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Complement-activating donor-specific anti-HLA antibodies and solid organ transplant survival: A systematic review and meta-analysis.
Bouquegneau, Antoine; Loheac, Charlotte; Aubert, Olivier; Bouatou, Yassine; Viglietti, Denis; Empana, Jean-Philippe; Ulloa, Camilo; Murad, Mohammad Hassan; Legendre, Christophe; Glotz, Denis; Jackson, Annette M; Zeevi, Adriana; Schaub, Stephan; Taupin, Jean-Luc; Reed, Elaine F; Friedewald, John J; Tyan, Dolly B; Süsal, Caner; Shapiro, Ron; Woodle, E Steve; Hidalgo, Luis G; O'Leary, Jacqueline; Montgomery, Robert A; Kobashigawa, Jon; Jouven, Xavier; Jabre, Patricia; Lefaucheur, Carmen; Loupy, Alexandre.
Afiliação
  • Bouquegneau A; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Loheac C; Department of Nephrology, Dialysis and Transplantation, CHU de Liège, Liège, Belgium.
  • Aubert O; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Bouatou Y; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Viglietti D; Department of Kidney Transplantation, Necker Hospital, Paris Descartes University, and Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Empana JP; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Ulloa C; Division of Nephrology, Geneva University Hospitals, Geneva, Switzerland.
  • Murad MH; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Legendre C; Department of Nephrology and Kidney Transplantation, Saint-Louis Hospital, Paris Diderot University, AP-HP, Paris, France.
  • Glotz D; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Jackson AM; Hospital Barros Luco Trudeau, Santiago, Chile et Clinica Alemana de Santiago, Chile.
  • Zeevi A; Mayo Clinic Evidence-based Practice Center, Mayo Clinic, Rochester, Minnesota, United States of America.
  • Schaub S; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Taupin JL; Department of Kidney Transplantation, Necker Hospital, Paris Descartes University, and Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Reed EF; Paris Translational Research Center for Organ Transplantation INSERM Unit 970, Paris, France.
  • Friedewald JJ; Department of Nephrology and Kidney Transplantation, Saint-Louis Hospital, Paris Diderot University, AP-HP, Paris, France.
  • Tyan DB; Immunogenetics Laboratory, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Süsal C; Department of Pathology, Surgery and Immunology at University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States of America.
  • Shapiro R; Clinic for Transplantation Immunology and Nephrology, University Hospital Basel, Basel, Switzerland.
  • Woodle ES; Department of Immunology and Histocompatibility, CHU Paris-GH St-Louis Lariboisière, Paris, France.
  • Hidalgo LG; Department of Pathology and Laboratory Medicine, UCLA Immunogenetics Center, David Geffen School of Medicine, University of California, Los Angeles, California, United States of America.
  • O'Leary J; Northwestern University Feinberg School of Medicine, Comprehensive Transplant Center, Division of Transplant Surgery, Chicago, Illinois, United states of America.
  • Montgomery RA; Division of Nephrology, Department of Medicine, Stanford University, Stanford, California, United States of America.
  • Kobashigawa J; Institute of Immunology, Heidelberg University, Department of Transplantation Immunology, Heidelberg, Germany.
  • Jouven X; Kidney/Pancreas Transplant Program, Mount Sinai Hospital, Recanati Miller Transplantation Institute, New York, New York, United States of America.
  • Jabre P; Division of Transplantation, Department of Surgery, and Division of Hematology and Oncology, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio, United States of America.
  • Lefaucheur C; Department of Laboratory Medicine and Pathology and Alberta Transplant Applied Genomics Center, Edmonton, Alberta, Canada.
  • Loupy A; Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, Texas, United States of America.
PLoS Med ; 15(5): e1002572, 2018 05.
Article em En | MEDLINE | ID: mdl-29799874
BACKGROUND: Anti-human leukocyte antigen donor-specific antibodies (anti-HLA DSAs) are recognized as a major barrier to patients' access to organ transplantation and the major cause of graft failure. The capacity of circulating anti-HLA DSAs to activate complement has been suggested as a potential biomarker for optimizing graft allocation and improving the rate of successful transplantations. METHODS AND FINDINGS: To address the clinical relevance of complement-activating anti-HLA DSAs across all solid organ transplant patients, we performed a meta-analysis of their association with transplant outcome through a systematic review, from inception to January 31, 2018. The primary outcome was allograft loss, and the secondary outcome was allograft rejection. A comprehensive search strategy was conducted through several databases (Medline, Embase, Cochrane, and Scopus). A total of 5,861 eligible citations were identified. A total of 37 studies were included in the meta-analysis. Studies reported on 7,936 patients, including kidney (n = 5,991), liver (n = 1,459), heart (n = 370), and lung recipients (n = 116). Solid organ transplant recipients with circulating complement-activating anti-HLA DSAs experienced an increased risk of allograft loss (pooled HR 3.09; 95% CI 2.55-3.74, P = 0.001; I2 = 29.3%), and allograft rejection (pooled HR 3.75; 95% CI: 2.05-6.87, P = 0.001; I2 = 69.8%) compared to patients without complement-activating anti-HLA DSAs. The association between circulating complement-activating anti-HLA DSAs and allograft failure was consistent across all subgroups and sensitivity analyses. Limitations of the study are the observational and retrospective design of almost all included studies, the higher proportion of kidney recipients compared to other solid organ transplant recipients, and the inclusion of fewer studies investigating allograft rejection. CONCLUSIONS: In this study, we found that circulating complement-activating anti-HLA DSAs had a significant deleterious impact on solid organ transplant survival and risk of rejection. The detection of complement-activating anti-HLA DSAs may add value at an individual patient level for noninvasive biomarker-guided risk stratification. TRIAL REGISTRATION: National Clinical Trial protocol ID: NCT03438058.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunologia de Transplantes / Ativação do Complemento / Sobrevivência de Enxerto / Antígenos HLA / Anticorpos Tipo de estudo: Guideline / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: PLoS Med Assunto da revista: MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunologia de Transplantes / Ativação do Complemento / Sobrevivência de Enxerto / Antígenos HLA / Anticorpos Tipo de estudo: Guideline / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: PLoS Med Assunto da revista: MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França