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De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody
PURPOSE: The use of hepatitis B core antibody (HBcAb)-positive grafts is increasing, especially where hepatitis B is endemic. However, this remains controversial because of the risk of development of de novo HBV infection. METHODS: We collected information obtained between January 2000 and December...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Surgical Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559617/ https://www.ncbi.nlm.nih.gov/pubmed/26366384 http://dx.doi.org/10.4174/astr.2015.89.3.145 |
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author | Han, Jae Hyun Kim, Dong Goo Na, Gun Hyung Kim, Eun Young Lee, Soo Ho Hong, Tae Ho You, Young Kyoung Choi, Jong Young Yoon, Seung Kew |
author_facet | Han, Jae Hyun Kim, Dong Goo Na, Gun Hyung Kim, Eun Young Lee, Soo Ho Hong, Tae Ho You, Young Kyoung Choi, Jong Young Yoon, Seung Kew |
author_sort | Han, Jae Hyun |
collection | PubMed |
description | PURPOSE: The use of hepatitis B core antibody (HBcAb)-positive grafts is increasing, especially where hepatitis B is endemic. However, this remains controversial because of the risk of development of de novo HBV infection. METHODS: We collected information obtained between January 2000 and December 2012 and retrospectively analyzed data on 187 HBsAg-negative donors and recipients were analyzed retrospectively. De novo HBV infection was defined as development of HBsAg positivity with or without detection of HBV DNA. RESULTS: Forty patients (21.4%) received HBcAb-positive grafts. Survival rate did not differ by donor HBcAb status (P = 0.466). De novo HBV infection occurred in five patients (12.5%) who were not treated with anti-HBV prophylaxis, and was significantly more prevalent in hepatitis B surface antibody (HBsAb)- and HBcAb-negative than HBsAb- and HBcAb-positive recipients (50% vs. 4.2%, P = 0.049). All patients except one were treated with entecavir with/without antihepatitis B immunoglobulin and four were negative in terms of HBV DNA seroconversion. No patient died. CONCLUSION: HBcAb-positive grafts are safe without survival difference. However, the risk of de novo hepatitis B virus infection was significantly increased in HBsAb- and HBcAb-negative recipients. All patients were successfully treated even after recurrence. |
format | Online Article Text |
id | pubmed-4559617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Korean Surgical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45596172015-09-11 De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody Han, Jae Hyun Kim, Dong Goo Na, Gun Hyung Kim, Eun Young Lee, Soo Ho Hong, Tae Ho You, Young Kyoung Choi, Jong Young Yoon, Seung Kew Ann Surg Treat Res Original Article PURPOSE: The use of hepatitis B core antibody (HBcAb)-positive grafts is increasing, especially where hepatitis B is endemic. However, this remains controversial because of the risk of development of de novo HBV infection. METHODS: We collected information obtained between January 2000 and December 2012 and retrospectively analyzed data on 187 HBsAg-negative donors and recipients were analyzed retrospectively. De novo HBV infection was defined as development of HBsAg positivity with or without detection of HBV DNA. RESULTS: Forty patients (21.4%) received HBcAb-positive grafts. Survival rate did not differ by donor HBcAb status (P = 0.466). De novo HBV infection occurred in five patients (12.5%) who were not treated with anti-HBV prophylaxis, and was significantly more prevalent in hepatitis B surface antibody (HBsAb)- and HBcAb-negative than HBsAb- and HBcAb-positive recipients (50% vs. 4.2%, P = 0.049). All patients except one were treated with entecavir with/without antihepatitis B immunoglobulin and four were negative in terms of HBV DNA seroconversion. No patient died. CONCLUSION: HBcAb-positive grafts are safe without survival difference. However, the risk of de novo hepatitis B virus infection was significantly increased in HBsAb- and HBcAb-negative recipients. All patients were successfully treated even after recurrence. The Korean Surgical Society 2015-09 2015-08-24 /pmc/articles/PMC4559617/ /pubmed/26366384 http://dx.doi.org/10.4174/astr.2015.89.3.145 Text en Copyright © 2015, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/4.0/ Annals of Surgical Treatment and Research is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Han, Jae Hyun Kim, Dong Goo Na, Gun Hyung Kim, Eun Young Lee, Soo Ho Hong, Tae Ho You, Young Kyoung Choi, Jong Young Yoon, Seung Kew De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody |
title | De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody |
title_full | De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody |
title_fullStr | De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody |
title_full_unstemmed | De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody |
title_short | De novo hepatitis B virus infection developing after liver transplantation using a graft positive for hepatitis B core antibody |
title_sort | de novo hepatitis b virus infection developing after liver transplantation using a graft positive for hepatitis b core antibody |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559617/ https://www.ncbi.nlm.nih.gov/pubmed/26366384 http://dx.doi.org/10.4174/astr.2015.89.3.145 |
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