Immune benefit of combined heart and liver transplantation.


Journal

Current opinion in organ transplantation
ISSN: 1531-7013
Titre abrégé: Curr Opin Organ Transplant
Pays: United States
ID NLM: 9717388

Informations de publication

Date de publication:
10 2020
Historique:
pubmed: 4 9 2020
medline: 12 2 2021
entrez: 4 9 2020
Statut: ppublish

Résumé

Understanding the mechanisms involved in immune protection provided by a hepatic allograft is imperative as further therapies for highly sensitized patients could be developed and thus expanding the donor pool and improving outcomes. The clinical data from immune protection comes mainly from combined liver and kidney transplants with excellent results in overall survival and also that of the allograft. This phenomenon has also been observed in dual liver transplants with heart, lung, skin and intestines, albeit with less data. In heart transplant recipients, the liver allograft has proven to be protective even in cases of highly sensitized patients with at least equal survival and rejection outcomes to recipients of heart alone. Although not fully understood, the mechanisms for immune benefit proposed are extensive at different levels of the hepatic immune system. Some of these mechanisms include chimerism, T-cell deletion, the presence of peripheral regulatory T cells and donor-specific antibody neutralization. Combined heart and liver transplantation is an infrequent but growing procedure due to increasing need in the adult congenital heart disease and cardiac amyloid populations. Given the ever expanding need for heart transplantation, understanding immunological phenomena that could expand the donor pool could, subsequently, increase the number of transplants.

Identifiants

pubmed: 32881718
doi: 10.1097/MOT.0000000000000801
pii: 00075200-202010000-00012
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

513-518

Références

Zhao K, Mclean RC, Hoteit MA, et al. Combined heart and liver transplant: indication, patient selection, and allocation policy. Clin Liver Dis 2019; 13:170175.
Calne RY, Sells RA, Pena JR, et al. Induction of immunological tolerance by porcine liver allografts. Nature 1969; 223:472476.
Starzl TE, Demetris AJ, Trucco M, et al. Systemic chimerism in human female recipients of male livers. Lancet 1992; 340:876877.
Reyes J, Zeevi A, Ramos H, et al. Frequent achievement of a drug-free state after orthotopic liver transplantation. Transplant Proc 1993; 25:33153319.
Taner T, Heimbach JK, Rosen CB, et al. Decreased chronic cellular and antibody-mediated injury in the kidney following simultaneous liver-kidney transplantation. Kidney Int 2016; 89:909917.
Taner T, Gustafson MP, Hansen MJ, et al. Donor-specific hypo-responsiveness occurs in simultaneous liver-kidney transplant recipients after the first year. Kidney Int 2018; 93:14651474.
Abu-Elmagd K, Reyes J, Todo S, et al. Clinical intestinal transplantation: new perspectives and immunologic considerations. J Am Coll Surg 1998; 186:512525. discussion 525–527.
Grannas G, Neipp M, Hoeper MM, et al. Indications for and outcomes after combined lung and liver transplantation: a single-center experience on 13 consecutive cases. Transplantation 2008; 85:524531.
Gonwa TA, Nery JR, Husberg BS, et al. Simultaneous liver and renal transplantation in man. Transplantation 1988; 46:690693.
Olausson M, Mjörnstedt L, Nordén G, et al. Successful combined partial auxiliary liver and kidney transplantation in highly sensitized cross-match positive recipients. Am J Transplant 2007; 7:130136.
Fung J, Makowka L, Tzakis A, et al. Combined liver-kidney transplantation: analysis of patients with preformed lymphocytotoxic antibodies. Transplant Proc 1988; 20:8891.
Fong T-L, Bunnapradist S, Jordan SC, et al. Analysis of the United Network for Organ Sharing database comparing renal allografts and patient survival in combined liver-kidney transplantation with the contralateral allografts in kidney alone or kidney-pancreas transplantation. Transplantation 2003; 76:348353.
Braun W, Fung JJ. Can partial auxiliary liver transplantation protect kidney grafts in highly sensitized patients? Nat Clin Pract Nephrol 2007; 3:370371.
Simpson KM, Bunch DL, Amemiya H, et al. Humoral antibodies and coagulation mechanisms in the accelerated or hyperacute rejection of renal homografts in sensitized canine recipients. Surgery 1970; 68:7785.
Wu G, Cruz RJ. Liver-inclusive intestinal transplantation results in decreased alloimmune-mediated rejection but increased infection. Gastroenterol Rep 2018; 6:2937.
Pasupneti S, Lawrence A, Chhatwani L, et al. Combined lung-liver transplantation: the United States experience. J Heart Lung Transplant 2016; 35:S311.
Freischlag KW, Messina J, Ezekian B, et al. Single-center long-term analysis of combined liver-lung transplant outcomes. Transplant Direct 2018; 4:e349.
Atluri P, Gaffey A, Howard J, et al. Combined heart and liver transplantation can be safely performed with excellent short- and long-term results. Ann Thorac Surg 2014; 98:858862.
Raichlin E, Daly RC, Rosen CB, et al. Combined heart and liver transplantation: a single-center experience. Transplantation 2009; 88:219225.
Asrani SK, Warnes CA, Kamath PS. Hepatocellular carcinoma after the Fontan procedure. N Engl J Med 2013; 368:17561757.
D'Souza BA, Fuller S, Gleason LP, et al. Single-center outcomes of combined heart and liver transplantation in the failing Fontan. Clin Transplant 2017; 31:e12892.
Bryant R III, Morales D. Overview of adult congenital heart transplants. Ann Cardiothorac Surg 2018; 7:143151.
Careddu L, Zanfi C, Pantaleo A, et al. Combined heart–liver transplantation: a single-center experience. Transpl Int 2015; 28:828834.
Padegimas A, Molina M, Korwin A, et al. Successful long-term outcomes in combined heart–liver transplants across preformed high levels of donor-specific antibodies in highly sensitized patients. J Heart Lung Transplant 2016; 35:13821384.
Wong TW, Gandhi MJ, Daly RC, et al. Liver allograft provides immunoprotection for the cardiac allograft in combined heart–liver transplantation. Am J Transplant 2016; 16:35223531.
Chou AS, Habertheuer A, Chin AL, et al. Heart–kidney and heart–liver transplantation provide immunoprotection to the cardiac allograft. Ann Thorac Surg 2019; 108:458466.
Rana A, Robles S, Russo MJ, et al. The combined organ effect: protection against rejection? Ann Surg 2008; 248:871879.
Topilsky Y, Raichlin E, Hasin T, et al. Combined heart and liver transplant attenuates cardiac allograft vasculopathy compared with isolated heart transplantation. Transplantation 2013; 95:859865.
Das BB, Pruitt E, Molina K, et al. The impact of flow PRA on outcome in pediatric heart recipients in modern era: an analysis of the Pediatric Heart Transplant Study database. Pediatr Transplant 2018; 22:e13087.
Kidambi S, Mohamedali B, Bhat G. Clinical outcomes in sensitized heart transplant patients bridged with ventricular assist devices. Clin Transplant 2015; 29:499505.
Nwakanma LU, Williams JA, Weiss ES, et al. Influence of pretransplant panel-reactive antibody on outcomes in 8,160 heart transplant recipients in recent era. Ann Thorac Surg 2007; 8:15561562.
Scott V, Williams RJ, Levi DS. Outcomes of cardiac transplantation in highly sensitized pediatric patients. Pediatr Cardiol 2011; 32:615620.
Ortega-Legaspi JM, Molina MR, Quiaoit YA, et al. PRA is not associated with rejection in combined heart and liver transplantation. J Heart Lung Transplant 2020; 39:S31.
Daly RC, Pereira NL, Taner T, et al. Combined heart and liver transplantation in highly sensitized patients: protection of the cardiac allograft from antibody mediated rejection by initial liver implantation. J Heart Lung Transplant 2017; 36:S200.
Abrol N, Jadlowiec CC, Taner T. Revisiting liver's role in transplant alloimmunity. World J Gastroenterol 2019; 25:31233135.
Ahearn AJ, Klein I, Hayden T, et al. Liver transplant tolerance: differences in the persistence of various alloreactive T cell subsets. Transplantation 2010; 90:518.
Bettens F, Tiercy J-M, Campanile N, et al. Microchimerism after liver transplantation: absence of rejection without abrogation of antidonor cytotoxic T-lymphocyte–mediated alloreactivity. Liver Transpl 2005; 11:290297.
Bishop GA, Ierino FL, Sharland AF, et al. Approaching the promise of operational tolerance in clinical transplantation. Transplantation 2011; 91:10651074.
Ingelsten M, Karlsson-Parra A, Granqvist AB, et al. Postischemic inflammatory response in an auxiliary liver graft predicts renal graft outcome in sensitized patients. Transplantation 2011; 91:888894.
Bowen DG, Zen M, Holz L, et al. The site of primary T cell activation is a determinant of the balance between intrahepatic tolerance and immunity. J Clin Invest 2004; 114:701712.
Dangi A, Sumpter TL, Kimura S, et al. Selective expansion of allogeneic regulatory T cells by hepatic stellate cells: role of endotoxin and implications for allograft tolerance. J Immunol 2012; 188:36673677.
Huang H, Lu Y, Zhou T, et al. Innate immune cells in immune tolerance after liver transplantation. Front Immunol 2018; 9:2401.
Taner T, Gandhi MJ, Sanderson SO, et al. Prevalence, course and impact of HLA donor-specific antibodies in liver transplantation in the first year. Am J Transplant 2012; 12:15041510.
Chang DH, Kobashigawa JA. Desensitization strategies in the patient awaiting heart transplantation. Curr Opin Cardiol 2017; 32:301307.
Colvin MM, Cook JL, Chang PP, et al. Sensitization in heart transplantation: emerging knowledge: a scientific statement from the American Heart Association. Circulation 2019; 139:e553e578.

Auteurs

Juan M Ortega-Legaspi (JM)

Division of Cardiology, Advanced Heart Failure and Transplant Section.

Maarouf Hoteit (M)

Division of Gastroenterology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Joyce Wald (J)

Division of Cardiology, Advanced Heart Failure and Transplant Section.

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