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Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines

The development of new and effective adjuvants may play a fundamental role in improving HIV vaccine efficacy. New classes of vaccine adjuvants activate innate immunity receptors, notably toll like receptors (TLRs). Adjuvants targeting the C-Type lectin receptor DC-SIGN may be alternative or compleme...

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Autores principales: Berzi, Angela, Varga, Norbert, Sattin, Sara, Antonazzo, Patrizio, Biasin, Mara, Cetin, Irene, Trabattoni, Daria, Bernardi, Anna, Clerici, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939462/
https://www.ncbi.nlm.nih.gov/pubmed/24473338
http://dx.doi.org/10.3390/v6020391
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author Berzi, Angela
Varga, Norbert
Sattin, Sara
Antonazzo, Patrizio
Biasin, Mara
Cetin, Irene
Trabattoni, Daria
Bernardi, Anna
Clerici, Mario
author_facet Berzi, Angela
Varga, Norbert
Sattin, Sara
Antonazzo, Patrizio
Biasin, Mara
Cetin, Irene
Trabattoni, Daria
Bernardi, Anna
Clerici, Mario
author_sort Berzi, Angela
collection PubMed
description The development of new and effective adjuvants may play a fundamental role in improving HIV vaccine efficacy. New classes of vaccine adjuvants activate innate immunity receptors, notably toll like receptors (TLRs). Adjuvants targeting the C-Type lectin receptor DC-SIGN may be alternative or complementary to adjuvants based on TRL activation. Herein we evaluate the ability of the glycomimetic DC-SIGN ligand Polyman 19 (PM 19) to modulate innate immune responses. Results showed that PM 19 alone, or in combination with TLR agonists, induces the expression of cytokines, β chemokines and co-stimulatory molecules that may, in turn, modulate adaptive immunity and exert anti-viral effects. These results indicate that the suitability of this compound as a vaccine adjuvant should be further evaluated.
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spelling pubmed-39394622014-03-03 Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines Berzi, Angela Varga, Norbert Sattin, Sara Antonazzo, Patrizio Biasin, Mara Cetin, Irene Trabattoni, Daria Bernardi, Anna Clerici, Mario Viruses Communication The development of new and effective adjuvants may play a fundamental role in improving HIV vaccine efficacy. New classes of vaccine adjuvants activate innate immunity receptors, notably toll like receptors (TLRs). Adjuvants targeting the C-Type lectin receptor DC-SIGN may be alternative or complementary to adjuvants based on TRL activation. Herein we evaluate the ability of the glycomimetic DC-SIGN ligand Polyman 19 (PM 19) to modulate innate immune responses. Results showed that PM 19 alone, or in combination with TLR agonists, induces the expression of cytokines, β chemokines and co-stimulatory molecules that may, in turn, modulate adaptive immunity and exert anti-viral effects. These results indicate that the suitability of this compound as a vaccine adjuvant should be further evaluated. MDPI 2014-01-27 /pmc/articles/PMC3939462/ /pubmed/24473338 http://dx.doi.org/10.3390/v6020391 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Berzi, Angela
Varga, Norbert
Sattin, Sara
Antonazzo, Patrizio
Biasin, Mara
Cetin, Irene
Trabattoni, Daria
Bernardi, Anna
Clerici, Mario
Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines
title Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines
title_full Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines
title_fullStr Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines
title_full_unstemmed Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines
title_short Pseudo-Mannosylated DC-SIGN Ligands as Potential Adjuvants for HIV Vaccines
title_sort pseudo-mannosylated dc-sign ligands as potential adjuvants for hiv vaccines
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939462/
https://www.ncbi.nlm.nih.gov/pubmed/24473338
http://dx.doi.org/10.3390/v6020391
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