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An Analytical Comparison of Dako 28-8 PharmDx Assay and an E1L3N Laboratory-Developed Test in the Immunohistochemical Detection of Programmed Death-Ligand 1.
- Source :
-
Molecular diagnosis & therapy [Mol Diagn Ther] 2017 Feb; Vol. 21 (1), pp. 85-93. - Publication Year :
- 2017
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Abstract
- Aim: Nivolumab, a fully human immunoglobulin G4 programmed death-1 (PD-1) immune checkpoint inhibitor antibody, has activity in melanoma, non-small-cell lung cancer (NSCLC), renal cell carcinoma (RCC), and Hodgkin lymphoma. Nivolumab is approved in the USA and EU for advanced melanoma, NSCLC, and RCC, and relapsed Hodgkin lymphoma in the USA. Programmed death-ligand 1 (PD-L1), a PD-1 ligand, is expressed on mononuclear leukocytes, myeloid cells, and tumor cells. PD-L1 is being investigated as a potential biomarker to predict the association of tumor PD-L1 expression with nivolumab efficacy.<br />Methods: Bristol-Myers Squibb and Dako previously reported on an automated PD-L1 immunohistochemical (IHC) assay that detects cell surface PD-L1 in formalin-fixed, paraffin-embedded, human tumor tissue specimens using Dako's Autostainer Link 48. The primary antibody for this assay is a rabbit monoclonal antihuman PD-L1 antibody, clone 28-8. Another rabbit monoclonal antihuman PD-L1 antibody, clone E1L3N, was compared with 28-8 for specificity and sensitivity using an identical detection method followed by vendor-recommended detection methods.<br />Results: Using PD-L1 null clones of L2987 and ES-2 tumor cell lines, both antibodies were specific for detection of PD-L1 on the plasma membrane, although E1L3N also stained cytoplasm in ES-2 knockout cells. Using the identical method, E1L3N was slightly more sensitive than 28-8 based on staining intensities. Using manufacturer-recommended detection methods and predefined scoring criteria for plasma membrane staining of tumor and immune cells, 28-8 demonstrated significantly improved detection compared with E1L3N.<br />Conclusions: Epitope retrieval and highly sensitive detection reagents are key determinants in IHC detection of PD-L1.<br />Competing Interests: Compliance with Ethical Standards Funding This work and open access publication were supported by funding from Bristol-Myers Squibb. Conflict of interest John Cogswell, H. David Inzunza, Qiuyan Wu, John Feder, Gabe Mintier, and James Novotny are employees of and stockholders in Bristol-Myers Squibb. Diana Cardona has served in a consulting or advisory role for Bristol-Myers Squibb.
- Subjects :
- Antibodies, Monoclonal chemistry
Antibodies, Monoclonal pharmacology
Antibody Specificity
Biomarkers, Tumor
Carcinoma, Non-Small-Cell Lung drug therapy
Carcinoma, Non-Small-Cell Lung metabolism
Cell Line, Tumor
Epitopes chemistry
Genetic Markers
Humans
Melanoma drug therapy
Melanoma metabolism
Nivolumab
Sensitivity and Specificity
B7-H1 Antigen isolation & purification
Immunohistochemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1179-2000
- Volume :
- 21
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Molecular diagnosis & therapy
- Publication Type :
- Academic Journal
- Accession number :
- 27667773
- Full Text :
- https://doi.org/10.1007/s40291-016-0237-9