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Automated Manufacture of Autologous CD19 CAR-T Cells for Treatment of Non-hodgkin Lymphoma.
Jackson, Zachary; Roe, Anne; Sharma, Ashish Arunkumar; Lopes, Filipa Blasco Tavares Pereira; Talla, Aarthi; Kleinsorge-Block, Sarah; Zamborsky, Kayla; Schiavone, Jennifer; Manjappa, Shivaprasad; Schauner, Robert; Lee, Grace; Liu, Ruifu; Caimi, Paolo F; Xiong, Ying; Krueger, Winfried; Worden, Andrew; Kadan, Mike; Schneider, Dina; Orentas, Rimas; Dropulic, Boro; Sekaly, Rafick-Pierre; de Lima, Marcos; Wald, David N; Reese, Jane S.
Afiliação
  • Jackson Z; Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
  • Roe A; Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
  • Sharma AA; Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
  • Lopes FBTP; Department of Nutrition, Case Western Reserve University, Cleveland, OH, United States.
  • Talla A; The Alan Turing Institute, British Library, London, United Kingdom.
  • Kleinsorge-Block S; Stem Cell Transplantation Program, University Hospitals Seidman Cancer Center, Cleveland, OH, United States.
  • Zamborsky K; Stem Cell Transplantation Program, University Hospitals Seidman Cancer Center, Cleveland, OH, United States.
  • Schiavone J; Stem Cell Transplantation Program, University Hospitals Seidman Cancer Center, Cleveland, OH, United States.
  • Manjappa S; Department of Medicine, University Hospitals Cleveland Medical Center, Cleveland, OH, United States.
  • Schauner R; Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
  • Lee G; Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
  • Liu R; Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
  • Caimi PF; Stem Cell Transplantation Program, University Hospitals Seidman Cancer Center, Cleveland, OH, United States.
  • Xiong Y; Department of Medicine, University Hospitals Cleveland Medical Center, Cleveland, OH, United States.
  • Krueger W; Lentigen Technology, Inc., a Miltenyi Biotec Company, Gaithersburg, MD, United States.
  • Worden A; Lentigen Technology, Inc., a Miltenyi Biotec Company, Gaithersburg, MD, United States.
  • Kadan M; Lentigen Technology, Inc., a Miltenyi Biotec Company, Gaithersburg, MD, United States.
  • Schneider D; Lentigen Technology, Inc., a Miltenyi Biotec Company, Gaithersburg, MD, United States.
  • Orentas R; Lentigen Technology, Inc., a Miltenyi Biotec Company, Gaithersburg, MD, United States.
  • Dropulic B; Department of Pediatrics, Seattle Children's Research Institute, Seattle, WA, United States.
  • Sekaly RP; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, United States.
  • de Lima M; Lentigen Technology, Inc., a Miltenyi Biotec Company, Gaithersburg, MD, United States.
  • Wald DN; Department of Pathology, Case Western Reserve University, Cleveland, OH, United States.
  • Reese JS; Stem Cell Transplantation Program, University Hospitals Seidman Cancer Center, Cleveland, OH, United States.
Front Immunol ; 11: 1941, 2020.
Article em En | MEDLINE | ID: mdl-32849651
ABSTRACT
Chimeric antigen receptor T cells (CAR-T cell) targeting CD19 are effective against several subtypes of CD19-expressing hematologic malignancies. Centralized manufacturing has allowed rapid expansion of this cellular therapy, but it may be associated with treatment delays due to the required logistics. We hypothesized that point of care manufacturing of CAR-T cells on the automated CliniMACS Prodigy® device allows reproducible and fast delivery of cells for the treatment of patients with non-Hodgkin lymphoma. Here we describe cell manufacturing results and characterize the phenotype and effector function of CAR-T cells used in a phase I/II study. We utilized a lentiviral vector delivering a second-generation CD19 CAR construct with 4-1BB costimulatory domain and TNFRSF19 transmembrane domain. Our data highlight the successful generation of CAR-T cells at numbers sufficient for all patients treated, a shortened duration of production from 12 to 8 days followed by fresh infusion into patients, and the detection of CAR-T cells in patient circulation up to 1-year post-infusion.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Linfócitos T / Imunoterapia Adotiva / Sistemas Automatizados de Assistência Junto ao Leito / Antígenos CD19 / Engenharia Celular / Receptores de Antígenos Quiméricos Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Linfócitos T / Imunoterapia Adotiva / Sistemas Automatizados de Assistência Junto ao Leito / Antígenos CD19 / Engenharia Celular / Receptores de Antígenos Quiméricos Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article