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An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance

Previously, we identified a therapy-resistant role of IL-34 in an immune checkpoint blockade in murine models. To investigate whether a similar mechanism is applicable in human tumors as well, we used this protocol for the selection of IL-34-neutralizing antibody and transplanting human tumor tissue...

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Autores principales: Han, Nanumi, Jang, Hye Yoon, Hama, Naoki, Kobayashi, Takuto, Otsuka, Ryo, Wada, Haruka, Seino, Ken-ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055705/
https://www.ncbi.nlm.nih.gov/pubmed/33899027
http://dx.doi.org/10.1016/j.xpro.2021.100460
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author Han, Nanumi
Jang, Hye Yoon
Hama, Naoki
Kobayashi, Takuto
Otsuka, Ryo
Wada, Haruka
Seino, Ken-ichiro
author_facet Han, Nanumi
Jang, Hye Yoon
Hama, Naoki
Kobayashi, Takuto
Otsuka, Ryo
Wada, Haruka
Seino, Ken-ichiro
author_sort Han, Nanumi
collection PubMed
description Previously, we identified a therapy-resistant role of IL-34 in an immune checkpoint blockade in murine models. To investigate whether a similar mechanism is applicable in human tumors as well, we used this protocol for the selection of IL-34-neutralizing antibody and transplanting human tumor tissue expressing both IL-34 and PD-L1 as a patient-derived xenograft in immunologically humanized mice. This model helps to determine the effect of IL-34 neutralization along with the immune checkpoint blockade in human tumors. For complete details on the use and execution of this protocol, please refer to Hama et al. (2020).
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spelling pubmed-80557052021-04-23 An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance Han, Nanumi Jang, Hye Yoon Hama, Naoki Kobayashi, Takuto Otsuka, Ryo Wada, Haruka Seino, Ken-ichiro STAR Protoc Protocol Previously, we identified a therapy-resistant role of IL-34 in an immune checkpoint blockade in murine models. To investigate whether a similar mechanism is applicable in human tumors as well, we used this protocol for the selection of IL-34-neutralizing antibody and transplanting human tumor tissue expressing both IL-34 and PD-L1 as a patient-derived xenograft in immunologically humanized mice. This model helps to determine the effect of IL-34 neutralization along with the immune checkpoint blockade in human tumors. For complete details on the use and execution of this protocol, please refer to Hama et al. (2020). Elsevier 2021-04-08 /pmc/articles/PMC8055705/ /pubmed/33899027 http://dx.doi.org/10.1016/j.xpro.2021.100460 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Han, Nanumi
Jang, Hye Yoon
Hama, Naoki
Kobayashi, Takuto
Otsuka, Ryo
Wada, Haruka
Seino, Ken-ichiro
An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance
title An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance
title_full An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance
title_fullStr An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance
title_full_unstemmed An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance
title_short An optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of IL-34 in immunotherapeutic resistance
title_sort optimized protocol for patient-derived xenograft in humanized mice to evaluate the role of il-34 in immunotherapeutic resistance
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055705/
https://www.ncbi.nlm.nih.gov/pubmed/33899027
http://dx.doi.org/10.1016/j.xpro.2021.100460
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