4.5 Article

Modulation of tumor immunity: a patent evaluation of WO2015026684A1

Journal

EXPERT OPINION ON THERAPEUTIC PATENTS
Volume 26, Issue 3, Pages 417-425

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/13543776.2016.1118061

Keywords

TILs (tumor-infiltrating lymphocytes); Immune checkpoint treatment; Tregs (regulatory T cells); combination treatment; GITR (glucocorticoid-induced TNF receptor-related molecule); PD-1 (programmed cell death 1); co-accessory molecules; solid tumors

Funding

  1. Ministero dell'Istruzione dell'Universita e della Ricerca (MIUR) [2008SKTMME_003]
  2. MIUR [2006052432_001]
  3. Associazione Italiana per la Ricerca contro il Cancro (AIRC) [IG-10677, IG-14291]
  4. AIRC [IG-14291]

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A high percentage of regulatory T cells (Tregs) among tumor-infiltrating lymphocytes weakens the immune response against tumors. The anergy of effector T cells (Teff) can be reversed by immune checkpoint treatment, which inhibits Tregs and boosts the activation of Teff. Both effects can be obtained by triggering the glucocorticoid-induced TNF receptor-related (GITR), a costimulatory molecule expressed by Teff and Tregs, and by inhibiting the programmed cell death (PD)-1 receptor, an inhibitory molecule expressed by Teff. Patent W02015026684A1 provides a method of treating human tumors using a combination of a molecule triggering GITR and another inhibiting PD-1. The treatment approach was tested on three murine models of cancer, and the synergic effect of antihuman antibodies (Abs) in combination was tested in mixed lymphocyte reactions. Immune checkpoint treatment can break tolerance toward tumors and promote tumor rejection. The patented approach is very interesting and might be successful. The combined use of PD-1 antagonists and GITR agonists is synergic and tumor-centered, and adverse events might be less problematic than expected. A crucial point in translating the murine studies to humans is the differences between murine and human GITR and the evidence that some antihuman GITR Abs are not agonists.

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