Chronic rejection (CR) of liver allografts causes damage to intrahepatic vessels and bile ducts and may lead to graft failure after liver transplantation. Although its prevalence has declined steadily with the introduction of potent immunosuppressive therapy, CR still represents an important cause of graft injury, which might be irreversible, leading to graft loss requiring re-transplantation. To date, we still do not fully appreciate the mechanisms underlying this process. In addition to T cell-mediated CR, which was initially the only recognized type of CR, recently a new form of liver allograft CR, antibody-mediated CR, has been identified. This has indeed opened an era of thriving research and renewed interest in the field. Liver biopsy is needed for a definitive diagnosis of CR, but current research is aiming to identify new non-invasive tools for predicting patients at risk for CR after liver transplantation. Moreover, the minimization or withdrawal of immunosuppressive therapy might influence the establishment of subclinical CR-related injury, which should not be disregarded. Therapies for CR may only be effective in the "early " phases, and a tailored management of the immunosuppression regimen is essential for preventing irreversible liver damage. Herein, we provide an overview of the current knowledge and research on CR, focusing on early detection, identification of non-invasive biomarkers, immunosuppressive management, re-transplantation and future perspectives of CR.

Angelico, R., Sensi, B., Manzia, T.m., Tisone, G., Grassi, G., Signorello, A., et al. (2021). Chronic rejection after liver transplantation: Opening the Pandora's box. WORLD JOURNAL OF GASTROENTEROLOGY, 27(45), 7771-7783 [10.3748/wjg.v27.i45.7771].

Chronic rejection after liver transplantation: Opening the Pandora's box

Angelico, Roberta;Manzia, Tommaso M;Tisone, Giuseppe;Milana, Martina;Lenci, Ilaria;Baiocchi, Leonardo
2021-12-07

Abstract

Chronic rejection (CR) of liver allografts causes damage to intrahepatic vessels and bile ducts and may lead to graft failure after liver transplantation. Although its prevalence has declined steadily with the introduction of potent immunosuppressive therapy, CR still represents an important cause of graft injury, which might be irreversible, leading to graft loss requiring re-transplantation. To date, we still do not fully appreciate the mechanisms underlying this process. In addition to T cell-mediated CR, which was initially the only recognized type of CR, recently a new form of liver allograft CR, antibody-mediated CR, has been identified. This has indeed opened an era of thriving research and renewed interest in the field. Liver biopsy is needed for a definitive diagnosis of CR, but current research is aiming to identify new non-invasive tools for predicting patients at risk for CR after liver transplantation. Moreover, the minimization or withdrawal of immunosuppressive therapy might influence the establishment of subclinical CR-related injury, which should not be disregarded. Therapies for CR may only be effective in the "early " phases, and a tailored management of the immunosuppression regimen is essential for preventing irreversible liver damage. Herein, we provide an overview of the current knowledge and research on CR, focusing on early detection, identification of non-invasive biomarkers, immunosuppressive management, re-transplantation and future perspectives of CR.
7-dic-2021
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/12 - GASTROENTEROLOGIA
English
Antibody-mediated rejection
Chronic rejection
Complications
Donor-specific antibody
Graft loss
Immunosuppression
Liver transplantation
Outcomes
Re-transplantation
T cell-mediated rejection
Bile Ducts
Graft Rejection
Humans
Immunosuppression Therapy
Immunosuppressive Agents
Liver Transplantation
Angelico, R., Sensi, B., Manzia, T.m., Tisone, G., Grassi, G., Signorello, A., et al. (2021). Chronic rejection after liver transplantation: Opening the Pandora's box. WORLD JOURNAL OF GASTROENTEROLOGY, 27(45), 7771-7783 [10.3748/wjg.v27.i45.7771].
Angelico, R; Sensi, B; Manzia, Tm; Tisone, G; Grassi, G; Signorello, A; Milana, M; Lenci, I; Baiocchi, L
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/284541
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