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Cell penetrating peptide: A potent delivery system in vaccine development
One of the main obstacles to most medication administrations (such as the vaccine constructs) is the cellular membrane’s inadequate permeability, which reduces their efficiency. Cell-penetrating peptides (CPPs) or protein transduction domains (PTDs) are well-known as potent biological nanocarriers t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679422/ https://www.ncbi.nlm.nih.gov/pubmed/36425579 http://dx.doi.org/10.3389/fphar.2022.1072685 |
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author | Hasannejad-Asl, Behnam Pooresmaeil, Farkhondeh Takamoli, Shahla Dabiri, Mehran Bolhassani, Azam |
author_facet | Hasannejad-Asl, Behnam Pooresmaeil, Farkhondeh Takamoli, Shahla Dabiri, Mehran Bolhassani, Azam |
author_sort | Hasannejad-Asl, Behnam |
collection | PubMed |
description | One of the main obstacles to most medication administrations (such as the vaccine constructs) is the cellular membrane’s inadequate permeability, which reduces their efficiency. Cell-penetrating peptides (CPPs) or protein transduction domains (PTDs) are well-known as potent biological nanocarriers to overcome this natural barrier, and to deliver membrane-impermeable substances into cells. The physicochemical properties of CPPs, the attached cargo, concentration, and cell type substantially influence the internalization mechanism. Although the exact mechanism of cellular uptake and the following processing of CPPs are still uncertain; but however, they can facilitate intracellular transfer through both endocytic and non-endocytic pathways. Improved endosomal escape efficiency, selective cell targeting, and improved uptake, processing, and presentation of antigen by antigen-presenting cells (APCs) have been reported by CPPs. Different in vitro and in vivo investigations using CPP conjugates show their potential as therapeutic agents in various medical areas such as infectious and non-infectious disorders. Effective treatments for a variety of diseases may be provided by vaccines that can cooperatively stimulate T cell-mediated immunity (T helper cell activity or cytotoxic T cell function), and immunologic memory. Delivery of antigen epitopes to APCs, and generation of a potent immune response is essential for an efficacious vaccine that can be facilitated by CPPs. The current review describes the delivery of numerous vaccine components by various CPPs and their immunostimulatory properties. |
format | Online Article Text |
id | pubmed-9679422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96794222022-11-23 Cell penetrating peptide: A potent delivery system in vaccine development Hasannejad-Asl, Behnam Pooresmaeil, Farkhondeh Takamoli, Shahla Dabiri, Mehran Bolhassani, Azam Front Pharmacol Pharmacology One of the main obstacles to most medication administrations (such as the vaccine constructs) is the cellular membrane’s inadequate permeability, which reduces their efficiency. Cell-penetrating peptides (CPPs) or protein transduction domains (PTDs) are well-known as potent biological nanocarriers to overcome this natural barrier, and to deliver membrane-impermeable substances into cells. The physicochemical properties of CPPs, the attached cargo, concentration, and cell type substantially influence the internalization mechanism. Although the exact mechanism of cellular uptake and the following processing of CPPs are still uncertain; but however, they can facilitate intracellular transfer through both endocytic and non-endocytic pathways. Improved endosomal escape efficiency, selective cell targeting, and improved uptake, processing, and presentation of antigen by antigen-presenting cells (APCs) have been reported by CPPs. Different in vitro and in vivo investigations using CPP conjugates show their potential as therapeutic agents in various medical areas such as infectious and non-infectious disorders. Effective treatments for a variety of diseases may be provided by vaccines that can cooperatively stimulate T cell-mediated immunity (T helper cell activity or cytotoxic T cell function), and immunologic memory. Delivery of antigen epitopes to APCs, and generation of a potent immune response is essential for an efficacious vaccine that can be facilitated by CPPs. The current review describes the delivery of numerous vaccine components by various CPPs and their immunostimulatory properties. Frontiers Media S.A. 2022-11-08 /pmc/articles/PMC9679422/ /pubmed/36425579 http://dx.doi.org/10.3389/fphar.2022.1072685 Text en Copyright © 2022 Hasannejad-Asl, Pooresmaeil, Takamoli, Dabiri and Bolhassani. https://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(s) 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 | Pharmacology Hasannejad-Asl, Behnam Pooresmaeil, Farkhondeh Takamoli, Shahla Dabiri, Mehran Bolhassani, Azam Cell penetrating peptide: A potent delivery system in vaccine development |
title | Cell penetrating peptide: A potent delivery system in vaccine development |
title_full | Cell penetrating peptide: A potent delivery system in vaccine development |
title_fullStr | Cell penetrating peptide: A potent delivery system in vaccine development |
title_full_unstemmed | Cell penetrating peptide: A potent delivery system in vaccine development |
title_short | Cell penetrating peptide: A potent delivery system in vaccine development |
title_sort | cell penetrating peptide: a potent delivery system in vaccine development |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679422/ https://www.ncbi.nlm.nih.gov/pubmed/36425579 http://dx.doi.org/10.3389/fphar.2022.1072685 |
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