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Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor

For clinical trials of therapeutic monoclonal antibodies (mAbs) to be successful, their efficacy needs to be adequately evaluated in preclinical experiments. However, in many cases it is difficult to evaluate the candidate mAbs using animal disease models because of lower cross-reactivity to the ort...

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Autores principales: Ueda, Otoya, Tateishi, Hiromi, Higuchi, Yoshinobu, Fujii, Etsuko, Kato, Atsuhiko, Kawase, Yosuke, Wada, Naoko A., Tachibe, Takanori, Kakefuda, Mami, Goto, Chisato, Kawaharada, Makoto, Shimaoka, Shin, Hattori, Kunihiro, Jishage, Kou-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561642/
https://www.ncbi.nlm.nih.gov/pubmed/23378927
http://dx.doi.org/10.1038/srep01196
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author Ueda, Otoya
Tateishi, Hiromi
Higuchi, Yoshinobu
Fujii, Etsuko
Kato, Atsuhiko
Kawase, Yosuke
Wada, Naoko A.
Tachibe, Takanori
Kakefuda, Mami
Goto, Chisato
Kawaharada, Makoto
Shimaoka, Shin
Hattori, Kunihiro
Jishage, Kou-ichi
author_facet Ueda, Otoya
Tateishi, Hiromi
Higuchi, Yoshinobu
Fujii, Etsuko
Kato, Atsuhiko
Kawase, Yosuke
Wada, Naoko A.
Tachibe, Takanori
Kakefuda, Mami
Goto, Chisato
Kawaharada, Makoto
Shimaoka, Shin
Hattori, Kunihiro
Jishage, Kou-ichi
author_sort Ueda, Otoya
collection PubMed
description For clinical trials of therapeutic monoclonal antibodies (mAbs) to be successful, their efficacy needs to be adequately evaluated in preclinical experiments. However, in many cases it is difficult to evaluate the candidate mAbs using animal disease models because of lower cross-reactivity to the orthologous target molecules. In this study we have established a novel humanized Castleman's disease mouse model, in which the endogenous interleukin-6 receptor gene is successfully replaced by human IL6R, and human IL6 is overexpressed. We have also demonstrated the therapeutic effects of an antibody that neutralizes human IL6R, tocilizumab, on the symptoms in this mouse model. Plasma levels of human soluble IL6R and human IL6 were elevated after 4-week treatment of tocilizumab in this mouse model similarly to the result previously reported in patients treated with tocilizumab. Our mouse model provides us with a novel means of evaluating the in vivo efficacy of human IL6R-specific therapeutic agents.
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spelling pubmed-35616422013-02-01 Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor Ueda, Otoya Tateishi, Hiromi Higuchi, Yoshinobu Fujii, Etsuko Kato, Atsuhiko Kawase, Yosuke Wada, Naoko A. Tachibe, Takanori Kakefuda, Mami Goto, Chisato Kawaharada, Makoto Shimaoka, Shin Hattori, Kunihiro Jishage, Kou-ichi Sci Rep Article For clinical trials of therapeutic monoclonal antibodies (mAbs) to be successful, their efficacy needs to be adequately evaluated in preclinical experiments. However, in many cases it is difficult to evaluate the candidate mAbs using animal disease models because of lower cross-reactivity to the orthologous target molecules. In this study we have established a novel humanized Castleman's disease mouse model, in which the endogenous interleukin-6 receptor gene is successfully replaced by human IL6R, and human IL6 is overexpressed. We have also demonstrated the therapeutic effects of an antibody that neutralizes human IL6R, tocilizumab, on the symptoms in this mouse model. Plasma levels of human soluble IL6R and human IL6 were elevated after 4-week treatment of tocilizumab in this mouse model similarly to the result previously reported in patients treated with tocilizumab. Our mouse model provides us with a novel means of evaluating the in vivo efficacy of human IL6R-specific therapeutic agents. Nature Publishing Group 2013-02-01 /pmc/articles/PMC3561642/ /pubmed/23378927 http://dx.doi.org/10.1038/srep01196 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Ueda, Otoya
Tateishi, Hiromi
Higuchi, Yoshinobu
Fujii, Etsuko
Kato, Atsuhiko
Kawase, Yosuke
Wada, Naoko A.
Tachibe, Takanori
Kakefuda, Mami
Goto, Chisato
Kawaharada, Makoto
Shimaoka, Shin
Hattori, Kunihiro
Jishage, Kou-ichi
Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor
title Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor
title_full Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor
title_fullStr Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor
title_full_unstemmed Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor
title_short Novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor
title_sort novel genetically-humanized mouse model established to evaluate efficacy of therapeutic agents to human interleukin-6 receptor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561642/
https://www.ncbi.nlm.nih.gov/pubmed/23378927
http://dx.doi.org/10.1038/srep01196
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