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Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector
Cytotoxic T lymphocyte-associated antigen 4 immunoglobulin fusion protein (CTLA4Ig, abatacept) is a B7/CD28 costimulation inhibitor that can ward off the immune response by preventing the activation of naïve T cells. This therapeutic agent is administered to patients with autoimmune diseases such as...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381501/ https://www.ncbi.nlm.nih.gov/pubmed/25374010 http://dx.doi.org/10.1038/srep06935 |
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author | Rim, Yeri Alice Yi, Hyoju Kim, Youngkyun Park, Narae Jung, Hyerin Kim, Juryun Jung, Seung Min Park, Sung-Hwan Ju, Ji Hyeon |
author_facet | Rim, Yeri Alice Yi, Hyoju Kim, Youngkyun Park, Narae Jung, Hyerin Kim, Juryun Jung, Seung Min Park, Sung-Hwan Ju, Ji Hyeon |
author_sort | Rim, Yeri Alice |
collection | PubMed |
description | Cytotoxic T lymphocyte-associated antigen 4 immunoglobulin fusion protein (CTLA4Ig, abatacept) is a B7/CD28 costimulation inhibitor that can ward off the immune response by preventing the activation of naïve T cells. This therapeutic agent is administered to patients with autoimmune diseases such as rheumatoid arthritis. Its antiarthritic efficacy is satisfactory, but the limitations are the necessity for frequent injection and high cost. Minicircles can robustly express the target molecule and excrete it outside the cell as an indirect method to produce the protein of interest in vivo. We inserted the sequence of abatacept into the minicircle vector, and by successful in vivo injection the host was able to produce the synthetic protein drug. Intravenous infusion of the minicircle induced spontaneous production of CTLA4Ig in mice with collagen-induced arthritis. Self-produced CTLA4Ig significantly decreased the symptoms of arthritis. Injection of minicircle CTLA4Ig regulated Foxp3(+) T cells and Th17 cells. Parental and mock vectors did not ameliorate arthritis or modify the T cell population. We have developed a new concept of spontaneous protein drug delivery using a minicircle vector. Self in vivo production of a synthetic protein drug may be useful when biological drugs cannot be injected because of manufacturing or practical problems. |
format | Online Article Text |
id | pubmed-5381501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53815012017-04-11 Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector Rim, Yeri Alice Yi, Hyoju Kim, Youngkyun Park, Narae Jung, Hyerin Kim, Juryun Jung, Seung Min Park, Sung-Hwan Ju, Ji Hyeon Sci Rep Article Cytotoxic T lymphocyte-associated antigen 4 immunoglobulin fusion protein (CTLA4Ig, abatacept) is a B7/CD28 costimulation inhibitor that can ward off the immune response by preventing the activation of naïve T cells. This therapeutic agent is administered to patients with autoimmune diseases such as rheumatoid arthritis. Its antiarthritic efficacy is satisfactory, but the limitations are the necessity for frequent injection and high cost. Minicircles can robustly express the target molecule and excrete it outside the cell as an indirect method to produce the protein of interest in vivo. We inserted the sequence of abatacept into the minicircle vector, and by successful in vivo injection the host was able to produce the synthetic protein drug. Intravenous infusion of the minicircle induced spontaneous production of CTLA4Ig in mice with collagen-induced arthritis. Self-produced CTLA4Ig significantly decreased the symptoms of arthritis. Injection of minicircle CTLA4Ig regulated Foxp3(+) T cells and Th17 cells. Parental and mock vectors did not ameliorate arthritis or modify the T cell population. We have developed a new concept of spontaneous protein drug delivery using a minicircle vector. Self in vivo production of a synthetic protein drug may be useful when biological drugs cannot be injected because of manufacturing or practical problems. Nature Publishing Group 2014-11-06 /pmc/articles/PMC5381501/ /pubmed/25374010 http://dx.doi.org/10.1038/srep06935 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Rim, Yeri Alice Yi, Hyoju Kim, Youngkyun Park, Narae Jung, Hyerin Kim, Juryun Jung, Seung Min Park, Sung-Hwan Ju, Ji Hyeon Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector |
title | Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector |
title_full | Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector |
title_fullStr | Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector |
title_full_unstemmed | Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector |
title_short | Self in vivo production of a synthetic biological drug CTLA4Ig using a minicircle vector |
title_sort | self in vivo production of a synthetic biological drug ctla4ig using a minicircle vector |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381501/ https://www.ncbi.nlm.nih.gov/pubmed/25374010 http://dx.doi.org/10.1038/srep06935 |
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