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Novel neutralizing human monoclonal antibodies against tetanus neurotoxin
Tetanus is a fatal disease caused by tetanus neurotoxin (TeNT). TeNT is composed of a light chain (Lc) and a heavy chain, the latter of which is classified into two domains, N-terminus Hn and C-terminus Hc. Several TeNT-neutralizing antibodies have been reported, but it remains unclear which TeNT do...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190289/ https://www.ncbi.nlm.nih.gov/pubmed/34108521 http://dx.doi.org/10.1038/s41598-021-91597-2 |
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author | Minamitani, Takeharu Kiyose, Karin Otsubo, Ryota Ito, Toshihiro Akiba, Hiroki Furuta, Rika A. Inoue, Tsuyoshi Tsumoto, Kouhei Satake, Masahiro Yasui, Teruhito |
author_facet | Minamitani, Takeharu Kiyose, Karin Otsubo, Ryota Ito, Toshihiro Akiba, Hiroki Furuta, Rika A. Inoue, Tsuyoshi Tsumoto, Kouhei Satake, Masahiro Yasui, Teruhito |
author_sort | Minamitani, Takeharu |
collection | PubMed |
description | Tetanus is a fatal disease caused by tetanus neurotoxin (TeNT). TeNT is composed of a light chain (Lc) and a heavy chain, the latter of which is classified into two domains, N-terminus Hn and C-terminus Hc. Several TeNT-neutralizing antibodies have been reported, but it remains unclear which TeNT domains are involved in neutralization. To further understand the mechanism of these antibodies, we isolated TeNT-reactive human antibody clones from peripheral blood mononuclear cells. We then analyzed the reactivity of the isolated antibody clones to each protein domain and their inhibition of Hc-ganglioside GT1b binding, which is critical for TeNT toxicity. We also investigated the TeNT-neutralizing ability of isolated antibody clones and showed that an Hn-reactive clone protected strongly against TeNT toxicity in mice. Furthermore, combination treatment of Hn-reactive antibody clones with both Hc-reactive and TeNT mix (the mixture of Hc, Hn, and Lc proteins)–reactive antibody clones enhanced the neutralizing effect. These results indicated that antibody clones targeting Hn effectively neutralized TeNT. In addition, the use of a cocktail composed of Hc-, Hn-, and TeNT mix–reactive antibodies provided enhanced protection compared to the use of each antibody alone. |
format | Online Article Text |
id | pubmed-8190289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81902892021-06-10 Novel neutralizing human monoclonal antibodies against tetanus neurotoxin Minamitani, Takeharu Kiyose, Karin Otsubo, Ryota Ito, Toshihiro Akiba, Hiroki Furuta, Rika A. Inoue, Tsuyoshi Tsumoto, Kouhei Satake, Masahiro Yasui, Teruhito Sci Rep Article Tetanus is a fatal disease caused by tetanus neurotoxin (TeNT). TeNT is composed of a light chain (Lc) and a heavy chain, the latter of which is classified into two domains, N-terminus Hn and C-terminus Hc. Several TeNT-neutralizing antibodies have been reported, but it remains unclear which TeNT domains are involved in neutralization. To further understand the mechanism of these antibodies, we isolated TeNT-reactive human antibody clones from peripheral blood mononuclear cells. We then analyzed the reactivity of the isolated antibody clones to each protein domain and their inhibition of Hc-ganglioside GT1b binding, which is critical for TeNT toxicity. We also investigated the TeNT-neutralizing ability of isolated antibody clones and showed that an Hn-reactive clone protected strongly against TeNT toxicity in mice. Furthermore, combination treatment of Hn-reactive antibody clones with both Hc-reactive and TeNT mix (the mixture of Hc, Hn, and Lc proteins)–reactive antibody clones enhanced the neutralizing effect. These results indicated that antibody clones targeting Hn effectively neutralized TeNT. In addition, the use of a cocktail composed of Hc-, Hn-, and TeNT mix–reactive antibodies provided enhanced protection compared to the use of each antibody alone. Nature Publishing Group UK 2021-06-09 /pmc/articles/PMC8190289/ /pubmed/34108521 http://dx.doi.org/10.1038/s41598-021-91597-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Minamitani, Takeharu Kiyose, Karin Otsubo, Ryota Ito, Toshihiro Akiba, Hiroki Furuta, Rika A. Inoue, Tsuyoshi Tsumoto, Kouhei Satake, Masahiro Yasui, Teruhito Novel neutralizing human monoclonal antibodies against tetanus neurotoxin |
title | Novel neutralizing human monoclonal antibodies against tetanus neurotoxin |
title_full | Novel neutralizing human monoclonal antibodies against tetanus neurotoxin |
title_fullStr | Novel neutralizing human monoclonal antibodies against tetanus neurotoxin |
title_full_unstemmed | Novel neutralizing human monoclonal antibodies against tetanus neurotoxin |
title_short | Novel neutralizing human monoclonal antibodies against tetanus neurotoxin |
title_sort | novel neutralizing human monoclonal antibodies against tetanus neurotoxin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190289/ https://www.ncbi.nlm.nih.gov/pubmed/34108521 http://dx.doi.org/10.1038/s41598-021-91597-2 |
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