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Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy
The RON receptor tyrosine kinase is an exceptionally interesting target in oncology and immunology. It is not only overexpressed in a wide variety of tumors but also has been shown to be expressed on myeloid cells associated with tumor infiltration, where it serves to dampen tumour immune responses...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800565/ https://www.ncbi.nlm.nih.gov/pubmed/36581692 http://dx.doi.org/10.1038/s41598-022-26404-7 |
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author | Yu Koh, Xin Koh, Xiao Hui Spiegelberg, Diana Jha, Preeti Nestor, Marika Hwang, Le-ann Tan, Ban Xiong Lane, David Philip |
author_facet | Yu Koh, Xin Koh, Xiao Hui Spiegelberg, Diana Jha, Preeti Nestor, Marika Hwang, Le-ann Tan, Ban Xiong Lane, David Philip |
author_sort | Yu Koh, Xin |
collection | PubMed |
description | The RON receptor tyrosine kinase is an exceptionally interesting target in oncology and immunology. It is not only overexpressed in a wide variety of tumors but also has been shown to be expressed on myeloid cells associated with tumor infiltration, where it serves to dampen tumour immune responses and reduce the efficacy of anti-CTLA4 therapy. Potent and selective inhibitory antibodies to RON might therefore both inhibit tumor cell growth and stimulate immune rejection of tumors. We derived cloned and sequenced a new panel of exceptionally avid anti-RON antibodies with picomolar binding affinities that inhibit MSP-induced RON signaling and show remarkable potency in antibody dependent cellular cytotoxicity. Antibody specificity was validated by cloning the antibody genes and creating recombinant antibodies and by the use of RON knock out cell lines. When radiolabeled with 89-Zirconium, the new antibodies 3F8 and 10G1 allow effective immuno-positron emission tomography (immunoPET) imaging of RON-expressing tumors and recognize universally exposed RON epitopes at the cell surface. The 10G1 was further developed into a novel bispecific T cell engager with a 15 pM EC50 in cytotoxic T cell killing assays. |
format | Online Article Text |
id | pubmed-9800565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98005652022-12-31 Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy Yu Koh, Xin Koh, Xiao Hui Spiegelberg, Diana Jha, Preeti Nestor, Marika Hwang, Le-ann Tan, Ban Xiong Lane, David Philip Sci Rep Article The RON receptor tyrosine kinase is an exceptionally interesting target in oncology and immunology. It is not only overexpressed in a wide variety of tumors but also has been shown to be expressed on myeloid cells associated with tumor infiltration, where it serves to dampen tumour immune responses and reduce the efficacy of anti-CTLA4 therapy. Potent and selective inhibitory antibodies to RON might therefore both inhibit tumor cell growth and stimulate immune rejection of tumors. We derived cloned and sequenced a new panel of exceptionally avid anti-RON antibodies with picomolar binding affinities that inhibit MSP-induced RON signaling and show remarkable potency in antibody dependent cellular cytotoxicity. Antibody specificity was validated by cloning the antibody genes and creating recombinant antibodies and by the use of RON knock out cell lines. When radiolabeled with 89-Zirconium, the new antibodies 3F8 and 10G1 allow effective immuno-positron emission tomography (immunoPET) imaging of RON-expressing tumors and recognize universally exposed RON epitopes at the cell surface. The 10G1 was further developed into a novel bispecific T cell engager with a 15 pM EC50 in cytotoxic T cell killing assays. Nature Publishing Group UK 2022-12-29 /pmc/articles/PMC9800565/ /pubmed/36581692 http://dx.doi.org/10.1038/s41598-022-26404-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yu Koh, Xin Koh, Xiao Hui Spiegelberg, Diana Jha, Preeti Nestor, Marika Hwang, Le-ann Tan, Ban Xiong Lane, David Philip Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy |
title | Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy |
title_full | Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy |
title_fullStr | Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy |
title_full_unstemmed | Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy |
title_short | Conformation specific antagonistic high affinity antibodies to the RON receptor kinase for imaging and therapy |
title_sort | conformation specific antagonistic high affinity antibodies to the ron receptor kinase for imaging and therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800565/ https://www.ncbi.nlm.nih.gov/pubmed/36581692 http://dx.doi.org/10.1038/s41598-022-26404-7 |
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