4.6 Article

Infiltration of PD-1-positive cells in combination with tumor site PD-L1 expression is a positive prognostic factor in cutaneous angiosarcoma

期刊

ONCOIMMUNOLOGY
卷 6, 期 1, 页码 -

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/2162402X.2016.1253657

关键词

Cutaneous angiosarcoma; IFN gamma; PD-1; PD-L1; T cells

资金

  1. Japan Society for the Promotion of Science [15H05790, 15H1155, 15K15417]
  2. Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology (PRESTO) [16021031300]
  3. Japan Agency for Medical Research and Development (AMED) [16ek0410011h0003, 16he0902003h0002]
  4. Grants-in-Aid for Scientific Research [15K15417, 15K08362, 15H05790] Funding Source: KAKEN

向作者/读者索取更多资源

Cutaneous angiosarcoma (CAS) is a malignant sarcoma with poor prognosis. Programmed cell death-1 (PD-1)/programmed cell death-1 ligand-1 (PD-L1) expression reflects antitumor immunity, and is associated with patient prognosis in various cancers. The purpose of this study is to investigate the relationship between PD-1/PD-L1 expression and CAS prognosis. CAS cases (n D 106) were immunohistochemically studied for PD-L1 and PD-1 expression, and the correlation with patient prognosis was analyzed. PD-L1 expression was assessed by flow cytometry on three CAS cell lines with or without IFNg stimulation. A total of 30.2% of patients' samples were positive for PD-L1, and 17.9% showed a high infiltration of PD-1-positive cells. Univariate analysis showed a significant relationship between a high infiltration of PD-1-positive cells with tumor site PD-L1 expression and favorable survival in stage 1 patients (p D 0.014, log-rank test). Multivariable Cox-proportional hazard regression analysis also showed that patients with a high infiltration of PD-1-positive cells with tumor site PD-L1 expression were more likely to have favorable survival, after adjustment with possible confounders (hazard ratio (HR) D 0.38, p D 0.021, 95% confidence interval (CI) 0.16-0.86). Immunofluorescence staining of CAS samples revealed that PD-L1-positive cells were adjacent to PD-1-positive cells and/or tumor stroma with high IFN gamma expression. In vitro stimulation with IFN gamma increased PD-L1 expression in two out of three established CAS cell lines. Our results suggest that PD-1/PD-L1 expression is related to CAS progression, and the treatment with antiPD-1 antibodies could be a new therapeutic option for CAS.

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