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PD-L2 based immune signature confers poor prognosis in HNSCC

PD-L2 expression is an important predictor of anti-PD-1 therapy efficacy in patients with head and neck squamous cell carcinoma (HNSCC). However, whether the PD-L2-based immune signature can serve as a prognostic biomarker for patients with HNSCC remains unclear. Here, we reported that PD-L2 was pos...

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Detalles Bibliográficos
Autores principales: Qiao, Yu, Liu, Chao, Zhang, Xiaoyue, Zhou, Qianqian, Li, Yatian, Xu, Yini, Gao, Zhenyue, Xu, Yiqi, Kong, Lingping, Yang, Aifeng, Mei, Mei, Ren, Yu, Wang, Xudong, Zhou, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344752/
https://www.ncbi.nlm.nih.gov/pubmed/34377590
http://dx.doi.org/10.1080/2162402X.2021.1947569
Descripción
Sumario:PD-L2 expression is an important predictor of anti-PD-1 therapy efficacy in patients with head and neck squamous cell carcinoma (HNSCC). However, whether the PD-L2-based immune signature can serve as a prognostic biomarker for patients with HNSCC remains unclear. Here, we reported that PD-L2 was positively stained in 62.7% of tumors, which was more than twice as that of PD-L1, and in 61.4% of patients with PD-L1-negative tumors. Survival tree analysis (STA) revealed that PD-L2(high) was an independent predictor of poor overall survival (OS). Six patterns were generated from STA, demonstrating that patients with PD-L2(low)CD3(high) were associated with an improved median OS of 72 months and prognostic index (PI) of −3.95 (95% CI, −5.14 to −2.76), whereas patients with PD-L2(high)CD3(low)CD8(low) to a median OS of 10 months and PI of 1.43 (95% CI, 0.56 to 2.30). Analysis of single-cell RNA sequencing showed that PD-L2 expression was associated with IL-6 expression. We confirmed that IL-6 augments PD-L2 expression in HNSCC cell lines. The PD-L2-based immune signature can serve as an effective biomarker for anti-PD-1 therapy. In addition, PD-L2 may serve as a potential immunotherapeutic target, and we propose anti-IL6 therapy in the adjuvant setting for patients with HNSCC with high PD-L2 expression.