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Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors
Peptide vaccination was developed for the prevention and therapy of acute and chronic infectious diseases and cancer. However, vaccine development is challenging, because the patient immune system requires the appropriate human leukocyte antigen (HLA) recognition with the peptide. Moreover, antigens...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940818/ https://www.ncbi.nlm.nih.gov/pubmed/31888191 http://dx.doi.org/10.3390/ijms20246337 |
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author | Kametani, Yoshie Ohno, Yusuke Ohshima, Shino Tsuda, Banri Yasuda, Atsushi Seki, Toshiro Ito, Ryoji Tokuda, Yutaka |
author_facet | Kametani, Yoshie Ohno, Yusuke Ohshima, Shino Tsuda, Banri Yasuda, Atsushi Seki, Toshiro Ito, Ryoji Tokuda, Yutaka |
author_sort | Kametani, Yoshie |
collection | PubMed |
description | Peptide vaccination was developed for the prevention and therapy of acute and chronic infectious diseases and cancer. However, vaccine development is challenging, because the patient immune system requires the appropriate human leukocyte antigen (HLA) recognition with the peptide. Moreover, antigens sometimes induce a low response, even if the peptide is presented by antigen-presenting cells and T cells recognize it. This is because the patient immunity is dampened or restricted by environmental factors. Even if the immune system responds appropriately, newly-developed immune checkpoint inhibitors (ICIs), which are used to increase the immune response against cancer, make the immune environment more complex. The ICIs may activate T cells, although the ratio of responsive patients is not high. However, the vaccine may induce some immune adverse effects in the presence of ICIs. Therefore, a system is needed to predict such risks. Humanized mouse systems possessing human immune cells have been developed to examine human immunity in vivo. One of the systems which uses transplanted human peripheral blood mononuclear cells (PBMCs) may become a new diagnosis strategy. Various humanized mouse systems are being developed and will become good tools for the prediction of antibody response and immune adverse effects. |
format | Online Article Text |
id | pubmed-6940818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69408182020-01-09 Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors Kametani, Yoshie Ohno, Yusuke Ohshima, Shino Tsuda, Banri Yasuda, Atsushi Seki, Toshiro Ito, Ryoji Tokuda, Yutaka Int J Mol Sci Review Peptide vaccination was developed for the prevention and therapy of acute and chronic infectious diseases and cancer. However, vaccine development is challenging, because the patient immune system requires the appropriate human leukocyte antigen (HLA) recognition with the peptide. Moreover, antigens sometimes induce a low response, even if the peptide is presented by antigen-presenting cells and T cells recognize it. This is because the patient immunity is dampened or restricted by environmental factors. Even if the immune system responds appropriately, newly-developed immune checkpoint inhibitors (ICIs), which are used to increase the immune response against cancer, make the immune environment more complex. The ICIs may activate T cells, although the ratio of responsive patients is not high. However, the vaccine may induce some immune adverse effects in the presence of ICIs. Therefore, a system is needed to predict such risks. Humanized mouse systems possessing human immune cells have been developed to examine human immunity in vivo. One of the systems which uses transplanted human peripheral blood mononuclear cells (PBMCs) may become a new diagnosis strategy. Various humanized mouse systems are being developed and will become good tools for the prediction of antibody response and immune adverse effects. MDPI 2019-12-16 /pmc/articles/PMC6940818/ /pubmed/31888191 http://dx.doi.org/10.3390/ijms20246337 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kametani, Yoshie Ohno, Yusuke Ohshima, Shino Tsuda, Banri Yasuda, Atsushi Seki, Toshiro Ito, Ryoji Tokuda, Yutaka Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors |
title | Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors |
title_full | Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors |
title_fullStr | Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors |
title_full_unstemmed | Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors |
title_short | Humanized Mice as an Effective Evaluation System for Peptide Vaccines and Immune Checkpoint Inhibitors |
title_sort | humanized mice as an effective evaluation system for peptide vaccines and immune checkpoint inhibitors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940818/ https://www.ncbi.nlm.nih.gov/pubmed/31888191 http://dx.doi.org/10.3390/ijms20246337 |
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