A deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications
Mett et al. describe development of GP532, a substantially deimmunized derivative of Toll-like receptor 5 (TLR5) agonist entolimod. GP532 has mutations eliminating key B- and T-cell epitopes and an inflammasome-activating domain yet remains a potent NF-κB activator with biological effects similar to...
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Nature Portfolio
2021
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oai:doaj.org-article:bcafc6dab7b74c02bc2aec45e9ac993a2021-12-02T14:26:12ZA deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications10.1038/s42003-021-01978-62399-3642https://doaj.org/article/bcafc6dab7b74c02bc2aec45e9ac993a2021-04-01T00:00:00Zhttps://doi.org/10.1038/s42003-021-01978-6https://doaj.org/toc/2399-3642Mett et al. describe development of GP532, a substantially deimmunized derivative of Toll-like receptor 5 (TLR5) agonist entolimod. GP532 has mutations eliminating key B- and T-cell epitopes and an inflammasome-activating domain yet remains a potent NF-κB activator with biological effects similar to entolimod. Thus, GP532 is suitable for multi-dose TLR5-targeting therapies and patients with high titers of preexisting flagellin-neutralizing antibodies.Vadim MettOleg V. KurnasovIvan A. BespalovIvan MolodtsovCraig M. BrackettLyudmila G. BurdelyaAndrei A. PurmalAnatoli S. GleibermanIlia A. ToshkovCatherine A. BurkhartYakov N. KoganEkaterina L. AndrianovaAndrei V. GudkovAndrei L. OstermanNature PortfolioarticleBiology (General)QH301-705.5ENCommunications Biology, Vol 4, Iss 1, Pp 1-14 (2021) |
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Biology (General) QH301-705.5 |
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Biology (General) QH301-705.5 Vadim Mett Oleg V. Kurnasov Ivan A. Bespalov Ivan Molodtsov Craig M. Brackett Lyudmila G. Burdelya Andrei A. Purmal Anatoli S. Gleiberman Ilia A. Toshkov Catherine A. Burkhart Yakov N. Kogan Ekaterina L. Andrianova Andrei V. Gudkov Andrei L. Osterman A deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications |
description |
Mett et al. describe development of GP532, a substantially deimmunized derivative of Toll-like receptor 5 (TLR5) agonist entolimod. GP532 has mutations eliminating key B- and T-cell epitopes and an inflammasome-activating domain yet remains a potent NF-κB activator with biological effects similar to entolimod. Thus, GP532 is suitable for multi-dose TLR5-targeting therapies and patients with high titers of preexisting flagellin-neutralizing antibodies. |
format |
article |
author |
Vadim Mett Oleg V. Kurnasov Ivan A. Bespalov Ivan Molodtsov Craig M. Brackett Lyudmila G. Burdelya Andrei A. Purmal Anatoli S. Gleiberman Ilia A. Toshkov Catherine A. Burkhart Yakov N. Kogan Ekaterina L. Andrianova Andrei V. Gudkov Andrei L. Osterman |
author_facet |
Vadim Mett Oleg V. Kurnasov Ivan A. Bespalov Ivan Molodtsov Craig M. Brackett Lyudmila G. Burdelya Andrei A. Purmal Anatoli S. Gleiberman Ilia A. Toshkov Catherine A. Burkhart Yakov N. Kogan Ekaterina L. Andrianova Andrei V. Gudkov Andrei L. Osterman |
author_sort |
Vadim Mett |
title |
A deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications |
title_short |
A deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications |
title_full |
A deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications |
title_fullStr |
A deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications |
title_full_unstemmed |
A deimmunized and pharmacologically optimized Toll-like receptor 5 agonist for therapeutic applications |
title_sort |
deimmunized and pharmacologically optimized toll-like receptor 5 agonist for therapeutic applications |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/bcafc6dab7b74c02bc2aec45e9ac993a |
work_keys_str_mv |
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