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Fc-fusion proteins: new developments and future perspectives
Since the first description in 1989 of CD4-Fc-fusion antagonists that inhibit human immune deficiency virus entry into T cells, Fc-fusion proteins have been intensely investigated for their effectiveness to curb a range of pathologies, with several notable recent successes coming to market. These pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491832/ https://www.ncbi.nlm.nih.gov/pubmed/22837174 http://dx.doi.org/10.1002/emmm.201201379 |
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author | Czajkowsky, Daniel M Hu, Jun Shao, Zhifeng Pleass, Richard J |
author_facet | Czajkowsky, Daniel M Hu, Jun Shao, Zhifeng Pleass, Richard J |
author_sort | Czajkowsky, Daniel M |
collection | PubMed |
description | Since the first description in 1989 of CD4-Fc-fusion antagonists that inhibit human immune deficiency virus entry into T cells, Fc-fusion proteins have been intensely investigated for their effectiveness to curb a range of pathologies, with several notable recent successes coming to market. These promising outcomes have stimulated the development of novel approaches to improve their efficacy and safety, while also broadening their clinical remit to other uses such as vaccines and intravenous immunoglobulin therapy. This increased attention has also led to non-clinical applications of Fc-fusions, such as affinity reagents in microarray devices. Here we discuss recent results and more generally applicable strategies to improve Fc-fusion proteins for each application, with particular attention to the newer, less charted areas. |
format | Online Article Text |
id | pubmed-3491832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-34918322012-11-09 Fc-fusion proteins: new developments and future perspectives Czajkowsky, Daniel M Hu, Jun Shao, Zhifeng Pleass, Richard J EMBO Mol Med Review Since the first description in 1989 of CD4-Fc-fusion antagonists that inhibit human immune deficiency virus entry into T cells, Fc-fusion proteins have been intensely investigated for their effectiveness to curb a range of pathologies, with several notable recent successes coming to market. These promising outcomes have stimulated the development of novel approaches to improve their efficacy and safety, while also broadening their clinical remit to other uses such as vaccines and intravenous immunoglobulin therapy. This increased attention has also led to non-clinical applications of Fc-fusions, such as affinity reagents in microarray devices. Here we discuss recent results and more generally applicable strategies to improve Fc-fusion proteins for each application, with particular attention to the newer, less charted areas. WILEY-VCH Verlag 2012-10 2012-07-26 /pmc/articles/PMC3491832/ /pubmed/22837174 http://dx.doi.org/10.1002/emmm.201201379 Text en Copyrights © 2012 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Review Czajkowsky, Daniel M Hu, Jun Shao, Zhifeng Pleass, Richard J Fc-fusion proteins: new developments and future perspectives |
title | Fc-fusion proteins: new developments and future perspectives |
title_full | Fc-fusion proteins: new developments and future perspectives |
title_fullStr | Fc-fusion proteins: new developments and future perspectives |
title_full_unstemmed | Fc-fusion proteins: new developments and future perspectives |
title_short | Fc-fusion proteins: new developments and future perspectives |
title_sort | fc-fusion proteins: new developments and future perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491832/ https://www.ncbi.nlm.nih.gov/pubmed/22837174 http://dx.doi.org/10.1002/emmm.201201379 |
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