Programmed death-ligand 1 and its soluble form are highly expressed in nasal natural killer/T-cell lymphoma: a potential rationale for immunotherapy
- Toshihiro Nagato(corresponding author),
- Takayuki Ohkuri,
- Kenzo Ohara,
- Yui Hirata,
- Kan Kishibe,
- Yuki Komabayashi
- Asahikawa Medical University,
Open access
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
Nasal natural killer/T-cell lymphoma (NNKTL) is an aggressive neoplasm with poor therapeutic responses and prognosis. The programmed death-1/programmed death-ligand 1 (PD-1/PD-L1) pathway plays an important role in immune evasion of tumor cells through T-cell exhaustion. The aim of the present study was to examine the expression of PD-L1 and PD-1 molecules in NNKTL. We detected the expression of PD-L1 in biopsy samples from all of the NNKTL patients studied. PD-L1 was found on both malignant cells and tumor-infiltrating macrophages, while PD-1-positive mononuclear cells infiltrated the tumor tissues in 36% of patients. Most significantly, soluble PD-L1 (sPD-L1) was present in sera of NNKTL patients at higher levels as compared to healthy individuals and the levels of serum sPD-L1 in patients positively correlated with the expression of PD-L1 in lymphoma cells of tumor tissues. In addition, the high-sPD-L1 group of patients showed significantly worse prognosis than the low-sPD-L1 group. Furthermore, we confirmed that membrane and soluble PD-L1 was expressed on the surface and in the culture supernatant, respectively, of NNKTL cell lines. The expression of PD-L1 was observed in tumor tissues and sera from a murine xenograft model inoculated with an NNKTL cell line. Our results suggest that sPD-L1 could be a prognostic predictor for NNKTL and open up the possibility of immunotherapy of this lymphoma using PD-1/PD-L1 axis inhibitors.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 877-890 (14 pages)Journal (Volume, Issue Number)
Cancer Immunology, Immunotherapy (Volume 66, Issue 7)Publication milestones
- Accepted/In press - 03/27/2017
- Published - 07/01/2017
Publication status
ISSN
0340-7004Publication IDs
- Scopus: 85016094553
- PubMed: 28349165
