Directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis

CXCR2 antagonism has been shown to be anti-arthritic, but anti-chemokine therapies usually fail in the clinic owing to redundancy in chemokine-receptor interactions. Here the authors develop single-chain antibodies with multiple chemokine specificities to achieve high affinity and broad specificity...

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Autores principales: Alessandro Angelini, Yoshishige Miyabe, Daniel Newsted, Byron H. Kwan, Chie Miyabe, Ryan L. Kelly, Misha N. Jamy, Andrew D. Luster, K. Dane Wittrup
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Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/c0b1123a348f40e095ceb7693a617ee1
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spelling oai:doaj.org-article:c0b1123a348f40e095ceb7693a617ee12021-12-02T15:34:38ZDirected evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis10.1038/s41467-018-03687-x2041-1723https://doaj.org/article/c0b1123a348f40e095ceb7693a617ee12018-04-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-03687-xhttps://doaj.org/toc/2041-1723CXCR2 antagonism has been shown to be anti-arthritic, but anti-chemokine therapies usually fail in the clinic owing to redundancy in chemokine-receptor interactions. Here the authors develop single-chain antibodies with multiple chemokine specificities to achieve high affinity and broad specificity to mouse and human CXC chemokines with efficacy in a K/BxN serum transfer model of arthritis.Alessandro AngeliniYoshishige MiyabeDaniel NewstedByron H. KwanChie MiyabeRyan L. KellyMisha N. JamyAndrew D. LusterK. Dane WittrupNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-18 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Alessandro Angelini
Yoshishige Miyabe
Daniel Newsted
Byron H. Kwan
Chie Miyabe
Ryan L. Kelly
Misha N. Jamy
Andrew D. Luster
K. Dane Wittrup
Directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis
description CXCR2 antagonism has been shown to be anti-arthritic, but anti-chemokine therapies usually fail in the clinic owing to redundancy in chemokine-receptor interactions. Here the authors develop single-chain antibodies with multiple chemokine specificities to achieve high affinity and broad specificity to mouse and human CXC chemokines with efficacy in a K/BxN serum transfer model of arthritis.
format article
author Alessandro Angelini
Yoshishige Miyabe
Daniel Newsted
Byron H. Kwan
Chie Miyabe
Ryan L. Kelly
Misha N. Jamy
Andrew D. Luster
K. Dane Wittrup
author_facet Alessandro Angelini
Yoshishige Miyabe
Daniel Newsted
Byron H. Kwan
Chie Miyabe
Ryan L. Kelly
Misha N. Jamy
Andrew D. Luster
K. Dane Wittrup
author_sort Alessandro Angelini
title Directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis
title_short Directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis
title_full Directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis
title_fullStr Directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis
title_full_unstemmed Directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis
title_sort directed evolution of broadly crossreactive chemokine-blocking antibodies efficacious in arthritis
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/c0b1123a348f40e095ceb7693a617ee1
work_keys_str_mv AT alessandroangelini directedevolutionofbroadlycrossreactivechemokineblockingantibodiesefficaciousinarthritis
AT yoshishigemiyabe directedevolutionofbroadlycrossreactivechemokineblockingantibodiesefficaciousinarthritis
AT danielnewsted directedevolutionofbroadlycrossreactivechemokineblockingantibodiesefficaciousinarthritis
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