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Updated: Jan 22, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Programmed death ligand 1 (PD-L1) expression in parathyroid tumors
Boju Pan1, Anqi Wang2, Junyi Pang1
1Department of Pathology, Molecular Pathology Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Programmed death-ligand 1 (PD-L1) expression is largely deficient in parathyroid tumors. PD-L1 scoring in these tumors varies significantly based on the antibody clone used for assessment.
Area of Science:
- Oncology
- Endocrinology
- Immunology
Background:
- Programmed death-ligand 1 (PD-L1) is a key immune checkpoint molecule implicated in cancer prognosis and response to immunotherapy.
- Previous research has identified PD-L1 expression in various endocrine tumors, but its status in parathyroid neoplasms remained uncharacterized.
Purpose of the Study:
- To investigate the expression of PD-L1 in parathyroid carcinoma and adenoma.
- To evaluate the consistency of PD-L1 detection using different antibody clones.
Main Methods:
- Analysis of 26 parathyroid carcinoma and 37 adenoma samples.
- Immunohistochemical staining for PD-L1 using FDA-approved 22C3 and SP263 assays.
- Assessment of PD-L1 expression in tumor cells and tumor-infiltrating immune cells, correlated with Ki-67 index and mitotic rate.
Main Results:
- A majority of parathyroid tumors exhibited deficient PD-L1 expression across both tumor cell and immune cell compartments.
- PD-L1 expression levels varied significantly between the SP263 and 22C3 antibody clones.
- A negative correlation was observed between PD-L1 expression and tumor proliferation markers (Ki-67, mitotic rate), with clone-dependent variations.
Conclusions:
- Parathyroid tumors generally show low PD-L1 expression.
- The choice of antibody clone significantly impacts PD-L1 scoring in parathyroid neoplasms.
- Further investigation is warranted to standardize PD-L1 assessment in this tumor type.
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