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PD-1+ Tim3+ tumor-infiltrating CD8 T cells sustain the potential for IFN-γ production, but lose cytotoxic activity in ovarian cancer.

Abstract
Persistent exposure to tumor antigens results in exhausted tumor-infiltrating T cells (TILs) that express the immune checkpoint molecules, PD-1 and Tim3, and lack anti-tumor immunity. To examine the exhausted status of TILs in ovarian cancer, the potential for cytokine production, proliferation and cytotoxicity by purified PD-1+ Tim3+ CD8 TILs was assessed. The production of IFN-γ and TNF-α by PD-1+ Tim3+ CD8 TILs remained the same in an intracellular cytokine staining assay and was higher in a cytokine catch assay than that by PD-1- Tim3- and PD-1+ Tim3- CD8 TILs. %Ki67+ was higher in PD-1+ Tim3+ CD8 TILs than in PD-1- Tim3- CD8 TILs. However, patients with high PD-1+ Tim3+ CD8 TILs had a poor prognosis. The potential for cytotoxicity was then examined. %Perforin+ and %granzyme B+ were lower in PD-1+ Tim3+ CD8 TILs than in PD-1- Tim3- and PD-1+ Tim3- CD8 TILs. To observe the potential for direct cytotoxicity by T cells, a target cell line expressing membrane-bound anti-CD3scFv was newly established and a cytotoxic assay targeting these cells was performed. The cytotoxicity of PD-1+ Tim3+ CD8 TILs was significantly lower than that of PD-1- Tim3- and PD-1+ Tim3- CD8 TILs. Even though PD-1+ Tim3+ CD8 TILs in ovarian cancer showed a sustained potential for cytokine production and proliferation, cytotoxicity was markedly impaired, which may contribute to the poor prognosis of patients with ovarian cancer. Among the impaired functions of exhausted TILs, cytotoxicity may be an essential target for cancer immunotherapy.
AuthorsMasaaki Sawada, Kumiko Goto, Akiko Morimoto-Okazawa, Miya Haruna, Kei Yamamoto, Yoko Yamamoto, Satoshi Nakagawa, Kosuke Hiramatsu, Shinya Matsuzaki, Eiji Kobayashi, Atsunari Kawashima, Michinari Hirata, Kota Iwahori, Toshihiro Kimura, Yutaka Ueda, Tadashi Kimura, Hisashi Wada
JournalInternational immunology (Int Immunol) Vol. 32 Issue 6 Pg. 397-405 (05 30 2020) ISSN: 1460-2377 [Electronic] England
PMID32009163 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© The Japanese Society for Immunology. 2020. All rights reserved. For permissions, please e-mail: [email protected].
Chemical References
  • HAVCR2 protein, human
  • Hepatitis A Virus Cellular Receptor 2
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Interferon-gamma
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • CD8-Positive T-Lymphocytes (immunology)
  • Cell Proliferation
  • Female
  • Hepatitis A Virus Cellular Receptor 2 (deficiency, immunology)
  • Humans
  • Immunotherapy
  • Interferon-gamma (biosynthesis, immunology)
  • Lymphocytes, Tumor-Infiltrating (immunology)
  • Middle Aged
  • Ovarian Neoplasms (diagnosis, immunology, metabolism, therapy)
  • Programmed Cell Death 1 Receptor (deficiency, immunology)

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