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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
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    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

Scholary Output:
Contribution to journal
Article
Peer-review

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

Published - 07/01/2017

ISSN

0340-7004

Publication IDs

  • Scopus: 85016094553
  • PubMed: 28349165

Publication metrics

Metrics

Fractional count
1
Fractional count
0.05
Fractional count
19
Fractional count
0.95
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
4.88
SciVal
Author count
20
SciVal
citations
76
SciVal
Paper percentile
98
SciVal
Top percentile
5

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67
Citation count
150

Funding Details

The authors thank Dr. Norio Shimizu (Tokyo Medical and Dental University) for generously providing cell lines, Mr. Toshiyuki Hayakawa (Animal Laboratory for Medical Research, Center for Advanced Research and Education, Asahikawa Medical University) for devotedly maintaining mice, and Ms. Rie Matsumoto (Department of Pathology, Asahikawa Medical University) and Ms. Keiko Nishikura (Department of Dermatology, Asahikawa Medical University) for technical assistance. This study was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI [Grant Numbers 15K20172 (Nagato T), 26462576 (Kishibe K), 15H04986 (Harabuchi Y), and 16K15244 (Kobayashi H)].
FunderFunding numbers
KAKEN
15K20172, 15H04986, 16K15244, 15K20174, 26462576