IgE is ideally suited to treat solid tumours

T cell infiltration into tumour after treatment with a therapeutic IgE

Unique and multifaceted mechanism of action

  • Tumour antigen-specific IgE binds very tightly to FcεRI receptor on surface of myeloid cells such as macrophages
  • Facilitates tissue immunosurveillance by IgE-activated macrophages
  • IgE-activated macrophages permeate tumour and release pro-inflammatory mediators
  • Attracts and activates CD4+ and CD8+ T cells which destroy the tumour

Allows combinations with other modalities

  • IgE has demonstrated strong single agent activity in vivo in a variety of settings
  • Unique MoA allows combination with other modalities such as CPIs and ADCs
  • IgE successfully combines in vivo with CPIs in HER2-low breast cancer model

Potent activity in ultra-low antigen cancers

  • IgE has potent activity against tumour cells expressing ultra-low levels of FR⍺ and HER2
  • In vivo Proof of Concept in triple-negative breast cancer achieved
  • MOv18 IgE has demonstrated clinical activity in patients with low FR⍺

IgE Lights the Macrophage Fuse which Detonates the T Cell Bomb

 

  • IgE causes tumour antigen-specific macrophage permeation
    of tumour
  • Pro-inflammatory cytokines and chemokines released
  • Cytokines attract and activate T cells inside tumour
  • T cells destroy tumour
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