Lack of Association between Pretransplant Donor-Specific Antibodies and Posttransplant Kidney Outcomes in Simultaneous Liver-Kidney Transplant Recipients with Rabbit Anti-Thymocyte Globulin Induction and Steroid-Free Protocol.


Journal

Nephron
ISSN: 2235-3186
Titre abrégé: Nephron
Pays: Switzerland
ID NLM: 0331777

Informations de publication

Date de publication:
2020
Historique:
received: 25 09 2019
accepted: 15 12 2019
pubmed: 3 2 2020
medline: 9 3 2021
entrez: 3 2 2020
Statut: ppublish

Résumé

The impact of pretransplant donor-specific antibodies (DSAs), especially class II DSAs, on kidney allograft outcomes remains unclear in simultaneous liver-kidney transplantation (SLKT) recipients. We examined 85 recipients who consecutively underwent SLKT between 2009 and 2018 in our center. Associations between pretransplant DSA and worsening kidney function (WKF), kidney allograft loss, composite kidney outcome (WKF and/or antibody-mediated rejection and/or death-censored kidney allograft loss), death with functioning graft, and overall mortality were examined in survival analysis. WKF was defined as an eGFR decrease of 30% or greater from baseline, or 2 or more episodes of proteinuria, at least 90 days apart from each other. The mean age at SLKT was 56 ± 10 years, and 62% of the recipients were male. More than one quarter (26%) of our recipients were African American. The 2 major causes of end-stage liver disease were hepatitis C (28%) and alcoholic hepatitis (26%). Nineteen recipients (22%) had pretransplant DSAs at the time of SLKT. The DSA(+) group and DSA(-) group had similar risk of WKF (unadjusted model: hazard ratio [HR] = 0.77, 95% confidence interval [CI]: 0.29-2.05 and adjusted model: HR = 0.36, 95% CI: 0.12-1.08); similar risk of composite kidney outcome (unadjusted model: HR = 1.04, 95% CI: 0.45-2.43 and adjusted model: HR = 0.53, 95% CI: 0.20-1.39); and similar risk of overall death (unadjusted model: HR = 1.23, 95% CI: 0.45-3.36 and adjusted model: HR = 1.28, 95% CI: 0.42-3.87). We found similar results when comparing different DSA subclasses (class I and II DSAs) with recipients without DSAs. The presence of pretransplant DSAs was not associated with worse kidney allograft outcomes from our single-center experience. Further prospective larger studies are strongly warranted.

Identifiants

pubmed: 32007998
pii: 000505460
doi: 10.1159/000505460
doi:

Substances chimiques

Antilymphocyte Serum 0
Histocompatibility Antigens Class II 0
Isoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

126-137

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Masahiko Yazawa (M)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Division of Nephrology and Hypertension, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.

Orsolya Cseprekal (O)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Department of Transplantation and Surgery, Semmelweis University, Budapest, Hungary.

Ryan A Helmick (RA)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Manish Talwar (M)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Vasanthi Balaraman (V)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Pradeep S B Podila (PSB)

Faith & Health Division, Methodist Le Bonheur Healthcare, Memphis, Tennessee, USA.
Division of Health Systems Management & Policy, School of Public Health, The University of Memphis, Memphis, Tennessee, USA.

Uchenna A Agbim (UA)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Benedict Maliakkal (B)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Sallyanne Fossey (S)

Transplant Immunology Laboratory, DCI Inc., Nashville, Tennessee, USA.

Sanjaya K Satapathy (SK)

Sandra Atlas Bass Center for Liver Diseases & Transplantation, Department of Medicine, Northshore University Hospital/Northwell Health, Manhasset, New York, USA.

Keiichi Sumida (K)

Division of Nephrology, Department of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Csaba P Kovesdy (CP)

Division of Nephrology, Department of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Nephrology Section, Memphis Veterans Affairs Medical Center, Memphis, Tennessee, USA.

Satheesh Nair (S)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

James D Eason (JD)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Miklos Z Molnar (MZ)

James D. Eason Transplant Institute, Methodist University Hospital, Memphis, Tennessee, USA, mzmolnar@uthsc.edu.
Division of Transplant Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA, mzmolnar@uthsc.edu.
Department of Transplantation and Surgery, Semmelweis University, Budapest, Hungary, mzmolnar@uthsc.edu.
Division of Nephrology, Department of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA, mzmolnar@uthsc.edu.

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