Abstract
<div>Abstract<p><b>Purpose:</b> Carcinoembryonic antigen (CEA) is a candidate target for cellular immunotherapy of pancreatic cancer. In this study, we have characterized the antigen-specific function of autologous cytotoxic T lymphocytes (CTL) specific for the HLA-A2–restricted peptide, pCEA691-699, isolated from the peripheral T-cell repertoire of pancreatic cancer patients and sought to determine if <i>ex vivo</i> PD-L1 and TIM-3 blockade could enhance CTL function.</p><p><b>Experimental Design:</b> CD8<sup>+</sup> T-cell lines were generated from peripheral blood mononuclear cells of 18 HLA-A2<sup>+</sup> patients with pancreatic cancer and from 15 healthy controls. <i>In vitro</i> peptide-specific responses were evaluated by flow cytometry after staining for intracellular cytokine production and carboxy fluorescein succinimydyl ester cytotoxicity assays using pancreatic cancer cell lines as targets.</p><p><b>Results:</b> Cytokine-secreting functional CEA691-specific CTL lines were successfully generated from 10 of 18 pancreatic cancer patients, with two CTL lines able to recognize and kill both CEA691 peptide–loaded T2 cells and CEA<sup>+</sup> HLA-A2<sup>+</sup> pancreatic cancer cell lines. In the presence of <i>ex vivo</i> PD-L1 blockade, functional CEA691-specific CD8<sup>+</sup> T-cell responses, including IFNγ secretion and proliferation, were enhanced, and this effect was more pronounced on Ag-specific T cells isolated from tumor draining lymph nodes.</p><p><b>Conclusions:</b> These data demonstrate that CEA691-specific CTL can be readily expanded from the self-restricted T-cell repertoire of pancreatic cancer patients and that their function can be enhanced by PD-L1 blockade. <i>Clin Cancer Res; 23(20); 6178–89. ©2017 AACR</i>.</p></div>
Published Version
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