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Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing
The coronavirus disease 2019 pandemic has caused more than 532 million infections and 6.3 million deaths to date. The reactive and neutralizing fully human antibodies of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are effective detection tools and therapeutic measures. During SARS-C...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545174/ https://www.ncbi.nlm.nih.gov/pubmed/36211410 http://dx.doi.org/10.3389/fimmu.2022.992787 |
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author | Yang, Xi Chi, Hang Wu, Meng Wang, Zhenshan Lang, Qiaoli Han, Qiuxue Wang, Xinyue Liu, Xueqin Li, Yuanguo Wang, Xiwen Huang, Nan Bi, Jinhao Liang, Hao Gao, Yuwei Zhao, Yongkun Feng, Na Yang, Songtao Wang, Tiecheng Xia, Xianzhu Ge, Liangpeng |
author_facet | Yang, Xi Chi, Hang Wu, Meng Wang, Zhenshan Lang, Qiaoli Han, Qiuxue Wang, Xinyue Liu, Xueqin Li, Yuanguo Wang, Xiwen Huang, Nan Bi, Jinhao Liang, Hao Gao, Yuwei Zhao, Yongkun Feng, Na Yang, Songtao Wang, Tiecheng Xia, Xianzhu Ge, Liangpeng |
author_sort | Yang, Xi |
collection | PubMed |
description | The coronavirus disease 2019 pandemic has caused more than 532 million infections and 6.3 million deaths to date. The reactive and neutralizing fully human antibodies of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are effective detection tools and therapeutic measures. During SARS-CoV-2 infection, a large number of SARS-CoV-2 reactive and neutralizing antibodies will be produced. Most SARS-CoV-2 reactive and neutralizing fully human antibodies are isolated from human and frequently encoded by convergent heavy-chain variable genes. However, SARS-CoV-2 viruses can mutate rapidly during replication and the resistant variants of neutralizing antibodies easily survive and evade the immune response, especially in the face of such focused antibody responses in humans. Therefore, additional tools are needed to develop different kinds of fully human antibodies to compensate for current deficiency. In this study, we utilized antibody humanized CAMouse(HG) mice to develop a rapid antibody discovery method and examine the antibody repertoire of SARS-CoV-2 RBD-reactive hybridoma cells derived from CAMouse(HG) mice by using high-throughput single-cell V(D)J sequencing analysis. CAMouse(HG) mice were immunized by 28-day rapid immunization method. After electrofusion and semi-solid medium screening on day 12 post-electrofusion, 171 hybridoma clones were generated based on the results of SARS-CoV-2 RBD binding activity assay. A rather obvious preferential usage of IGHV6-1 family was found in these hybridoma clones derived from CAMouse(HG) mice, which was significantly different from the antibodies found in patients with COVID-19. After further virus neutralization screening and antibody competition assays, we generated a noncompeting two-antibody cocktail, which showed a potent prophylactic protective efficacy against SARS-CoV-2 in cynomolgus macaques. These results indicate that humanized CAMouse(HG) mice not only provide a valuable platform to obtain fully human reactive and neutralizing antibodies but also have a different antibody repertoire from humans. Thus, humanized CAMouse(HG) mice can be used as a good complementary tool in discovery of fully human therapeutic and diagnostic antibodies. |
format | Online Article Text |
id | pubmed-9545174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95451742022-10-08 Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing Yang, Xi Chi, Hang Wu, Meng Wang, Zhenshan Lang, Qiaoli Han, Qiuxue Wang, Xinyue Liu, Xueqin Li, Yuanguo Wang, Xiwen Huang, Nan Bi, Jinhao Liang, Hao Gao, Yuwei Zhao, Yongkun Feng, Na Yang, Songtao Wang, Tiecheng Xia, Xianzhu Ge, Liangpeng Front Immunol Immunology The coronavirus disease 2019 pandemic has caused more than 532 million infections and 6.3 million deaths to date. The reactive and neutralizing fully human antibodies of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are effective detection tools and therapeutic measures. During SARS-CoV-2 infection, a large number of SARS-CoV-2 reactive and neutralizing antibodies will be produced. Most SARS-CoV-2 reactive and neutralizing fully human antibodies are isolated from human and frequently encoded by convergent heavy-chain variable genes. However, SARS-CoV-2 viruses can mutate rapidly during replication and the resistant variants of neutralizing antibodies easily survive and evade the immune response, especially in the face of such focused antibody responses in humans. Therefore, additional tools are needed to develop different kinds of fully human antibodies to compensate for current deficiency. In this study, we utilized antibody humanized CAMouse(HG) mice to develop a rapid antibody discovery method and examine the antibody repertoire of SARS-CoV-2 RBD-reactive hybridoma cells derived from CAMouse(HG) mice by using high-throughput single-cell V(D)J sequencing analysis. CAMouse(HG) mice were immunized by 28-day rapid immunization method. After electrofusion and semi-solid medium screening on day 12 post-electrofusion, 171 hybridoma clones were generated based on the results of SARS-CoV-2 RBD binding activity assay. A rather obvious preferential usage of IGHV6-1 family was found in these hybridoma clones derived from CAMouse(HG) mice, which was significantly different from the antibodies found in patients with COVID-19. After further virus neutralization screening and antibody competition assays, we generated a noncompeting two-antibody cocktail, which showed a potent prophylactic protective efficacy against SARS-CoV-2 in cynomolgus macaques. These results indicate that humanized CAMouse(HG) mice not only provide a valuable platform to obtain fully human reactive and neutralizing antibodies but also have a different antibody repertoire from humans. Thus, humanized CAMouse(HG) mice can be used as a good complementary tool in discovery of fully human therapeutic and diagnostic antibodies. Frontiers Media S.A. 2022-09-23 /pmc/articles/PMC9545174/ /pubmed/36211410 http://dx.doi.org/10.3389/fimmu.2022.992787 Text en Copyright © 2022 Yang, Chi, Wu, Wang, Lang, Han, Wang, Liu, Li, Wang, Huang, Bi, Liang, Gao, Zhao, Feng, Yang, Wang, Xia and Ge https://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 Yang, Xi Chi, Hang Wu, Meng Wang, Zhenshan Lang, Qiaoli Han, Qiuxue Wang, Xinyue Liu, Xueqin Li, Yuanguo Wang, Xiwen Huang, Nan Bi, Jinhao Liang, Hao Gao, Yuwei Zhao, Yongkun Feng, Na Yang, Songtao Wang, Tiecheng Xia, Xianzhu Ge, Liangpeng Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing |
title | Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing |
title_full | Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing |
title_fullStr | Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing |
title_full_unstemmed | Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing |
title_short | Discovery and characterization of SARS-CoV-2 reactive and neutralizing antibodies from humanized CAMouse(HG) mice through rapid hybridoma screening and high-throughput single-cell V(D)J sequencing |
title_sort | discovery and characterization of sars-cov-2 reactive and neutralizing antibodies from humanized camouse(hg) mice through rapid hybridoma screening and high-throughput single-cell v(d)j sequencing |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545174/ https://www.ncbi.nlm.nih.gov/pubmed/36211410 http://dx.doi.org/10.3389/fimmu.2022.992787 |
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