Antibody-Mediated Rejection in Liver Transplantation: Immuno-Pathological Characteristics and Long-Term Follow-Up.


Journal

Transplant international : official journal of the European Society for Organ Transplantation
ISSN: 1432-2277
Titre abrégé: Transpl Int
Pays: Switzerland
ID NLM: 8908516

Informations de publication

Date de publication:
2024
Historique:
received: 08 05 2024
accepted: 16 07 2024
medline: 13 9 2024
pubmed: 13 9 2024
entrez: 13 9 2024
Statut: epublish

Résumé

The diagnosis of liver antibody-mediated rejection (AMR) is challenging and likely under-recognized. The association of AMR with donor-specific antibodies (DSA), and its clinical course in relation to pathologic findings and treatment are ill defined. We identified cases of liver AMR by following the criteria outlined by the 2016 Banff Working Group. Patient demographics, native liver disease, histopathologic findings, treatment type, clinical outcome, and transaminase levels during AMR diagnosis, treatment, and resolution were determined. Patients (n = 8) with AMR average age was 55.2 years (range: 19-68). Seven of eight cases met the Banff criteria for AMR. Personalized treatment regimens consisted of optimization of immunosuppression, intravenous pulse steroids, plasmapheresis, IVIG, rituximab, and bortezomib. Five patients experienced complete resolution of AMR, return of transaminases to baseline, and decreased DSA at long-term follow-up. One patient developed chronic AMR and two patients required re-transplantation. Follow-up after AMR diagnosis ranged from one to 11 years. Because AMR can present at any time, crossmatch, early biopsy, and routine monitoring of DSA levels should be implemented following transaminase elevation to recognize AMR. Furthermore, treatment should be immediately implemented to reverse AMR and prevent graft failure, chronic damage, re-transplantation, and possibly mortality.

Identifiants

pubmed: 39267618
doi: 10.3389/ti.2024.13232
pii: 13232
pmc: PMC11391112
doi:

Substances chimiques

Isoantibodies 0
Immunosuppressive Agents 0
Rituximab 4F4X42SYQ6
Bortezomib 69G8BD63PP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

13232

Informations de copyright

Copyright © 2024 Cicalese, Walton, Du, Kulkarni, Qiu, El Hag and Stevenson.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Luca Cicalese (L)

Division of Transplant Surgery, Department of Surgery, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

Zachary C Walton (ZC)

John Sealy School of Medicine, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

Xiaotang Du (X)

Department of Pathology, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

Rupak Kulkarni (R)

Division of Transplant Surgery, Department of Surgery, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

Suimin Qiu (S)

Department of Pathology, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

Mohamed El Hag (M)

Department of Pathology, Cleveland Clinic, Cleveland, OH, United States.

Heather L Stevenson (HL)

Department of Pathology, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

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