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Pre-clinical validation of a pan-cancer CAR-T cell immunotherapy targeting nfP2X7.
Bandara, Veronika; Foeng, Jade; Gundsambuu, Batjargal; Norton, Todd S; Napoli, Silvana; McPeake, Dylan J; Tyllis, Timona S; Rohani-Rad, Elaheh; Abbott, Caitlin; Mills, Stuart J; Tan, Lih Y; Thompson, Emma J; Willet, Vasiliki M; Nikitaras, Victoria J; Zheng, Jieren; Comerford, Iain; Johnson, Adam; Coombs, Justin; Oehler, Martin K; Ricciardelli, Carmela; Cowin, Allison J; Bonder, Claudine S; Jensen, Michael; Sadlon, Timothy J; McColl, Shaun R; Barry, Simon C.
Afiliação
  • Bandara V; Molecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.
  • Foeng J; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Gundsambuu B; Molecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.
  • Norton TS; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Napoli S; Molecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.
  • McPeake DJ; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Tyllis TS; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Rohani-Rad E; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Abbott C; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Mills SJ; University of South Australia, STEM (Future Industries Institute) SA, Adelaide, 5095, Australia.
  • Tan LY; Centre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, 5001, Australia.
  • Thompson EJ; Centre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, 5001, Australia.
  • Willet VM; Reproductive Cancer Research Group, Discipline Obstetrics and Gynaecology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Nikitaras VJ; Reproductive Cancer Research Group, Discipline Obstetrics and Gynaecology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Zheng J; Molecular Immunology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5000, Australia.
  • Comerford I; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Johnson A; Seattle Children's Research Institute, Seattle, WA, 98101, USA.
  • Coombs J; Carina Biotech, Level 2 Innovation & Collaboration Centre, UniSA Bradley Building, Adelaide, SA, 5001, Australia.
  • Oehler MK; Department of Gynaecological Oncology, Royal Adelaide Hospital, Adelaide, SA, 5005, Australia.
  • Ricciardelli C; Reproductive Cancer Research Group, Discipline Obstetrics and Gynaecology, Robinson Research Institute, University of Adelaide, Adelaide, SA, 5005, Australia.
  • Cowin AJ; University of South Australia, STEM (Future Industries Institute) SA, Adelaide, 5095, Australia.
  • Bonder CS; Centre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, SA, 5001, Australia.
  • Jensen M; Adelaide Medical School, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Sadlon TJ; Seattle Children's Research Institute, Seattle, WA, 98101, USA.
  • McColl SR; Department of Gastroenterology, Women's and Children's Health Network, North Adelaide, SA, 5006, Australia.
  • Barry SC; Chemokine Biology Laboratory, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, SA, 5005, Australia.
Nat Commun ; 14(1): 5546, 2023 09 08.
Article em En | MEDLINE | ID: mdl-37684239
ABSTRACT
Chimeric antigen receptor (CAR)-T cell immunotherapy is a novel treatment that genetically modifies the patients' own T cells to target and kill malignant cells. However, identification of tumour-specific antigens expressed on multiple solid cancer types, remains a major challenge. P2X purinoceptor 7 (P2X7) is a cell surface expressed ATP gated cation channel, and a dysfunctional version of P2X7, named nfP2X7, has been identified on cancer cells from multiple tissues, while being undetectable on healthy cells. We present a prototype -human CAR-T construct targeting nfP2X7 showing potential antigen-specific cytotoxicity against twelve solid cancer types (breast, prostate, lung, colorectal, brain and skin). In xenograft mouse models of breast and prostate cancer, CAR-T cells targeting nfP2X7 exhibit robust anti-tumour efficacy. These data indicate that nfP2X7 is a suitable immunotherapy target because of its broad expression on human tumours. CAR-T cells targeting nfP2X7 have potential as a wide-spectrum cancer immunotherapy for solid tumours in humans.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata Limite: Animals / Humans / Male Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata Limite: Animals / Humans / Male Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália