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The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice

Senotherapy targeting for senescent cells is designed to attenuate age-related dysfunction. Senescent T cells, defined as CD4(+) CD44(high) CD62L(low) PD-1(+) CD153(+) cells, accumulate in visceral adipose tissues (VAT) in obese individuals. Here, we show the long-lasting effect of using CD153 vacci...

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Autores principales: Yoshida, Shota, Nakagami, Hironori, Hayashi, Hiroki, Ikeda, Yuka, Sun, Jiao, Tenma, Akiko, Tomioka, Hideki, Kawano, Tomohiro, Shimamura, Munehisa, Morishita, Ryuichi, Rakugi, Hiromi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235045/
https://www.ncbi.nlm.nih.gov/pubmed/32424156
http://dx.doi.org/10.1038/s41467-020-16347-w
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author Yoshida, Shota
Nakagami, Hironori
Hayashi, Hiroki
Ikeda, Yuka
Sun, Jiao
Tenma, Akiko
Tomioka, Hideki
Kawano, Tomohiro
Shimamura, Munehisa
Morishita, Ryuichi
Rakugi, Hiromi
author_facet Yoshida, Shota
Nakagami, Hironori
Hayashi, Hiroki
Ikeda, Yuka
Sun, Jiao
Tenma, Akiko
Tomioka, Hideki
Kawano, Tomohiro
Shimamura, Munehisa
Morishita, Ryuichi
Rakugi, Hiromi
author_sort Yoshida, Shota
collection PubMed
description Senotherapy targeting for senescent cells is designed to attenuate age-related dysfunction. Senescent T cells, defined as CD4(+) CD44(high) CD62L(low) PD-1(+) CD153(+) cells, accumulate in visceral adipose tissues (VAT) in obese individuals. Here, we show the long-lasting effect of using CD153 vaccination to remove senescent T cells from high-fat diet (HFD)-induced obese C57BL/6J mice. We administered a CD153 peptide-KLH (keyhole limpet hemocyanin) conjugate vaccine with Alhydrogel (CD153-Alum) or CpG oligodeoxynucleotide (ODN) 1585 (CD153-CpG) and confirmed an increase in anti-CD153 antibody levels that was sustained for several months. After being fed a HFD for 10–11 weeks, adipose senescent T cell accumulation was significantly reduced in the VAT of CD153-CpG-vaccinated mice, accompanied by glucose tolerance and insulin resistance. A complement-dependent cytotoxicity (CDC) assay indicated that the mouse IgG2 antibody produced in the CD153-CpG-vaccinated mice successfully reduced the number of senescent T cells. The CD153-CpG vaccine is an optional tool for senolytic therapy.
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spelling pubmed-72350452020-05-20 The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice Yoshida, Shota Nakagami, Hironori Hayashi, Hiroki Ikeda, Yuka Sun, Jiao Tenma, Akiko Tomioka, Hideki Kawano, Tomohiro Shimamura, Munehisa Morishita, Ryuichi Rakugi, Hiromi Nat Commun Article Senotherapy targeting for senescent cells is designed to attenuate age-related dysfunction. Senescent T cells, defined as CD4(+) CD44(high) CD62L(low) PD-1(+) CD153(+) cells, accumulate in visceral adipose tissues (VAT) in obese individuals. Here, we show the long-lasting effect of using CD153 vaccination to remove senescent T cells from high-fat diet (HFD)-induced obese C57BL/6J mice. We administered a CD153 peptide-KLH (keyhole limpet hemocyanin) conjugate vaccine with Alhydrogel (CD153-Alum) or CpG oligodeoxynucleotide (ODN) 1585 (CD153-CpG) and confirmed an increase in anti-CD153 antibody levels that was sustained for several months. After being fed a HFD for 10–11 weeks, adipose senescent T cell accumulation was significantly reduced in the VAT of CD153-CpG-vaccinated mice, accompanied by glucose tolerance and insulin resistance. A complement-dependent cytotoxicity (CDC) assay indicated that the mouse IgG2 antibody produced in the CD153-CpG-vaccinated mice successfully reduced the number of senescent T cells. The CD153-CpG vaccine is an optional tool for senolytic therapy. Nature Publishing Group UK 2020-05-18 /pmc/articles/PMC7235045/ /pubmed/32424156 http://dx.doi.org/10.1038/s41467-020-16347-w Text en © The Author(s) 2020 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/.
spellingShingle Article
Yoshida, Shota
Nakagami, Hironori
Hayashi, Hiroki
Ikeda, Yuka
Sun, Jiao
Tenma, Akiko
Tomioka, Hideki
Kawano, Tomohiro
Shimamura, Munehisa
Morishita, Ryuichi
Rakugi, Hiromi
The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice
title The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice
title_full The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice
title_fullStr The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice
title_full_unstemmed The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice
title_short The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice
title_sort cd153 vaccine is a senotherapeutic option for preventing the accumulation of senescent t cells in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235045/
https://www.ncbi.nlm.nih.gov/pubmed/32424156
http://dx.doi.org/10.1038/s41467-020-16347-w
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