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Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies.
Arce Vargas, Frederick; Furness, Andrew J S; Litchfield, Kevin; Joshi, Kroopa; Rosenthal, Rachel; Ghorani, Ehsan; Solomon, Isabelle; Lesko, Marta H; Ruef, Nora; Roddie, Claire; Henry, Jake Y; Spain, Lavinia; Ben Aissa, Assma; Georgiou, Andrew; Wong, Yien Ning Sophia; Smith, Myles; Strauss, Dirk; Hayes, Andrew; Nicol, David; O'Brien, Tim; Mårtensson, Linda; Ljungars, Anne; Teige, Ingrid; Frendéus, Björn; Pule, Martin; Marafioti, Teresa; Gore, Martin; Larkin, James; Turajlic, Samra; Swanton, Charles; Peggs, Karl S; Quezada, Sergio A.
Afiliação
  • Arce Vargas F; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Furness AJS; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Litchfield K; Translational Cancer Therapeutics Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Joshi K; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Rosenthal R; Bill Lyons Informatics Centre, UCL Cancer Institute, London WC1E 6DD, UK; Cancer Research UK Lung Cancer Centre of Excellence, UCL Cancer Institute, London WC1E 6DD, UK.
  • Ghorani E; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Solomon I; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Lesko MH; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Ruef N; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Roddie C; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Henry JY; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Spain L; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Ben Aissa A; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Georgiou A; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Wong YNS; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Smith M; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Strauss D; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Hayes A; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Nicol D; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • O'Brien T; Guy's and St Thomas' NHS Foundation Trust, London SE1 9RT, UK.
  • Mårtensson L; BioInvent International AB, 223 70 Lund, Sweden.
  • Ljungars A; BioInvent International AB, 223 70 Lund, Sweden.
  • Teige I; BioInvent International AB, 223 70 Lund, Sweden.
  • Frendéus B; BioInvent International AB, 223 70 Lund, Sweden.
  • Pule M; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK.
  • Marafioti T; Department of Cellular Pathology, University College London Hospital, London NW1 2BU, UK.
  • Gore M; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Larkin J; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
  • Turajlic S; The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK; Translational Cancer Therapeutics Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Swanton C; Translational Cancer Therapeutics Laboratory, The Francis Crick Institute, London NW1 1AT, UK; Cancer Research UK Lung Cancer Centre of Excellence, UCL Cancer Institute, London WC1E 6DD, UK; Translational Cancer Therapeutics Laboratory, UCL Cancer Institute, London WC1E 6DD, UK.
  • Peggs KS; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK. Electronic address: k.peggs@ucl.ac.uk.
  • Quezada SA; Cancer Immunology Unit, University College London (UCL) Cancer Institute, London WC1E 6DD, UK; Research Department of Haematology, UCL Cancer Institute, London WC1E 6DD, UK. Electronic address: s.quezada@ucl.ac.uk.
Cancer Cell ; 33(4): 649-663.e4, 2018 04 09.
Article em En | MEDLINE | ID: mdl-29576375
With the use of a mouse model expressing human Fc-gamma receptors (FcγRs), we demonstrated that antibodies with isotypes equivalent to ipilimumab and tremelimumab mediate intra-tumoral regulatory T (Treg) cell depletion in vivo, increasing the CD8+ to Treg cell ratio and promoting tumor rejection. Antibodies with improved FcγR binding profiles drove superior anti-tumor responses and survival. In patients with advanced melanoma, response to ipilimumab was associated with the CD16a-V158F high affinity polymorphism. Such activity only appeared relevant in the context of inflamed tumors, explaining the modest response rates observed in the clinical setting. Our data suggest that the activity of anti-CTLA-4 in inflamed tumors may be improved through enhancement of FcγR binding, whereas poorly infiltrated tumors will likely require combination approaches.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de IgG / Linfócitos T Reguladores / Polimorfismo de Nucleotídeo Único / Antineoplásicos Imunológicos / Melanoma Limite: Animals / Female / Humans Idioma: En Revista: Cancer Cell Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de IgG / Linfócitos T Reguladores / Polimorfismo de Nucleotídeo Único / Antineoplásicos Imunológicos / Melanoma Limite: Animals / Female / Humans Idioma: En Revista: Cancer Cell Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos