Abstract | BACKGROUND: We report a case of acute rejection of a liver graft, together with the occurrence of de novo donor-specific antibodies (DSAs), in a 53-year-old Japanese man who had undergone deceased-donor liver transplantation. METHODS: RESULTS: DSA was absent 6 months after transplantation. HCV recurrence was treated with pegylated interferon-α-2a. Renal function deteriorated with this anti-HCV therapy, with serum cyclosporine levels decreasing to 50 ng/mL. A rapid virologic response was achieved, but liver function deteriorated after 3 months of anti-HCV therapy, with histologic evidence of acute cellular rejection and formation of de novo DSAs. Anti-thymocyte globulin was administered for 5 days, which led to immediate improvement in liver function. However, renal function declined, warranting hemodialysis. The patient recovered 2 months after acute rejection, although de novo DSAs persisted. CONCLUSIONS:
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Authors | R Nakano, M Ohira, K Ishiyama, K Ide, T Kobayashi, H Tahara, S Shimizu, K Arihiro, M Imamura, K Chayama, Y Tanaka, H Ohdan |
Journal | Transplantation proceedings
(Transplant Proc)
Vol. 49
Issue 7
Pg. 1634-1638
(Sep 2017)
ISSN: 1873-2623 [Electronic] United States |
PMID | 28838454
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright © 2017 Elsevier Inc. All rights reserved. |
Chemical References |
- Antibodies
- Antilymphocyte Serum
- Antiviral Agents
- Cyclosporins
- Immunosuppressive Agents
- Interferon-alpha
- Recombinant Proteins
- Polyethylene Glycols
- peginterferon alfa-2a
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Topics |
- Antibodies
(immunology)
- Antibody Specificity
- Antilymphocyte Serum
(therapeutic use)
- Antiviral Agents
(adverse effects)
- Cyclosporins
(blood)
- Graft Rejection
(blood, chemically induced, immunology)
- Hepacivirus
(immunology)
- Hepatitis C, Chronic
(drug therapy, virology)
- Humans
- Immunosuppressive Agents
(blood)
- Interferon-alpha
(adverse effects)
- Liver Transplantation
(adverse effects)
- Male
- Middle Aged
- Monitoring, Immunologic
- Plasmapheresis
- Polyethylene Glycols
(adverse effects)
- Postoperative Complications
(drug therapy, virology)
- Recombinant Proteins
(adverse effects)
- Recurrence
- Tissue Donors
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