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Decreased invariant natural killer T‐cell‐mediated antitumor immune response in patients with gastric cancer
Author(s) -
Ascui Gabriel,
GálvezJirón Felipe,
Kramm Karina,
Schäfer Carolina,
Siña Josefina,
Pola Víctor,
Cristi Francisca,
Hernández Carolina,
GarridoTapia Macarena,
Pesce Bárbara,
Bustamante Marco,
Fluxá Paula,
Molina María C,
Ribeiro Carolina H
Publication year - 2020
Publication title -
immunology and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.999
H-Index - 104
eISSN - 1440-1711
pISSN - 0818-9641
DOI - 10.1111/imcb.12331
Subject(s) - nkg2d , cd1d , immunology , immune system , natural killer t cell , biology , cancer research , cytotoxic t cell , t cell , in vitro , biochemistry
Gastric cancer (GC) is the third most common cause of cancer‐related death worldwide. Invariant natural killer T (iNKT) cells are innate‐like cytotoxic T lymphocytes involved in tumor immune surveillance. They can be activated either through CD1d‐presented glycolipid antigens recognized by their invariant T‐cell receptor, cytokines or by sensing tumor‐associated stress‐induced ligands through the natural killer group 2, member D (NKG2D) receptor. Although the number and functionality of iNKT cells may be decreased in several types of cancer, here we show that GC patients presented a mild increase in iNKT cell frequencies and numbers in the blood compared with healthy donors. In GC patients, iNKT cells, expanded in vitro with α‐galactosyl ceramide and stimulated with phorbol 12‐myristate 13‐acetate and ionomycin, produced higher levels of interleukin‐2 and transforming growth factor‐beta, while their capacity to degranulate remained preserved. Because tumor‐derived epithelial cell adhesion molecule‐positive epithelial cells did not display surface CD1d, and NKG2D ligands (NKG2DLs) were detected in the gastric tumor milieu, we envisioned a role for NKG2D in iNKT cell functions. Peripheral iNKT cells from GC patients and controls presented similar levels of NKG2D; nevertheless, the percentages of interferon‐γ‐producing and CD107a‐positive iNKT cells from patients were reduced upon challenge with CD1d‐negative, NKG2DL‐positive K562 cells, suggesting a compromised response by iNKT cells in GC patients, which may not result from impaired NKG2D/NKG2DL signaling. The decreased response of iNKT cells may explain the fact that higher frequencies of circulating iNKT cells did not confer a survival benefit for GC patients. Therefore, functional impairment of iNKT cells in GC may contribute to tumor immune escape and favor disease progression.