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Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen

Type-1 diabetes (T1D) is a metabolic disease involving the autoimmune destruction of insulin-producing pancreatic beta cells. It is often diagnosed by the detection of autoantibodies, typically those recognizing insulin itself or the 65-kDa isoform of glutamic acid decarboxylase (GAD65). Oral insuli...

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Autores principales: Bertini, Edoardo, Merlin, Matilde, Gecchele, Elisa, Puggia, Andrea, Brozzetti, Annalisa, Commisso, Mauro, Falorni, Alberto, Bini, Vittorio, Klymyuk, Victor, Pezzotti, Mario, Avesani, Linda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5938395/
https://www.ncbi.nlm.nih.gov/pubmed/29765386
http://dx.doi.org/10.3389/fpls.2018.00572
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author Bertini, Edoardo
Merlin, Matilde
Gecchele, Elisa
Puggia, Andrea
Brozzetti, Annalisa
Commisso, Mauro
Falorni, Alberto
Bini, Vittorio
Klymyuk, Victor
Pezzotti, Mario
Avesani, Linda
author_facet Bertini, Edoardo
Merlin, Matilde
Gecchele, Elisa
Puggia, Andrea
Brozzetti, Annalisa
Commisso, Mauro
Falorni, Alberto
Bini, Vittorio
Klymyuk, Victor
Pezzotti, Mario
Avesani, Linda
author_sort Bertini, Edoardo
collection PubMed
description Type-1 diabetes (T1D) is a metabolic disease involving the autoimmune destruction of insulin-producing pancreatic beta cells. It is often diagnosed by the detection of autoantibodies, typically those recognizing insulin itself or the 65-kDa isoform of glutamic acid decarboxylase (GAD65). Oral insulin can be used to induce systemic immunological tolerance and thus prevent or delay the onset of T1D, suggesting that combination treatments with other autoantigens such as GAD65 could be even more successful. GAD65 has induced oral tolerance and prevented T1D in preclinical studies but it is difficult to produce in sufficient quantities for clinical testing. Here we combined edible plant systems, namely spinach (Spinacia oleracea cv Industra) and red beet (Beta vulgaris cv Moulin Rouge), with the magnICON(®) expression system to develop a safe, cost-effective and environmentally sustainable platform for the large-scale production of GAD65. The superior red beet platform was extensively characterized in terms of recombinant protein yields and bioequivalence to wild-type plants, and the product was tested for its ability to resist simulated gastric digestion. Our results indicate that red beet plants are suitable for the production of a candidate oral vaccine based on GAD65 for the future preclinical and clinical testing of T1D immunotherapy approaches.
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spelling pubmed-59383952018-05-14 Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen Bertini, Edoardo Merlin, Matilde Gecchele, Elisa Puggia, Andrea Brozzetti, Annalisa Commisso, Mauro Falorni, Alberto Bini, Vittorio Klymyuk, Victor Pezzotti, Mario Avesani, Linda Front Plant Sci Plant Science Type-1 diabetes (T1D) is a metabolic disease involving the autoimmune destruction of insulin-producing pancreatic beta cells. It is often diagnosed by the detection of autoantibodies, typically those recognizing insulin itself or the 65-kDa isoform of glutamic acid decarboxylase (GAD65). Oral insulin can be used to induce systemic immunological tolerance and thus prevent or delay the onset of T1D, suggesting that combination treatments with other autoantigens such as GAD65 could be even more successful. GAD65 has induced oral tolerance and prevented T1D in preclinical studies but it is difficult to produce in sufficient quantities for clinical testing. Here we combined edible plant systems, namely spinach (Spinacia oleracea cv Industra) and red beet (Beta vulgaris cv Moulin Rouge), with the magnICON(®) expression system to develop a safe, cost-effective and environmentally sustainable platform for the large-scale production of GAD65. The superior red beet platform was extensively characterized in terms of recombinant protein yields and bioequivalence to wild-type plants, and the product was tested for its ability to resist simulated gastric digestion. Our results indicate that red beet plants are suitable for the production of a candidate oral vaccine based on GAD65 for the future preclinical and clinical testing of T1D immunotherapy approaches. Frontiers Media S.A. 2018-05-01 /pmc/articles/PMC5938395/ /pubmed/29765386 http://dx.doi.org/10.3389/fpls.2018.00572 Text en Copyright © 2018 Bertini, Merlin, Gecchele, Puggia, Brozzetti, Commisso, Falorni, Bini, Klymyuk, Pezzotti and Avesani. 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 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 Plant Science
Bertini, Edoardo
Merlin, Matilde
Gecchele, Elisa
Puggia, Andrea
Brozzetti, Annalisa
Commisso, Mauro
Falorni, Alberto
Bini, Vittorio
Klymyuk, Victor
Pezzotti, Mario
Avesani, Linda
Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen
title Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen
title_full Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen
title_fullStr Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen
title_full_unstemmed Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen
title_short Design of a Type-1 Diabetes Vaccine Candidate Using Edible Plants Expressing a Major Autoantigen
title_sort design of a type-1 diabetes vaccine candidate using edible plants expressing a major autoantigen
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5938395/
https://www.ncbi.nlm.nih.gov/pubmed/29765386
http://dx.doi.org/10.3389/fpls.2018.00572
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