Your browser doesn't support javascript.
loading
DuoBody-CD40x4-1BB induces dendritic-cell maturation and enhances T-cell activation through conditional CD40 and 4-1BB agonist activity.
Muik, Alexander; Adams 3rd, Homer C; Gieseke, Friederike; Altintas, Isil; Schoedel, Kristina B; Blum, Jordan M; Sänger, Bianca; Burm, Saskia M; Stanganello, Eliana; Verzijl, Dennis; Spires, Vanessa M; Vascotto, Fulvia; Toker, Aras; Quinkhardt, Juliane; Fereshteh, Mark; Diken, Mustafa; Satijn, David P E; Kreiter, Sebastian; Ahmadi, Tahamtan; Breij, Esther C W; Türeci, Özlem; Sasser, Kate; Sahin, Ugur; Jure-Kunkel, Maria.
Afiliación
  • Muik A; BioNTech SE, Mainz, Germany.
  • Adams 3rd HC; Genmab US Inc, Plainsboro, New Jersey, USA.
  • Gieseke F; BioNTech SE, Mainz, Germany.
  • Altintas I; Translational Research and Precision Medicine, Genmab BV, Utrecht, The Netherlands.
  • Schoedel KB; BioNTech SE, Mainz, Germany.
  • Blum JM; Genmab US Inc, Plainsboro, New Jersey, USA.
  • Sänger B; BioNTech SE, Mainz, Germany.
  • Burm SM; Translational Research and Precision Medicine, Genmab BV, Utrecht, The Netherlands.
  • Stanganello E; TRON-Translational Oncology at the University Medical Center of the Johannes Gutenberg University gGmbH, Mainz, Germany.
  • Verzijl D; Translational Research and Precision Medicine, Genmab BV, Utrecht, The Netherlands.
  • Spires VM; Genmab US Inc, Plainsboro, New Jersey, USA.
  • Vascotto F; TRON-Translational Oncology at the University Medical Center of the Johannes Gutenberg University gGmbH, Mainz, Germany.
  • Toker A; BioNTech SE, Mainz, Germany.
  • Quinkhardt J; BioNTech SE, Mainz, Germany.
  • Fereshteh M; Genmab US Inc, Plainsboro, New Jersey, USA.
  • Diken M; BioNTech SE, Mainz, Germany.
  • Satijn DPE; Genmab BV, Utrecht, The Netherlands.
  • Kreiter S; BioNTech SE, Mainz, Germany.
  • Ahmadi T; Experimental Medicine, Genmab US Inc, Plainsboro, New Jersey, USA.
  • Breij ECW; Translational Research and Precision Medicine, Genmab BV, Utrecht, The Netherlands.
  • Türeci Ö; BioNTech SE, Mainz, Germany.
  • Sasser K; Genmab US Inc, Plainsboro, New Jersey, USA.
  • Sahin U; BioNTech SE, Mainz, Germany.
  • Jure-Kunkel M; TRON-Translational Oncology at the University Medical Center of the Johannes Gutenberg University gGmbH, Mainz, Germany.
J Immunother Cancer ; 10(6)2022 06.
Article en En | MEDLINE | ID: mdl-35688554
BACKGROUND: Despite the preclinical promise of CD40 and 4-1BB as immuno-oncology targets, clinical efforts evaluating CD40 and 4-1BB agonists as monotherapy have found limited success. DuoBody-CD40×4-1BB (GEN1042/BNT312) is a novel investigational Fc-inert bispecific antibody for dual targeting and conditional stimulation of CD40 and 4-1BB to enhance priming and reactivation of tumor-specific immunity in patients with cancer. METHODS: Characterization of DuoBody-CD40×4-1BB in vitro was performed in a broad range of functional immune cell assays, including cell-based reporter assays, T-cell proliferation assays, mixed-lymphocyte reactions and tumor-infiltrating lymphocyte assays, as well as live-cell imaging. The in vivo activity of DuoBody-CD40×4-1BB was assessed in blood samples from patients with advanced solid tumors that were treated with DuoBody-CD40×4-1BB in the dose-escalation phase of the first-in-human clinical trial (NCT04083599). RESULTS: DuoBody-CD40×4-1BB exhibited conditional CD40 and 4-1BB agonist activity that was strictly dependent on crosslinking of both targets. Thereby, DuoBody-CD40×4-1BB strengthened the dendritic cell (DC)/T-cell immunological synapse, induced DC maturation, enhanced T-cell proliferation and effector functions in vitro and enhanced expansion of patient-derived tumor-infiltrating lymphocytes ex vivo. The addition of PD-1 blocking antibodies resulted in potentiation of T-cell activation and effector functions in vitro compared with either monotherapy, providing combination rationale. Furthermore, in a first-in-human clinical trial, DuoBody-CD40×4-1BB mediated clear immune modulation of peripheral antigen presenting cells and T cells in patients with advanced solid tumors. CONCLUSION: DuoBody-CD40×4-1BB is capable of enhancing antitumor immunity by modulating DC and T-cell functions and shows biological activity in patients with advanced solid tumors. These findings demonstrate that targeting of these two pathways with an Fc-inert bispecific antibody may be an efficacious approach to (re)activate tumor-specific immunity and support the clinical investigation of DuoBody-CD40×4-1BB for the treatment of cancer.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anticuerpos Biespecíficos / Neoplasias Límite: Humans Idioma: En Revista: J Immunother Cancer Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anticuerpos Biespecíficos / Neoplasias Límite: Humans Idioma: En Revista: J Immunother Cancer Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido