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Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice
Nano-antibodies possess great potential in many applications. However, they are naturally derived from heavy chain-only antibodies (HcAbs), which lack light chains and the CH1 domain, and are only found in camelids and sharks. In this study, we investigated whether the precise genetic removal of the...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167435/ https://www.ncbi.nlm.nih.gov/pubmed/30319646 http://dx.doi.org/10.3389/fimmu.2018.02202 |
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author | Zhang, Tianyi Cheng, Xueqian Yu, Di Lin, Fuyu Hou, Ning Cheng, Xuan Hao, Shanshan Wei, Jingjing Ma, Li Fu, Yanbin Ma, Yonghe Ren, Liming Han, Haitang Yu, Shuyang Yang, Xiao Zhao, Yaofeng |
author_facet | Zhang, Tianyi Cheng, Xueqian Yu, Di Lin, Fuyu Hou, Ning Cheng, Xuan Hao, Shanshan Wei, Jingjing Ma, Li Fu, Yanbin Ma, Yonghe Ren, Liming Han, Haitang Yu, Shuyang Yang, Xiao Zhao, Yaofeng |
author_sort | Zhang, Tianyi |
collection | PubMed |
description | Nano-antibodies possess great potential in many applications. However, they are naturally derived from heavy chain-only antibodies (HcAbs), which lack light chains and the CH1 domain, and are only found in camelids and sharks. In this study, we investigated whether the precise genetic removal of the CH1 exon of the γ1 gene enabled the production of a functional heavy chain-only IgG1 in mice. IgG1 heavy chain dimers lacking associated light chains were detected in the sera of the genetically modified mice. However, the genetic modification led to decreased expression of IgG1 but increased expression of other IgG subclasses. The genetically modified mice showed a weaker immune response to specific antigens compared with wild type mice. Using a phage-display approach, antigen-specific, single domain VH antibodies could be screened from the mice but exhibited much weaker antigen binding affinity than the conventional monoclonal antibodies. Although the strategy was only partially successful, this study confirms the feasibility of producing desirable nano-bodies with appropriate genetic modifications in mice. |
format | Online Article Text |
id | pubmed-6167435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61674352018-10-12 Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice Zhang, Tianyi Cheng, Xueqian Yu, Di Lin, Fuyu Hou, Ning Cheng, Xuan Hao, Shanshan Wei, Jingjing Ma, Li Fu, Yanbin Ma, Yonghe Ren, Liming Han, Haitang Yu, Shuyang Yang, Xiao Zhao, Yaofeng Front Immunol Immunology Nano-antibodies possess great potential in many applications. However, they are naturally derived from heavy chain-only antibodies (HcAbs), which lack light chains and the CH1 domain, and are only found in camelids and sharks. In this study, we investigated whether the precise genetic removal of the CH1 exon of the γ1 gene enabled the production of a functional heavy chain-only IgG1 in mice. IgG1 heavy chain dimers lacking associated light chains were detected in the sera of the genetically modified mice. However, the genetic modification led to decreased expression of IgG1 but increased expression of other IgG subclasses. The genetically modified mice showed a weaker immune response to specific antigens compared with wild type mice. Using a phage-display approach, antigen-specific, single domain VH antibodies could be screened from the mice but exhibited much weaker antigen binding affinity than the conventional monoclonal antibodies. Although the strategy was only partially successful, this study confirms the feasibility of producing desirable nano-bodies with appropriate genetic modifications in mice. Frontiers Media S.A. 2018-09-25 /pmc/articles/PMC6167435/ /pubmed/30319646 http://dx.doi.org/10.3389/fimmu.2018.02202 Text en Copyright © 2018 Zhang, Cheng, Yu, Lin, Hou, Cheng, Hao, Wei, Ma, Fu, Ma, Ren, Han, Yu, Yang and Zhao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Zhang, Tianyi Cheng, Xueqian Yu, Di Lin, Fuyu Hou, Ning Cheng, Xuan Hao, Shanshan Wei, Jingjing Ma, Li Fu, Yanbin Ma, Yonghe Ren, Liming Han, Haitang Yu, Shuyang Yang, Xiao Zhao, Yaofeng Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice |
title | Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice |
title_full | Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice |
title_fullStr | Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice |
title_full_unstemmed | Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice |
title_short | Genetic Removal of the CH1 Exon Enables the Production of Heavy Chain-Only IgG in Mice |
title_sort | genetic removal of the ch1 exon enables the production of heavy chain-only igg in mice |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167435/ https://www.ncbi.nlm.nih.gov/pubmed/30319646 http://dx.doi.org/10.3389/fimmu.2018.02202 |
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