
页数:5
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