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CD19-CD28: an affinity-optimized CD28 agonist for combination with glofitamab (CD20-TCB) as off-the-shelf immunotherapy.
Sam, Johannes; Hofer, Thomas; Kuettel, Christine; Claus, Christina; Thom, Jenny; Herter, Sylvia; Georges, Guy; Korfi, Koorosh; Lechmann, Martin; Eigenmann, Miro Julian; Marbach, Daniel; Jamois, Candice; Lechner, Katharina; Krishnan, Sreenath M; Gaillard, Brenda; Marinho, Joana; Kronenberg, Sven; Kunz, Leo; Wilson, Sabine; Briner, Stefanie; Gebhardt, Samuel; Varol, Ahmet; Appelt, Birte; Nicolini, Valeria; Speziale, Dario; Bez, Miriam; Bommer, Esther; Eckmann, Jan; Hage, Carina; Limani, Florian; Jenni, Silvia; Schoenle, Anne; Le Clech, Marine; Vallier, Jean-Baptiste Pierre; Colombetti, Sara; Bacac, Marina; Gasser, Stephan; Klein, Christian; Umaña, Pablo.
Afiliação
  • Sam J; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Hofer T; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Kuettel C; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Claus C; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Thom J; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Herter S; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Georges G; Roche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
  • Korfi K; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Lechmann M; Roche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
  • Eigenmann MJ; Roche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
  • Marbach D; Roche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
  • Jamois C; Roche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
  • Lechner K; Roche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
  • Krishnan SM; Roche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
  • Gaillard B; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Marinho J; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Kronenberg S; Roche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
  • Kunz L; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Wilson S; Roche Innovation Center Welwyn, Roche Pharma Research and Early Development, Welwyn Garden City, United Kingdom.
  • Briner S; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Gebhardt S; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Varol A; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Appelt B; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Nicolini V; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Speziale D; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Bez M; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Bommer E; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Eckmann J; Roche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
  • Hage C; Roche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
  • Limani F; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Jenni S; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Schoenle A; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Le Clech M; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Vallier JP; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Colombetti S; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Bacac M; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Gasser S; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Klein C; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
  • Umaña P; Roche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Blood ; 143(21): 2152-2165, 2024 May 23.
Article em En | MEDLINE | ID: mdl-38437725
ABSTRACT
ABSTRACT Effective T-cell responses not only require the engagement of T-cell receptors (TCRs; "signal 1"), but also the availability of costimulatory signals ("signal 2"). T-cell bispecific antibodies (TCBs) deliver a robust signal 1 by engaging the TCR signaling component CD3ε, while simultaneously binding to tumor antigens. The CD20-TCB glofitamab redirects T cells to CD20-expressing malignant B cells. Although glofitamab exhibits strong single-agent efficacy, adding costimulatory signaling may enhance the depth and durability of T-cell-mediated tumor cell killing. We developed a bispecific CD19-targeted CD28 agonist (CD19-CD28), RG6333, to enhance the efficacy of glofitamab and similar TCBs by delivering signal 2 to tumor-infiltrating T cells. CD19-CD28 distinguishes itself from the superagonistic antibody TGN1412, because its activity requires the simultaneous presence of a TCR signal and CD19 target binding. This is achieved through its engineered format incorporating a mutated Fc region with abolished FcγR and C1q binding, CD28 monovalency, and a moderate CD28 binding affinity. In combination with glofitamab, CD19-CD28 strongly increased T-cell effector functions in ex vivo assays using peripheral blood mononuclear cells and spleen samples derived from patients with lymphoma and enhanced glofitamab-mediated regression of aggressive lymphomas in humanized mice. Notably, the triple combination of glofitamab with CD19-CD28 with the costimulatory 4-1BB agonist, CD19-4-1BBL, offered substantially improved long-term tumor control over glofitamab monotherapy and respective duplet combinations. Our findings highlight CD19-CD28 as a safe and highly efficacious off-the-shelf combination partner for glofitamab, similar TCBs, and other costimulatory agonists. CD19-CD28 is currently in a phase 1 clinical trial in combination with glofitamab. This trial was registered at www.clinicaltrials.gov as #NCT05219513.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos CD28 / Anticorpos Biespecíficos / Antígenos CD20 / Antígenos CD19 / Imunoterapia Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antígenos CD28 / Anticorpos Biespecíficos / Antígenos CD20 / Antígenos CD19 / Imunoterapia Idioma: En Ano de publicação: 2024 Tipo de documento: Article