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Author Notes:

Idelberto R. Badell, MD, Department of Surgery, Emory University School of Medicine, Woodruff Memorial Research Bldg, 101 Woodruff Cir, 5105 WMB, Atlanta, GA 30322. Email: ibadell@emory.edu

O.C. participated in research design, data collection, analysis, interpretation, and writing of the article. G.K. participated in data analysis and interpretation. W.H.K. and P.V. participated in data analysis, interpretation, and writing of the article. C.P.L. and I.R.B. participated in research design, data analysis, interpretation, and writing of the article.

Subject:

Keywords:

  • Kidney
  • Belatacept Conversion

Belatacept Conversion in Kidney After Liver Transplantation

Tools:

Journal Title:

Transplantation Direct

Volume:

Volume 7, Number 11

Publisher:

, Pages E780-E780

Type of Work:

Article | Final Publisher PDF

Abstract:

Background. Costimulatory blockade with belatacept has demonstrated long-term benefits in renal transplantation, but de novo use in liver transplant recipients has resulted in increased rejection, graft loss, and death. However, belatacept conversion as a calcineurin inhibitor (CNI) avoidance strategy has not been studied and may be of benefit in liver transplantation where CNI-induced renal dysfunction and toxicity are barriers to improved outcomes. Methods. Using clinical data extracted from our institutional medical record, we report on 8 patients who underwent kidney after liver transplantation and were treated with belatacept-based immunosuppression and transient CNI therapy. Results. All patients tolerated belatacept therapy without any patient deaths or graft losses. No episodes of rejection, de novo donor-specific antibody formation, or major systemic infections were observed, and all patients demonstrated preserved liver and excellent renal allograft function. Patients received belatacept for a median duration of 13.2 mo, and at a median follow-up of 15.9 mo post-kidney transplant, 6 of 8 patients continued on belatacept with 3 completely off and 3 poised to transition off CNI. Conclusions. These findings are the first evidence that in liver transplant recipients requiring subsequent kidney transplantation, belatacept-based therapy can potentially facilitate CNI-free maintenance immunosuppression. This supports the possibility of belatacept conversion in stand-alone liver transplant recipients as a viable method of CNI avoidance.

Copyright information:

© 2021 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/rdf).
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