Cargando…
CpG oligodeoxynucleotides as mucosal adjuvants
Bacterial DNA comprising palindromic sequences and containing unmethylated CpG is recognized by toll-like receptor 9 of plasmacytoid dendritic cells (pDCs) and induces the production of interferon-α and chemokines, leading to the activation of a Th1 immune response. Therefore, synthetic equivalents...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514178/ https://www.ncbi.nlm.nih.gov/pubmed/25751765 http://dx.doi.org/10.1080/21645515.2014.1004033 |
_version_ | 1782382745695027200 |
---|---|
author | Iho, Sumiko Maeyama, Jun-ichi Suzuki, Fumiko |
author_facet | Iho, Sumiko Maeyama, Jun-ichi Suzuki, Fumiko |
author_sort | Iho, Sumiko |
collection | PubMed |
description | Bacterial DNA comprising palindromic sequences and containing unmethylated CpG is recognized by toll-like receptor 9 of plasmacytoid dendritic cells (pDCs) and induces the production of interferon-α and chemokines, leading to the activation of a Th1 immune response. Therefore, synthetic equivalents of bacterial DNA (CpG oligodeoxynucleotides) have been developed for clinical applications. They are usually phosphorothioated for in vivo use; this approach also leads to adverse effects as reported in mouse models.Mucosal vaccines that induce both mucosal and systemic immunity received substantial attention in recent years. For their development, phosphodiester-linked oligodeoxynucleotides, including the sequence of a palindromic CpG DNA may be advantageous as adjuvants because their target pDCs are present right there, in the mucosa of the vaccination site. In addition, the probability of adverse effects is believed to be low. Here, we review the discovery of such CpG oligodeoxynucleotides and their possible use as mucosal adjuvants. |
format | Online Article Text |
id | pubmed-4514178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-45141782016-02-03 CpG oligodeoxynucleotides as mucosal adjuvants Iho, Sumiko Maeyama, Jun-ichi Suzuki, Fumiko Hum Vaccin Immunother Commentary Bacterial DNA comprising palindromic sequences and containing unmethylated CpG is recognized by toll-like receptor 9 of plasmacytoid dendritic cells (pDCs) and induces the production of interferon-α and chemokines, leading to the activation of a Th1 immune response. Therefore, synthetic equivalents of bacterial DNA (CpG oligodeoxynucleotides) have been developed for clinical applications. They are usually phosphorothioated for in vivo use; this approach also leads to adverse effects as reported in mouse models.Mucosal vaccines that induce both mucosal and systemic immunity received substantial attention in recent years. For their development, phosphodiester-linked oligodeoxynucleotides, including the sequence of a palindromic CpG DNA may be advantageous as adjuvants because their target pDCs are present right there, in the mucosa of the vaccination site. In addition, the probability of adverse effects is believed to be low. Here, we review the discovery of such CpG oligodeoxynucleotides and their possible use as mucosal adjuvants. Taylor & Francis 2015-03-09 /pmc/articles/PMC4514178/ /pubmed/25751765 http://dx.doi.org/10.1080/21645515.2014.1004033 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Commentary Iho, Sumiko Maeyama, Jun-ichi Suzuki, Fumiko CpG oligodeoxynucleotides as mucosal adjuvants |
title | CpG oligodeoxynucleotides as mucosal adjuvants |
title_full | CpG oligodeoxynucleotides as mucosal adjuvants |
title_fullStr | CpG oligodeoxynucleotides as mucosal adjuvants |
title_full_unstemmed | CpG oligodeoxynucleotides as mucosal adjuvants |
title_short | CpG oligodeoxynucleotides as mucosal adjuvants |
title_sort | cpg oligodeoxynucleotides as mucosal adjuvants |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514178/ https://www.ncbi.nlm.nih.gov/pubmed/25751765 http://dx.doi.org/10.1080/21645515.2014.1004033 |
work_keys_str_mv | AT ihosumiko cpgoligodeoxynucleotidesasmucosaladjuvants AT maeyamajunichi cpgoligodeoxynucleotidesasmucosaladjuvants AT suzukifumiko cpgoligodeoxynucleotidesasmucosaladjuvants |