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Granulocyte Transfusions in Patients with Chronic Granulomatous Disease Undergoing Hematopoietic Cell Transplantation or Gene Therapy.
Arnold, Danielle E; Chellapandian, Deepak; Parikh, Suhag; Mallhi, Kanwaldeep; Marsh, Rebecca A; Heimall, Jennifer R; Grossman, Debra; Chitty-Lopez, Maria; Murguia-Favela, Luis; Gennery, Andrew R; Boulad, Farid; Arbuckle, Erin; Cowan, Morton J; Dvorak, Christopher C; Griffith, Linda M; Haddad, Elie; Kohn, Donald B; Notarangelo, Luigi D; Pai, Sung-Yun; Puck, Jennifer M; Pulsipher, Michael A; Torgerson, Troy; Kang, Elizabeth M; Malech, Harry L; Leiding, Jennifer W.
Afiliación
  • Arnold DE; Immune Deficiency-Cellular Therapy Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Building 10-CRC, 1-5130, 10 Center Dr, Bethesda, MD, USA. danielle.arnold@nih.gov.
  • Chellapandian D; Center for Cell and Gene Therapy for Non-Malignant Conditions, Blood and Marrow Transplant Program, John Hopkins All Children's Hospital, St. Petersburg, FL, USA.
  • Parikh S; Division of Bone Marrow Transplant, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA.
  • Mallhi K; Fred Hutchinson Cancer Research Center, Seattle Children's Hospital, The University of Washington School of Medicine, Seattle, WA, USA.
  • Marsh RA; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Heimall JR; Division of Allergy and Immunology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Grossman D; Genetic Immunotherapy Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Chitty-Lopez M; Division of Allergy and Immunology, Department of Pediatrics, John Hopkins All Children's Hospital, University of South Florida, St. Petersburg, FL, USA.
  • Murguia-Favela L; Section of Hematology/Immunology, Department of Pediatrics, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Gennery AR; Translational and Clinical Research Institute, Newcastle University and Paediatric Immunology and Haematopoietic Stem Cell Transplantation, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Boulad F; Department of Pediatrics, BMT Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Arbuckle E; Department of Pediatrics, Duke University, Durham, NC, USA.
  • Cowan MJ; Division of Pediatric Allergy, Immunology, and Blood and Marrow Transplant, University of California San Francisco Benioff Children's Hospital, San Francisco, CA, USA.
  • Dvorak CC; Division of Pediatric Allergy, Immunology, and Blood and Marrow Transplant, University of California San Francisco Benioff Children's Hospital, San Francisco, CA, USA.
  • Griffith LM; Division of Allergy, Immunology and Transplantation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Haddad E; Immunology-Rheumatology Division, Department of Pediatrics, University of Montreal, Montreal, QC, Canada.
  • Kohn DB; Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at University of California, Los Angeles, CA, USA.
  • Notarangelo LD; Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Pai SY; Immune Deficiency-Cellular Therapy Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Building 10-CRC, 1-5130, 10 Center Dr, Bethesda, MD, USA.
  • Puck JM; Division of Pediatric Allergy, Immunology, and Blood and Marrow Transplant, University of California San Francisco Benioff Children's Hospital, San Francisco, CA, USA.
  • Pulsipher MA; Section of Transplantation and Cellular Therapy, Children's Hospital Los Angeles Cancer and Blood Disease Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Torgerson T; Experimental Immunology, Allen Institute, Seattle, WA, USA.
  • Kang EM; Genetic Immunotherapy Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Malech HL; Genetic Immunotherapy Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Leiding JW; Division of Allergy and Immunology, Department of Pediatrics, John Hopkins University, Baltimore, MD, USA.
J Clin Immunol ; 42(5): 1026-1035, 2022 07.
Article en En | MEDLINE | ID: mdl-35445907
ABSTRACT
Granulocyte transfusions are sometimes used as adjunctive therapy for the treatment of infection in patients with chronic granulomatous disease (CGD). However, granulocyte transfusions can be associated with a high rate of alloimmunization, and their role in CGD patients undergoing hematopoietic cell transplantation (HCT) or gene therapy (GT) is unknown. We identified 27 patients with CGD who received granulocyte transfusions pre- (within 6 months) and/or post-HCT or GT in a retrospective survey. Twelve patients received granulocyte transfusions as a bridge to cellular therapy. Six (50%) of these patients had a complete or partial response. However, six of 10 (60%) patients for whom testing was performed developed anti-HLA antibodies, and three of the patients also had severe immune-mediated cytopenia within the first 100 days post-HCT or GT. Fifteen patients received granulocyte transfusions post-HCT only. HLA antibodies were not checked for any of these 15 patients, but there were no cases of early immune-mediated cytopenia. Out of 25 patients who underwent HCT, there were 5 (20%) cases of primary graft failure. Three of the patients with primary graft failure had received granulocyte transfusions pre-HCT and were subsequently found to have anti-HLA antibodies. In this small cohort of patients with CGD, granulocyte transfusions pre-HCT or GT were associated with high rates of alloimmunization, primary graft failure, and early severe immune-mediated cytopenia post-HCT or GT. Granulocyte transfusions post-HCT do not appear to confer an increased risk of graft failure.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped / Enfermedad Granulomatosa Crónica Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Clin Immunol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped / Enfermedad Granulomatosa Crónica Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Clin Immunol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos