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Specific Class I HLA Supertypes but Not HLA Zygosity or Expression Are Associated with Outcomes following HLA-Matched Allogeneic Hematopoietic Cell Transplant: HLA Supertypes Impact Allogeneic HCT Outcomes.
Camacho-Bydume, Christine; Wang, Tao; Sees, Jennifer A; Fernandez-Viña, Marcelo; Abid, Muhammad Bilal; Askar, Medhat; Beitinjaneh, Amer; Brown, Valerie; Castillo, Paul; Chhabra, Saurabh; Gadalla, Shahinaz M; Hsu, Jing-Mei; Kamoun, Malek; Lazaryan, Aleksandr; Nishihori, Taiga; Page, Kristin; Schetelig, Johannes; Fleischhauer, Katharina; Marsh, Steven G E; Paczesny, Sophie; Spellman, Stephen R; Lee, Stephanie J; Hsu, Katharine C.
Afiliación
  • Camacho-Bydume C; Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Wang T; Division of Biostatistics, Medical College of Wisconsin, Milwaukee, WI.
  • Sees JA; Center for International Blood and Marrow Transplant Research, National Marrow Donor Program/Be The Match, Minneapolis, MN.
  • Fernandez-Viña M; Department of Pathology, Stanford University School of Medicine, Stanford, CA.
  • Abid MB; Divisions of Hematology/Oncology and Infectious Diseases, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
  • Askar M; Department of Pathology and Laboratory Medicine, Baylor University Medical Center, Dallas, Texas.
  • Beitinjaneh A; Department of Medicine, Division of Transplantation and Cellular Therapy, University of Miami, Miami, Florida.
  • Brown V; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Penn State Hershey Children's Hospital and College of Medicine, Hershey, Pennsylvania.
  • Castillo P; Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Florida Health Shands Children's Hospital, Gainesville, FL.
  • Chhabra S; Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
  • Gadalla SM; Division of Cancer Epidemiology & Genetics, NIH-NCI Clinical Genetics Branch, Rockville, Maryland.
  • Hsu JM; Division of Hematology/Oncology, Department of Medicine, Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine/New York Presbyterian Hospital, New York, NY.
  • Kamoun M; Deparment of Pathology and Laboratory Medicine, Perelman School of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA.
  • Lazaryan A; Department of Blood and Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, Florida.
  • Nishihori T; Department of Blood and Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, Florida.
  • Page K; Division of Pediatric Blood and Marrow Transplantation, Duke University Medical Center, Durham, North Carolina.
  • Schetelig J; Department of Internal Medicine I, University Hospital Carl Gustav Carus Dresden, Dresden, Germany.
  • Fleischhauer K; Institute for Experimental Cellular Therapy, University Hospital Essen, Essen, Germany.
  • Marsh SGE; Anthony Nolan Research Institute, Royal Free Hospital, London, UK; UCL Cancer Institute, London, UK.
  • Paczesny S; Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC.
  • Spellman SR; Center for International Blood and Marrow Transplant Research, National Marrow Donor Program/Be The Match, Minneapolis, MN.
  • Lee SJ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Department of Medicine, University of Washington, Seattle, WA.
  • Hsu KC; Department of Medicine, Adult Bone Marrow Transplantation Service, Memorial Sloan Kettering Cancer Center, New York, New York; Department of Medicine, Weill Cornell Medical College, New York, New York; Human Oncology & Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New Y
Transplant Cell Ther ; 27(2): 142.e1-142.e11, 2021 02.
Article en En | MEDLINE | ID: mdl-33053450
ABSTRACT
Maximizing the probability of antigen presentation to T cells through diversity in HLAs can enhance immune responsiveness and translate into improved clinical outcomes, as evidenced by the association of heterozygosity and supertypes at HLA class I loci with improved survival in patients with advanced solid tumors treated with immune checkpoint inhibitors. We investigated the impact of HLA heterozygosity, supertypes, and surface expression on outcomes in adult and pediatric patients with acute myeloid leukemia (AML), myelodysplastic syndrome, acute lymphoblastic leukemia, and non-Hodgkin lymphoma who underwent 8/8 HLA-matched, T cell replete, unrelated, allogeneic hematopoietic cell transplant (HCT) from 2000 to 2015 using patient data reported to the Center for International Blood and Marrow Transplant Research. HLA class I heterozygosity and HLA expression were not associated with overall survival, relapse, transplant-related mortality (TRM), disease-free survival (DFS), and acute graft-versus-host disease following HCT. The HLA-B62 supertype was associated with decreased TRM in the entire patient cohort (hazard ratio [HR], 0.79; 95% CI, 0.69 to 0.90; P = .00053). The HLA-B27 supertype was associated with worse DFS in patients with AML (HR = 1.21; 95% CI, 1.10 to 1.32; P = .00005). These findings suggest that the survival benefit of HLA heterozygosity seen in solid tumor patients receiving immune checkpoint inhibitors does not extend to patients undergoing allogeneic HCT. Certain HLA supertypes, however, are associated with TRM and DFS, suggesting that similarities in peptide presentation between supertype members play a role in these outcomes. Beyond implications for prognosis following HCT, these findings support the further investigation of these HLA supertypes and the specific immune peptides important for transplant outcomes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Humans Idioma: En Revista: Transplant Cell Ther Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Humans Idioma: En Revista: Transplant Cell Ther Año: 2021 Tipo del documento: Article
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