Journal
BRITISH JOURNAL OF CANCER
Volume 120, Issue 3, Pages 317-330Publisher
SPRINGERNATURE
DOI: 10.1038/s41416-018-0352-y
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Funding
- National Natural Science Foundation of China [81472516]
- Natural Science Foundation of Shanghai [14ZR1424200]
- China Postdoctoral Science Foundation [2018M632141]
- Shanghai Leading Academic Discipline Project [S30206]
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BACKGROUND: An immunosuppressive microenvironment is critical for cancer initiation and progression. Whether interferon alpha (IFN alpha) can suppress immune and cancer cells and its involved mechanism still remain largely elusive. METHODS: We examine the expression of interferon alpha/beta receptor-1 (IFNAR1), CD8, CD56 and programmed death ligand 1 (PDL1) in head and neck squamous cell carcinomas (HNSCC). The effect of IFNa on PDL1 and programmed cell death protein 1 (PD1) expression in tumour cells and immune cells was detected in vitro and in vivo. RESULTS: Overexpression of IFNAR1, MX1 and signal transducer and activator of transcription 1 (Stat1) indicated the endogenous IFNa activation in tumour microenvironment, which correlated with immunosuppression status in HNSCC patients. Moreover, IFNa transcriptionally activated the expression of PDL1 through p-Stat1 (Tyr701) and promoted PD1 expression in immune cells through IFNAR1. The inhibition of IFNa signalling enhanced the cytotoxic activity of nature killer cells. At lastastly, we confirmed the upregulation of PDL1 and PD1 in response to IFNa treatment in both xenograft tumour models and patient-derived xenograft models. CONCLUSIONS: Our findings demonstrate that IFN alpha-induced PDL1 and PD1 expression is a new mechanism of immunosuppression in HNSCC, suggesting that blocking IFNa signalling may enhance the efficacy of immune checkpoint blockade.
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