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Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA

Shiga toxin is a major virulence factor of food-poisoning caused by Escherichia coli such as O157:H7. Secretory immunoglobulin (Ig) A (SIgA) is supposed to prevent infection of the mucosal surface and is a candidate agent for oral immunotherapy. We previously established a recombinant monoclonal ant...

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Autores principales: Nakanishi, Katsuhiro, Morikane, Shota, Ichikawa, Shiori, Kurohane, Kohta, Niwa, Yasuo, Akimoto, Yoshihiro, Matsubara, Sachie, Kawakami, Hayato, Kobayashi, Hirokazu, Imai, Yasuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377459/
https://www.ncbi.nlm.nih.gov/pubmed/28368034
http://dx.doi.org/10.1038/srep45843
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author Nakanishi, Katsuhiro
Morikane, Shota
Ichikawa, Shiori
Kurohane, Kohta
Niwa, Yasuo
Akimoto, Yoshihiro
Matsubara, Sachie
Kawakami, Hayato
Kobayashi, Hirokazu
Imai, Yasuyuki
author_facet Nakanishi, Katsuhiro
Morikane, Shota
Ichikawa, Shiori
Kurohane, Kohta
Niwa, Yasuo
Akimoto, Yoshihiro
Matsubara, Sachie
Kawakami, Hayato
Kobayashi, Hirokazu
Imai, Yasuyuki
author_sort Nakanishi, Katsuhiro
collection PubMed
description Shiga toxin is a major virulence factor of food-poisoning caused by Escherichia coli such as O157:H7. Secretory immunoglobulin (Ig) A (SIgA) is supposed to prevent infection of the mucosal surface and is a candidate agent for oral immunotherapy. We previously established a recombinant monoclonal antibody (mAb) consisting of variable regions from a mouse IgG mAb specific for the binding subunit of Shiga toxin 1 (Stx1) and the Fc region of mouse IgA. Here we produced a secretory form of the recombinant IgA (S-hyIgA) with transgenic Arabidopsis thaliana plant. All the S-hyIgA cDNAs (heavy, light, J chain and secretory component) were expressed under the control of a bidirectional promoter of a chlorophyll a/b-binding protein of A. thaliana without using a viral promoter. The plant-based S-hyIgA exhibited antigen binding, and was modified with plant-specific N-linked sugar chains. The Ig heavy chain and secretory components were observed in an intracellular protein body-like structure of the transgenic leaves on immuno-electron microscopy. An extract of the transgenic leaves neutralized the cytotoxicity of Stx1 toward butyrate-treated Caco-2 cells, a human colon carcinoma cell line. These results will contribute to the development of edible therapeutic antibodies such as those for the treatment of mucosal infection.
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spelling pubmed-53774592017-04-10 Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA Nakanishi, Katsuhiro Morikane, Shota Ichikawa, Shiori Kurohane, Kohta Niwa, Yasuo Akimoto, Yoshihiro Matsubara, Sachie Kawakami, Hayato Kobayashi, Hirokazu Imai, Yasuyuki Sci Rep Article Shiga toxin is a major virulence factor of food-poisoning caused by Escherichia coli such as O157:H7. Secretory immunoglobulin (Ig) A (SIgA) is supposed to prevent infection of the mucosal surface and is a candidate agent for oral immunotherapy. We previously established a recombinant monoclonal antibody (mAb) consisting of variable regions from a mouse IgG mAb specific for the binding subunit of Shiga toxin 1 (Stx1) and the Fc region of mouse IgA. Here we produced a secretory form of the recombinant IgA (S-hyIgA) with transgenic Arabidopsis thaliana plant. All the S-hyIgA cDNAs (heavy, light, J chain and secretory component) were expressed under the control of a bidirectional promoter of a chlorophyll a/b-binding protein of A. thaliana without using a viral promoter. The plant-based S-hyIgA exhibited antigen binding, and was modified with plant-specific N-linked sugar chains. The Ig heavy chain and secretory components were observed in an intracellular protein body-like structure of the transgenic leaves on immuno-electron microscopy. An extract of the transgenic leaves neutralized the cytotoxicity of Stx1 toward butyrate-treated Caco-2 cells, a human colon carcinoma cell line. These results will contribute to the development of edible therapeutic antibodies such as those for the treatment of mucosal infection. Nature Publishing Group 2017-04-03 /pmc/articles/PMC5377459/ /pubmed/28368034 http://dx.doi.org/10.1038/srep45843 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Nakanishi, Katsuhiro
Morikane, Shota
Ichikawa, Shiori
Kurohane, Kohta
Niwa, Yasuo
Akimoto, Yoshihiro
Matsubara, Sachie
Kawakami, Hayato
Kobayashi, Hirokazu
Imai, Yasuyuki
Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA
title Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA
title_full Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA
title_fullStr Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA
title_full_unstemmed Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA
title_short Protection of Human Colon Cells from Shiga Toxin by Plant-based Recombinant Secretory IgA
title_sort protection of human colon cells from shiga toxin by plant-based recombinant secretory iga
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377459/
https://www.ncbi.nlm.nih.gov/pubmed/28368034
http://dx.doi.org/10.1038/srep45843
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