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Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics

BACKGROUND: Orthopedia homeobox (OTP) has shown to be a useful prognostic marker to predict outcome in pulmonary carcinoids, which is also supported by the World Health Organization. However, the discontinuation of the initially used polyclonal antibody and absence of a reliable routinely applicable...

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Autores principales: Moonen, Laura, Derks, Jules L., Lap, Lisa M. V., Marijnissen, Britney J. C. A., Hillen, Lisa M., den Bakker, Michael A., von der Thüsen, Jan H., van Suylen, Robert-Jan, Timens, Wim, Bintanel, Maria, Kuteeva, Eugenia, Dingemans, Anne-Marie C., Speel, Ernst-Jan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742615/
https://www.ncbi.nlm.nih.gov/pubmed/36519022
http://dx.doi.org/10.21037/tlcr-22-418
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author Moonen, Laura
Derks, Jules L.
Lap, Lisa M. V.
Marijnissen, Britney J. C. A.
Hillen, Lisa M.
den Bakker, Michael A.
von der Thüsen, Jan H.
van Suylen, Robert-Jan
Timens, Wim
Bintanel, Maria
Kuteeva, Eugenia
Dingemans, Anne-Marie C.
Speel, Ernst-Jan M.
author_facet Moonen, Laura
Derks, Jules L.
Lap, Lisa M. V.
Marijnissen, Britney J. C. A.
Hillen, Lisa M.
den Bakker, Michael A.
von der Thüsen, Jan H.
van Suylen, Robert-Jan
Timens, Wim
Bintanel, Maria
Kuteeva, Eugenia
Dingemans, Anne-Marie C.
Speel, Ernst-Jan M.
author_sort Moonen, Laura
collection PubMed
description BACKGROUND: Orthopedia homeobox (OTP) has shown to be a useful prognostic marker to predict outcome in pulmonary carcinoids, which is also supported by the World Health Organization. However, the discontinuation of the initially used polyclonal antibody and absence of a reliable routinely applicable monoclonal OTP antibody hampers implementation in routine diagnostics. Here, new monoclonal antibodies directed against OTP were developed and verified on formalin-fixed paraffin-embedded tissue of pulmonary neuroendocrine tumors (NETs) for clinical diagnostics. METHODS: OTP specific monoclonal antibodies were produced from mice immunised with a recombinant human OTP protein fragment. Enzyme-linked immunosorbent assay (ELISA) positive hybridomas were evaluated using immunohistochemistry (IHC). Following epitope-mapping and isotyping, purified monoclonal antibodies were validated for IHC in formalin-fixed paraffin-embedded tissues, the optimal dilution was determined, and results were cross validated with the OTP polyclonal antibody (HPA039365, Atlas Antibodies). Staining protocols were optimized on two automated staining platforms and performance was harmonized using a tissue microarray (TMA). RESULTS: Two clones (CL11222 and CL11225) were selected for purified monoclonal antibody (mAb) production. Intratumor heterogeneity assessment revealed similar performance for both clones. While clone CL11225 displayed a unique epitope compared to those present in the polyclonal antibody, this clone performed most similar to the polyclonal antibody. Cross-platform assessment revealed an excellent agreement for clone CL11225 while clone CL11222 showed somewhat discordant results on Dako. CONCLUSIONS: New monoclonal OTP specific antibodies have been developed and verified on different automated immunohistochemical staining platforms. The OTP specific monoclonal antibodies showed excellent agreement with the often-used polyclonal antibody allowing application in routine diagnostics.
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spelling pubmed-97426152022-12-13 Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics Moonen, Laura Derks, Jules L. Lap, Lisa M. V. Marijnissen, Britney J. C. A. Hillen, Lisa M. den Bakker, Michael A. von der Thüsen, Jan H. van Suylen, Robert-Jan Timens, Wim Bintanel, Maria Kuteeva, Eugenia Dingemans, Anne-Marie C. Speel, Ernst-Jan M. Transl Lung Cancer Res Original Article BACKGROUND: Orthopedia homeobox (OTP) has shown to be a useful prognostic marker to predict outcome in pulmonary carcinoids, which is also supported by the World Health Organization. However, the discontinuation of the initially used polyclonal antibody and absence of a reliable routinely applicable monoclonal OTP antibody hampers implementation in routine diagnostics. Here, new monoclonal antibodies directed against OTP were developed and verified on formalin-fixed paraffin-embedded tissue of pulmonary neuroendocrine tumors (NETs) for clinical diagnostics. METHODS: OTP specific monoclonal antibodies were produced from mice immunised with a recombinant human OTP protein fragment. Enzyme-linked immunosorbent assay (ELISA) positive hybridomas were evaluated using immunohistochemistry (IHC). Following epitope-mapping and isotyping, purified monoclonal antibodies were validated for IHC in formalin-fixed paraffin-embedded tissues, the optimal dilution was determined, and results were cross validated with the OTP polyclonal antibody (HPA039365, Atlas Antibodies). Staining protocols were optimized on two automated staining platforms and performance was harmonized using a tissue microarray (TMA). RESULTS: Two clones (CL11222 and CL11225) were selected for purified monoclonal antibody (mAb) production. Intratumor heterogeneity assessment revealed similar performance for both clones. While clone CL11225 displayed a unique epitope compared to those present in the polyclonal antibody, this clone performed most similar to the polyclonal antibody. Cross-platform assessment revealed an excellent agreement for clone CL11225 while clone CL11222 showed somewhat discordant results on Dako. CONCLUSIONS: New monoclonal OTP specific antibodies have been developed and verified on different automated immunohistochemical staining platforms. The OTP specific monoclonal antibodies showed excellent agreement with the often-used polyclonal antibody allowing application in routine diagnostics. AME Publishing Company 2022-11 /pmc/articles/PMC9742615/ /pubmed/36519022 http://dx.doi.org/10.21037/tlcr-22-418 Text en 2022 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Moonen, Laura
Derks, Jules L.
Lap, Lisa M. V.
Marijnissen, Britney J. C. A.
Hillen, Lisa M.
den Bakker, Michael A.
von der Thüsen, Jan H.
van Suylen, Robert-Jan
Timens, Wim
Bintanel, Maria
Kuteeva, Eugenia
Dingemans, Anne-Marie C.
Speel, Ernst-Jan M.
Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics
title Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics
title_full Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics
title_fullStr Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics
title_full_unstemmed Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics
title_short Development and verification of new monoclonal orthopedia homeobox (OTP) specific antibodies for pulmonary carcinoid diagnostics
title_sort development and verification of new monoclonal orthopedia homeobox (otp) specific antibodies for pulmonary carcinoid diagnostics
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742615/
https://www.ncbi.nlm.nih.gov/pubmed/36519022
http://dx.doi.org/10.21037/tlcr-22-418
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