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Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue
BACKGROUND: A T cell costimulatory molecule with dipeptidyl peptidase IV (DPPIV) activity in its extracellular region, CD26 is a multifunctional molecule associated with various proteins such as adenosine deaminase, caveolin-1, CXCR4, collagen, and fibronectin, while playing an important role in the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944398/ https://www.ncbi.nlm.nih.gov/pubmed/24502396 http://dx.doi.org/10.1186/1746-1596-9-30 |
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author | Hatano, Ryo Yamada, Taketo Matsuoka, Shuji Iwata, Satoshi Yamazaki, Hiroto Komiya, Eriko Okamoto, Toshihiro Dang, Nam H Ohnuma, Kei Morimoto, Chikao |
author_facet | Hatano, Ryo Yamada, Taketo Matsuoka, Shuji Iwata, Satoshi Yamazaki, Hiroto Komiya, Eriko Okamoto, Toshihiro Dang, Nam H Ohnuma, Kei Morimoto, Chikao |
author_sort | Hatano, Ryo |
collection | PubMed |
description | BACKGROUND: A T cell costimulatory molecule with dipeptidyl peptidase IV (DPPIV) activity in its extracellular region, CD26 is a multifunctional molecule associated with various proteins such as adenosine deaminase, caveolin-1, CXCR4, collagen, and fibronectin, while playing an important role in the regulation of inflammatory responses and tumor biology. We have focused on CD26 as a novel therapeutic target for various tumors and immune disorders, and have developed a humanized anti-CD26 monoclonal antibody (mAb), YS110, which is currently being evaluated in a phase I clinical trial for patients with CD26-expressing tumors, including malignant mesothelioma. Since detection of tumor CD26 expression is required for determining potential eligibility for YS110 therapy, the development of anti-human CD26 mAb that can clearly and reliably detect the denatured CD26 molecule in the formalin-fixed paraffin-embedded tissues is critical. METHODS: To develop novel anti-CD26 mAbs capable of binding to the denatured CD26, we immunized mice with CD26 protein denatured in urea buffer. After the fusion of splenocytes and myeloma cells, the mAbs were screened for specific reactivity with human CD26 by flow cytometry, enzyme-linked immunosorbent assay, and immunohistochemistry. The binding competitiveness of novel anti-CD26 mAbs with the humanized anti-CD26 mAb YS110 was also examined. RESULTS: We have succeeded in developing novel anti-human CD26 mAbs suitable for immunohistochemical staining of CD26 in formalin-fixed tissue sections with reliable clarity and intensity. Importantly, some of these mAbs exhibit no cross-reactivity with the humanized anti-CD26 mAb. CONCLUSIONS: These novel mAbs are potentially useful as companion diagnostic agents to analyze CD26 expression in the clinical setting while advancing future CD26-related research. VIRTUAL SLIDES: The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5987140221097729 |
format | Online Article Text |
id | pubmed-3944398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39443982014-03-07 Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue Hatano, Ryo Yamada, Taketo Matsuoka, Shuji Iwata, Satoshi Yamazaki, Hiroto Komiya, Eriko Okamoto, Toshihiro Dang, Nam H Ohnuma, Kei Morimoto, Chikao Diagn Pathol Research BACKGROUND: A T cell costimulatory molecule with dipeptidyl peptidase IV (DPPIV) activity in its extracellular region, CD26 is a multifunctional molecule associated with various proteins such as adenosine deaminase, caveolin-1, CXCR4, collagen, and fibronectin, while playing an important role in the regulation of inflammatory responses and tumor biology. We have focused on CD26 as a novel therapeutic target for various tumors and immune disorders, and have developed a humanized anti-CD26 monoclonal antibody (mAb), YS110, which is currently being evaluated in a phase I clinical trial for patients with CD26-expressing tumors, including malignant mesothelioma. Since detection of tumor CD26 expression is required for determining potential eligibility for YS110 therapy, the development of anti-human CD26 mAb that can clearly and reliably detect the denatured CD26 molecule in the formalin-fixed paraffin-embedded tissues is critical. METHODS: To develop novel anti-CD26 mAbs capable of binding to the denatured CD26, we immunized mice with CD26 protein denatured in urea buffer. After the fusion of splenocytes and myeloma cells, the mAbs were screened for specific reactivity with human CD26 by flow cytometry, enzyme-linked immunosorbent assay, and immunohistochemistry. The binding competitiveness of novel anti-CD26 mAbs with the humanized anti-CD26 mAb YS110 was also examined. RESULTS: We have succeeded in developing novel anti-human CD26 mAbs suitable for immunohistochemical staining of CD26 in formalin-fixed tissue sections with reliable clarity and intensity. Importantly, some of these mAbs exhibit no cross-reactivity with the humanized anti-CD26 mAb. CONCLUSIONS: These novel mAbs are potentially useful as companion diagnostic agents to analyze CD26 expression in the clinical setting while advancing future CD26-related research. VIRTUAL SLIDES: The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5987140221097729 BioMed Central 2014-02-06 /pmc/articles/PMC3944398/ /pubmed/24502396 http://dx.doi.org/10.1186/1746-1596-9-30 Text en Copyright © 2014 Hatano et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hatano, Ryo Yamada, Taketo Matsuoka, Shuji Iwata, Satoshi Yamazaki, Hiroto Komiya, Eriko Okamoto, Toshihiro Dang, Nam H Ohnuma, Kei Morimoto, Chikao Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue |
title | Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue |
title_full | Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue |
title_fullStr | Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue |
title_full_unstemmed | Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue |
title_short | Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue |
title_sort | establishment of monoclonal anti-human cd26 antibodies suitable for immunostaining of formalin-fixed tissue |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944398/ https://www.ncbi.nlm.nih.gov/pubmed/24502396 http://dx.doi.org/10.1186/1746-1596-9-30 |
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