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Programmable multispecific DNA-origami-based T-cell engagers
Multispecific antibodies have emerged as versatile therapeutic agents, and therefore, approaches to optimize and streamline their design and assembly are needed. Here we report on the modular and programmable assembly of IgG antibodies, F(ab) and scFv fragments on DNA origami nanocarriers. We screen...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656288/ https://www.ncbi.nlm.nih.gov/pubmed/37591933 http://dx.doi.org/10.1038/s41565-023-01471-7 |
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author | Wagenbauer, Klaus F. Pham, Nhi Gottschlich, Adrian Kick, Benjamin Kozina, Viktorija Frank, Christopher Trninic, Daniela Stömmer, Pierre Grünmeier, Ruth Carlini, Emanuele Tsiverioti, Christina Angeliki Kobold, Sebastian Funke, Jonas J. Dietz, Hendrik |
author_facet | Wagenbauer, Klaus F. Pham, Nhi Gottschlich, Adrian Kick, Benjamin Kozina, Viktorija Frank, Christopher Trninic, Daniela Stömmer, Pierre Grünmeier, Ruth Carlini, Emanuele Tsiverioti, Christina Angeliki Kobold, Sebastian Funke, Jonas J. Dietz, Hendrik |
author_sort | Wagenbauer, Klaus F. |
collection | PubMed |
description | Multispecific antibodies have emerged as versatile therapeutic agents, and therefore, approaches to optimize and streamline their design and assembly are needed. Here we report on the modular and programmable assembly of IgG antibodies, F(ab) and scFv fragments on DNA origami nanocarriers. We screened 105 distinct quadruplet antibody variants in vitro for the ability to activate T cells in the presence of target cells. T-cell engagers were identified, which in vitro showed the specific and efficient T-cell-mediated lysis of five distinct target cell lines. We used these T-cell engagers to target and lyse tumour cells in vivo in a xenograft mouse tumour model. Our approach enables the rapid generation, screening and testing of bi- and multispecific antibodies to facilitate preclinical pharmaceutical development from in vitro discovery to in vivo proof of concept. |
format | Online Article Text |
id | pubmed-10656288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106562882023-08-17 Programmable multispecific DNA-origami-based T-cell engagers Wagenbauer, Klaus F. Pham, Nhi Gottschlich, Adrian Kick, Benjamin Kozina, Viktorija Frank, Christopher Trninic, Daniela Stömmer, Pierre Grünmeier, Ruth Carlini, Emanuele Tsiverioti, Christina Angeliki Kobold, Sebastian Funke, Jonas J. Dietz, Hendrik Nat Nanotechnol Article Multispecific antibodies have emerged as versatile therapeutic agents, and therefore, approaches to optimize and streamline their design and assembly are needed. Here we report on the modular and programmable assembly of IgG antibodies, F(ab) and scFv fragments on DNA origami nanocarriers. We screened 105 distinct quadruplet antibody variants in vitro for the ability to activate T cells in the presence of target cells. T-cell engagers were identified, which in vitro showed the specific and efficient T-cell-mediated lysis of five distinct target cell lines. We used these T-cell engagers to target and lyse tumour cells in vivo in a xenograft mouse tumour model. Our approach enables the rapid generation, screening and testing of bi- and multispecific antibodies to facilitate preclinical pharmaceutical development from in vitro discovery to in vivo proof of concept. Nature Publishing Group UK 2023-08-17 2023 /pmc/articles/PMC10656288/ /pubmed/37591933 http://dx.doi.org/10.1038/s41565-023-01471-7 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wagenbauer, Klaus F. Pham, Nhi Gottschlich, Adrian Kick, Benjamin Kozina, Viktorija Frank, Christopher Trninic, Daniela Stömmer, Pierre Grünmeier, Ruth Carlini, Emanuele Tsiverioti, Christina Angeliki Kobold, Sebastian Funke, Jonas J. Dietz, Hendrik Programmable multispecific DNA-origami-based T-cell engagers |
title | Programmable multispecific DNA-origami-based T-cell engagers |
title_full | Programmable multispecific DNA-origami-based T-cell engagers |
title_fullStr | Programmable multispecific DNA-origami-based T-cell engagers |
title_full_unstemmed | Programmable multispecific DNA-origami-based T-cell engagers |
title_short | Programmable multispecific DNA-origami-based T-cell engagers |
title_sort | programmable multispecific dna-origami-based t-cell engagers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656288/ https://www.ncbi.nlm.nih.gov/pubmed/37591933 http://dx.doi.org/10.1038/s41565-023-01471-7 |
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