| Literature DB >> 31327656 |
Heng-Huan Lee1, Ying-Nai Wang1, Weiya Xia1, Chia-Hung Chen2, Kun-Ming Rau3, Leiguang Ye4, Yongkun Wei1, Chao-Kai Chou1, Shao-Chun Wang5, Meisi Yan6, Chih-Yen Tu2, Te-Chun Hsia2, Shu-Fen Chiang7, K S Clifford Chao7, Ignacio I Wistuba8, Jennifer L Hsu9, Gabriel N Hortobagyi10, Mien-Chie Hung11.
Abstract
Reactivation of T cell immunity by PD-1/PD-L1 immune checkpoint blockade has been shown to be a promising cancer therapeutic strategy. However, PD-L1 immunohistochemical readout is inconsistent with patient response, which presents a clinical challenge to stratify patients. Because PD-L1 is heavily glycosylated, we developed a method to resolve this by removing the glycan moieties from cell surface antigens via enzymatic digestion, a process termed sample deglycosylation. Notably, deglycosylation significantly improves anti-PD-L1 antibody binding affinity and signal intensity, resulting in more accurate PD-L1 quantification and prediction of clinical outcome. This proposed method of PD-L1 antigen retrieval may provide a practical and timely approach to reduce false-negative patient stratification for guiding anti-PD-1/PD-L1 therapy.Entities:
Keywords: PD-1; PD-L1; antibody-based detection; biomarker; glycosylation/deglycosylation; heterogeneity/homogeneity; immune checkpoint; immunohistochemistry; immunotherapy
Year: 2019 PMID: 31327656 PMCID: PMC6793936 DOI: 10.1016/j.ccell.2019.06.008
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743