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Natural Antibodies Are Associated With Rejection and Long-term Renal Allograft Loss in a Multicenter International Cohort.
See, Sarah B; Yang, Xue; Burger, Carole; Lamarthée, Baptiste; Snanoudj, Renaud; Shihab, Ronzon; Tsapepas, Demetra S; Roy, Poulomi; Larivière-Beaudoin, Stéphanie; Hamelin, Katia; Mendoza Rojas, Aleixandra; van Besouw, Nicole M; Bartosic, Amanda; Daniel, Nikita; Rodica, Vasilescu E; Mohan, Sumit; Cohen, David; Ratner, Lloyd; Baan, Carla C; Bromberg, Jonathan S; Cardinal, Héloïse; Anglicheau, Dany; Sun, Yifei; Zorn, Emmanuel.
Affiliation
  • See SB; Columbia Center for Translational Immunology, Columbia University Irving Medical Center, NY.
  • Yang X; Department of Biostatistics, Columbia University Irving Medical Center, NY.
  • Burger C; Department of Kidney Transplantation, Hôpital Universitaire Necker-Assistance Publique Hopitaux de Paris, France.
  • Lamarthée B; Necker-Enfants Malades Institute, Inserm U1151, Université de Paris, Paris, France.
  • Snanoudj R; Department of Kidney Transplantation, Hôpital Kremlin Bicêtre, Paris, France.
  • Shihab R; Columbia Center for Translational Immunology, Columbia University Irving Medical Center, NY.
  • Tsapepas DS; Department of Surgery, Columbia University Vagelos College of Physicians and Surgeons, NY.
  • Roy P; Columbia Center for Translational Immunology, Columbia University Irving Medical Center, NY.
  • Larivière-Beaudoin S; Research Center, Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.
  • Hamelin K; Canadian Donation and Transplantation Research Program, Edmonton, AB, Canada.
  • Mendoza Rojas A; Research Center, Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.
  • van Besouw NM; Department of Internal Medicine - Nephrology and Transplantation, Transplant Institute, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Bartosic A; Department of Internal Medicine - Nephrology and Transplantation, Transplant Institute, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Daniel N; Department of Surgery, University of Maryland School of Medicine, BaltimoreMD.
  • Rodica VE; Department of Surgery, University of Maryland School of Medicine, BaltimoreMD.
  • Mohan S; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, NY.
  • Cohen D; Department of Medicine, Division of Nephrology, Columbia University Vagelos College of Physicians and Surgeons, NY.
  • Ratner L; Department of Epidemiology, Columbia University Mailman School of Public Health, NY.
  • Baan CC; Department of Medicine, Division of Nephrology, Columbia University Vagelos College of Physicians and Surgeons, NY.
  • Bromberg JS; Department of Medicine, Division of Nephrology, Columbia University Vagelos College of Physicians and Surgeons, NY.
  • Cardinal H; Department of Internal Medicine - Nephrology and Transplantation, Transplant Institute, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Anglicheau D; Department of Surgery, University of Maryland School of Medicine, BaltimoreMD.
  • Sun Y; Research Center, Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada.
  • Zorn E; Canadian Donation and Transplantation Research Program, Edmonton, AB, Canada.
Transplantation ; 107(7): 1580-1592, 2023 07 01.
Article de En | MEDLINE | ID: mdl-36728359
ABSTRACT

BACKGROUND:

Potentially harmful nonhuman leukocyte antigen antibodies have been identified in renal transplantation, including natural immunoglobulin G antibodies (Nabs) reactive to varied antigenic structures, including apoptotic cells.

METHODS:

In this retrospective, multicenter study, we assessed Nabs by reactivity to apoptotic cells in sera collected from 980 kidney transplant recipients across 4 centers to determine their association with graft outcomes.

RESULTS:

Elevated pretransplant Nabs were associated with graft loss (hazard ratio [HR] 2.71; 95% confidence interval [CI], 1.15-6.39; P = 0.0232), the composite endpoint of graft loss or severe graft dysfunction (HR 2.40; 95% CI, 1.13-5.10; P = 0.0232), and T cell-mediated rejection (odds ratio [OR] 1.77; 95% CI, 1.07-3.02; P = 0.0310). High pretransplant Nabs together with donor-specific antibodies (DSAs) were associated with increased risk of composite outcomes (HR 6.31; 95% CI, 1.81-22.0; P = 0.0039). In patients with high pretransplant Nabs, the subsequent development of posttransplant Nabs was associated with both T cell-mediated rejection (OR 3.64; 95% CI, 1.61-8.36; P = 0.0021) and mixed rejection (OR 3.10; 95% CI, 1.02-9.75; P = 0.0473). Finally, elevated pre- and posttransplant Nabs combined with DSAs were associated with increased risk of composite outcomes (HR 3.97; 95% CI, 1.51-10.43; P = 0.0052) and T cell-mediated rejection (OR 7.28; 95% CI, 2.16-25.96; P = 0.0016).

CONCLUSIONS:

The presence of pre- and posttransplant Nabs, together with DSAs, was associated with increased risk of poor graft outcomes and rejection after renal transplantation.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Transplantation rénale Type d'étude: Clinical_trials / Observational_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Transplantation Année: 2023 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Transplantation rénale Type d'étude: Clinical_trials / Observational_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Transplantation Année: 2023 Type de document: Article
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