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Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies
For the recovery or replacement of dysfunctional cells and tissue—the goal of stem cell research—successful engraftment of transplanted cells and tissues are essential events. The event is largely dependent on the immune rejection of the recipient; therefore, the immunogenic evaluation of candidate...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909568/ https://www.ncbi.nlm.nih.gov/pubmed/33498509 http://dx.doi.org/10.3390/pharmaceutics13020130 |
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author | Kim, Yoon-Young Kim, Jin-Soo Che, Jeong-Hwan Ku, Seung-Yup Kang, Byeong-Cheol Yun, Jun-Won |
author_facet | Kim, Yoon-Young Kim, Jin-Soo Che, Jeong-Hwan Ku, Seung-Yup Kang, Byeong-Cheol Yun, Jun-Won |
author_sort | Kim, Yoon-Young |
collection | PubMed |
description | For the recovery or replacement of dysfunctional cells and tissue—the goal of stem cell research—successful engraftment of transplanted cells and tissues are essential events. The event is largely dependent on the immune rejection of the recipient; therefore, the immunogenic evaluation of candidate cells or tissues in immunodeficient animals is important. Understanding the immunodeficient system can provide insights into the generation and use of immunodeficient animal models, presenting a unique system to explore the capabilities of the innate immune system. In this review, we summarize various immunodeficient animal model systems with different target genes as valuable tools for biomedical research. There have been numerous immunodeficient models developed by different gene defects, resulting in many different features in phenotype. More important, mice, rats, and other large animals exhibit very different immunological and physiological features in tissue and organs, including genetic background and a representation of human disease conditions. Therefore, the findings from this review may guide researchers to select the most appropriate immunodeficient strain, target gene, and animal species based on the research type, mutant gene effects, and similarity to human immunological features for stem cell research. |
format | Online Article Text |
id | pubmed-7909568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79095682021-02-27 Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies Kim, Yoon-Young Kim, Jin-Soo Che, Jeong-Hwan Ku, Seung-Yup Kang, Byeong-Cheol Yun, Jun-Won Pharmaceutics Review For the recovery or replacement of dysfunctional cells and tissue—the goal of stem cell research—successful engraftment of transplanted cells and tissues are essential events. The event is largely dependent on the immune rejection of the recipient; therefore, the immunogenic evaluation of candidate cells or tissues in immunodeficient animals is important. Understanding the immunodeficient system can provide insights into the generation and use of immunodeficient animal models, presenting a unique system to explore the capabilities of the innate immune system. In this review, we summarize various immunodeficient animal model systems with different target genes as valuable tools for biomedical research. There have been numerous immunodeficient models developed by different gene defects, resulting in many different features in phenotype. More important, mice, rats, and other large animals exhibit very different immunological and physiological features in tissue and organs, including genetic background and a representation of human disease conditions. Therefore, the findings from this review may guide researchers to select the most appropriate immunodeficient strain, target gene, and animal species based on the research type, mutant gene effects, and similarity to human immunological features for stem cell research. MDPI 2021-01-20 /pmc/articles/PMC7909568/ /pubmed/33498509 http://dx.doi.org/10.3390/pharmaceutics13020130 Text en © 2021 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 Kim, Yoon-Young Kim, Jin-Soo Che, Jeong-Hwan Ku, Seung-Yup Kang, Byeong-Cheol Yun, Jun-Won Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies |
title | Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies |
title_full | Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies |
title_fullStr | Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies |
title_full_unstemmed | Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies |
title_short | Comparison of Genetically Engineered Immunodeficient Animal Models for Nonclinical Testing of Stem Cell Therapies |
title_sort | comparison of genetically engineered immunodeficient animal models for nonclinical testing of stem cell therapies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909568/ https://www.ncbi.nlm.nih.gov/pubmed/33498509 http://dx.doi.org/10.3390/pharmaceutics13020130 |
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