American Association for Cancer Research
00085472can124460-sup-can-12-4460_matmet_figs_1_3.pdf (113.21 kB)

Supplementary Materials and Methods and Figures 1-3 from Potent Immunomodulatory Effects of the Trifunctional Antibody Catumaxomab

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journal contribution
posted on 2023-03-30, 21:55 authored by Diane Goéré, Caroline Flament, Sylvie Rusakiewicz, Vichnou Poirier-Colame, Oliver Kepp, Isabelle Martins, Julien Pesquet, Alexander Eggermont, Dominique Elias, Nathalie Chaput, Laurence Zitvogel

PDF - 115K, upplemental Figure 1. Activation of CD4+ T cells by CatmAb in mixed lymphocyte tumor cocultures. Supplemental Figure 2. Activation of CD8+ T cells by CatmAb in mixed lymphocyte tumor cocultures. Supplemental Figure 3. Activation of NK cells by CatmAb in mixed lymphocyte tumor cocultures.



Catumaxomab (CatmAb), a trifunctional bispecific antibody directed against the epithelial cell adhesion molecule (EpCAM) and the T-cell antigen CD3, is approved as intraperitoneal therapy for the treatment of malignant ascites in patients with EpCAM-positive carcinomas. The immunomonitoring results of a phase II/III study using CatmAb revealed a tumoricidal effect associated with reduced VEGF levels, CD69-expressing T cells, and the release of T-helper cell (TH)-1 cytokines. We comprehensively dissected the immunomodulatory effects of the CatmAb on the major subsets of malignant ascites-infiltrating leukocytes and the molecular fingerprint of tumor cell death. Herein we show that in the presence of EpCAM-positive tumor targets, CatmAb markedly enhanced T-cell activation [CD69, CD107A (LAMP1), HLA-DR and PD-1(PDCD1) expression] and stimulated inflammatory CD4+ TH1 and CD8+ TH1 to release IFN-γ but failed to trigger TH17 cells. Engagement of CD16-expressing cells caused upregulation of TRAIL (TNFSF10) and costimulatory CD40 and CD80 molecules. CatmAb promoted tumor cell death associated with ATP release and strongly synergized with oxaliplatin for the exposure of the three hallmarks of immunogenic cell death (calreticulin, HMGB1, and ATP). These findings warrant validation as potential biomarkers of efficacy of CatmAb. Cancer Res; 73(15); 4663–73. ©2013 AACR.

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