Abstract | BACKGROUND: The use of hepatitis B core antibody (HBcAb+) and hepatitis C antibody (HCV Ab+) positive donors represents one strategy to increase available donor organs, but this remains controversial because of concern for viral transmission to recipients. We hypothesized that isolated HBcAb+ donors represent minimal risk of viral transmission in vaccinated lung transplant (LTx) recipients. METHODS: RESULTS: Between April 1992 and August 2003, 456 LTx operations were performed. Twenty-nine patients (HB group) received HBcAb+ allograft transplants with a median posttransplant follow-up of 24.5 months. Three critically ill patients (HC group) received HCV Ab+ allografts with a median follow-up of 21.5 months. One-year survival for the HB group is 83% versus 82% for all patients who received non-HB organs (P=0.36). No patient in the HB group developed clinical liver disease because of viral hepatitis, and all patients alive (n=21) at follow-up are, to date, HBV DNA and/or HBcAb negative. All patients in the HC group tested HCV RNA positive; one patient died of liver failure at 22 months. CONCLUSIONS: Risk of viral transmission with HCV Ab+ allografts seems high after LTx. However, the use of HBcAb+ pulmonary allografts in recipients with prior hepatitis B vaccination seems to be a safe and effective strategy to increase organ availability.
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Authors | Matthew G Hartwig, Vijay Patel, Scott M Palmer, Edward Cantu, James Z Appel, Robert H Messier, R Duane Davis |
Journal | Transplantation
(Transplantation)
Vol. 80
Issue 3
Pg. 320-5
(Aug 15 2005)
ISSN: 0041-1337 [Print] United States |
PMID | 16082326
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Hepatitis B Antibodies
- Hepatitis B Core Antigens
- Immunosuppressive Agents
- RNA, Viral
- DNA
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Topics |
- Adult
- Bronchiolitis Obliterans
(etiology, therapy)
- Cadaver
- DNA
(metabolism)
- Female
- Follow-Up Studies
- Graft Rejection
- Hepacivirus
(genetics)
- Hepatitis B
(immunology)
- Hepatitis B Antibodies
(metabolism)
- Hepatitis B Core Antigens
(immunology, metabolism)
- Hepatitis B virus
(genetics)
- Humans
- Immunosuppressive Agents
(therapeutic use)
- Liver
(metabolism)
- Lung Transplantation
(methods)
- Male
- Middle Aged
- Polymerase Chain Reaction
- RNA, Viral
(metabolism)
- Retrospective Studies
- Time Factors
- Tissue Donors
- Tissue and Organ Procurement
(methods)
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