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VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis
CX3CR1 has been identified as a highly attractive target for several therapeutic interventions. Despite this potential, no potent antagonists, either small molecule or monoclonal antibody, have been identified. Here we describe the lead finding and engineering approach that lead to the identificatio...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973309/ https://www.ncbi.nlm.nih.gov/pubmed/31924119 http://dx.doi.org/10.1080/19420862.2019.1709322 |
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author | Low, Sarah Wu, Haixia Jerath, Kavita Tibolla, Annette Fogal, Birgit Conrad, Rebecca MacDougall, Margit Kerr, Steven Berger, Valentina Dave, Rajvee Villalona, Jorge Pantages, Lynn Ahlberg, Jennifer Li, Hua Van Hoorick, Diane Ververken, Cedric Broadwater, John Waterman, Alisa Singh, Sanjaya Kroe-Barrett, Rachel |
author_facet | Low, Sarah Wu, Haixia Jerath, Kavita Tibolla, Annette Fogal, Birgit Conrad, Rebecca MacDougall, Margit Kerr, Steven Berger, Valentina Dave, Rajvee Villalona, Jorge Pantages, Lynn Ahlberg, Jennifer Li, Hua Van Hoorick, Diane Ververken, Cedric Broadwater, John Waterman, Alisa Singh, Sanjaya Kroe-Barrett, Rachel |
author_sort | Low, Sarah |
collection | PubMed |
description | CX3CR1 has been identified as a highly attractive target for several therapeutic interventions. Despite this potential, no potent antagonists, either small molecule or monoclonal antibody, have been identified. Here we describe the lead finding and engineering approach that lead to the identification of BI 655088, a potent biotherapeutic antagonist to CX3CR1. BI 655088 is a potent CX3CR1 antagonist that, upon therapeutic dosing, significantly inhibits plaque progression in the standard mouse model of atherosclerosis. BI 655088 represents a novel and highly selective biotherapeutic that could reduce inflammation in the atherosclerotic plaque when added to standard of care treatment including statins, which could result in a significant decrease in atherothrombotic events in patients with existing cardiovascular disease. |
format | Online Article Text |
id | pubmed-6973309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-69733092020-01-31 VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis Low, Sarah Wu, Haixia Jerath, Kavita Tibolla, Annette Fogal, Birgit Conrad, Rebecca MacDougall, Margit Kerr, Steven Berger, Valentina Dave, Rajvee Villalona, Jorge Pantages, Lynn Ahlberg, Jennifer Li, Hua Van Hoorick, Diane Ververken, Cedric Broadwater, John Waterman, Alisa Singh, Sanjaya Kroe-Barrett, Rachel MAbs Report CX3CR1 has been identified as a highly attractive target for several therapeutic interventions. Despite this potential, no potent antagonists, either small molecule or monoclonal antibody, have been identified. Here we describe the lead finding and engineering approach that lead to the identification of BI 655088, a potent biotherapeutic antagonist to CX3CR1. BI 655088 is a potent CX3CR1 antagonist that, upon therapeutic dosing, significantly inhibits plaque progression in the standard mouse model of atherosclerosis. BI 655088 represents a novel and highly selective biotherapeutic that could reduce inflammation in the atherosclerotic plaque when added to standard of care treatment including statins, which could result in a significant decrease in atherothrombotic events in patients with existing cardiovascular disease. Taylor & Francis 2020-01-10 /pmc/articles/PMC6973309/ /pubmed/31924119 http://dx.doi.org/10.1080/19420862.2019.1709322 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Report Low, Sarah Wu, Haixia Jerath, Kavita Tibolla, Annette Fogal, Birgit Conrad, Rebecca MacDougall, Margit Kerr, Steven Berger, Valentina Dave, Rajvee Villalona, Jorge Pantages, Lynn Ahlberg, Jennifer Li, Hua Van Hoorick, Diane Ververken, Cedric Broadwater, John Waterman, Alisa Singh, Sanjaya Kroe-Barrett, Rachel VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis |
title | VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis |
title_full | VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis |
title_fullStr | VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis |
title_full_unstemmed | VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis |
title_short | VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis |
title_sort | vhh antibody targeting the chemokine receptor cx3cr1 inhibits progression of atherosclerosis |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973309/ https://www.ncbi.nlm.nih.gov/pubmed/31924119 http://dx.doi.org/10.1080/19420862.2019.1709322 |
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