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P06.04 Immune responses against shared antigens are common in esophago-gastric cancer and can be enhanced using CD40-activated B cells
  1. M Thelen1,
  2. D Keller1,
  3. J Lehmann1,
  4. K Wennhold1,
  5. H Weitz1,
  6. E Bauer1,
  7. B Gathof1,
  8. M Brüggemann2,
  9. M Kotrova2,
  10. A Quaas1,
  11. C Mallmann1,
  12. S Chon1,
  13. AM Hillmer1,
  14. C Bruns1,
  15. M von Bergwelt-Baildon3,
  16. MA Garcia-Marquez1 and
  17. HA Schlößer1
  1. 1University of Cologne, Cologne, Germany
  2. 2Universitätsklinikum Schleswig-Holstein, Kiel, Germany
  3. 3Ludwig Maximilians University, Munich, Germany


Background Specific immune response is a hallmark of cancer immunotherapy and shared tumor-associated antigens (TAAs) are important targets. Recent advances using combined cellular therapy against multiple TAAs renewed the interest in this class of antigens. Our study aims to determine the role of TAAs in esophago-gastric adenocarcinoma (EGA).

Materials and Methods RNA expression was assessed by NanoString in tumor samples of 41 treatment-naïve EGA patients. Endogenous T cell and antibody responses against the 10 most relevant TAAs were determined by FluoroSpot and protein-bound bead assays. Digital image analysis was used to evaluate the correlation of TAAs and T-cell abundance. T-cell receptor sequencing, in-vitro expansion with autologous CD40-activated B cells (CD40Bs) and in-vitro cytotoxicity assays were applied to determine specific expansion, clonality and cytotoxic activity of expanded T cells.

Results 68.3% of patients expressed ≥5 TAAs simultaneously with co-regulated clusters, which were similar to data from The Cancer Genome Atlas (n=505). Endogenous cellular or humoral responses against ≥1 TAA were detectable in 75.0% and 53.7% of patients, respectively. We found a correlation of T-cell abundance and the expression of TAAs and genes related to antigen-presentation. TAA-specific T-cell responses were polyclonal, could be induced or enhanced using autologous CD40Bs and were cytotoxic in-vitro. Despite the frequent expression of TAAs co-occurrence with immune responses was rare.

Conclusions We identified the most relevant TAAs in EGA for monitoring of clinical trials and as therapeutic targets. Antigen-escape rather than missing immune response should be considered as mechanism underlying immunotherapy resistance of EGA.

Disclosure Information M. Thelen: None. D. Keller: None. J. Lehmann: None. K. Wennhold: None. H. Weitz: None. E. Bauer: None. B. Gathof: None. M. Brüggemann: None. M. Kotrova: None. A. Quaas: None. C. Mallmann: None. S. Chon: None. A.M. Hillmer: None. C. Bruns: None. M. von Bergwelt-Baildon: B. Research Grant (principal investigator, collaborator or consultant and pending grants as well as grants already received); Modest; Astellas, Roche, SD. F. Consultant/Advisory Board; Modest; Bristol Myers Squibb. M.A. Garcia-Marquez: None. H.A. Schlößer: B. Research Grant (principal investigator, collaborator or consultant and pending grants as well as grants already received); Modest; Astra Zeneca.

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