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Development of targeted adjuvants for HIV-1 vaccines

Finding new adjuvants is an integrated component of the efforts in developing an effective HIV-1 vaccine. Compared with traditional adjuvants, a modern adjuvant in the context of HIV-1 prevention would elicit a durable and potent memory response from B cells, CD8(+) T cells, and NK cells but avoid o...

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Detalles Bibliográficos
Autores principales: Liu, Jun, Ostrowski, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5594534/
https://www.ncbi.nlm.nih.gov/pubmed/28893282
http://dx.doi.org/10.1186/s12981-017-0165-8
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author Liu, Jun
Ostrowski, Mario
author_facet Liu, Jun
Ostrowski, Mario
author_sort Liu, Jun
collection PubMed
description Finding new adjuvants is an integrated component of the efforts in developing an effective HIV-1 vaccine. Compared with traditional adjuvants, a modern adjuvant in the context of HIV-1 prevention would elicit a durable and potent memory response from B cells, CD8(+) T cells, and NK cells but avoid overstimulation of HIV-1 susceptible CD4(+) T cells, especially at genital and rectal mucosa, the main portals for HIV-1 transmission. We briefly review recent advances in the studies of such potential targeted adjuvants, focusing on three classes of molecules that we study: TNFSF molecules, TLRs agonists, and NODs agonists.
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spelling pubmed-55945342017-09-14 Development of targeted adjuvants for HIV-1 vaccines Liu, Jun Ostrowski, Mario AIDS Res Ther Review Finding new adjuvants is an integrated component of the efforts in developing an effective HIV-1 vaccine. Compared with traditional adjuvants, a modern adjuvant in the context of HIV-1 prevention would elicit a durable and potent memory response from B cells, CD8(+) T cells, and NK cells but avoid overstimulation of HIV-1 susceptible CD4(+) T cells, especially at genital and rectal mucosa, the main portals for HIV-1 transmission. We briefly review recent advances in the studies of such potential targeted adjuvants, focusing on three classes of molecules that we study: TNFSF molecules, TLRs agonists, and NODs agonists. BioMed Central 2017-09-12 /pmc/articles/PMC5594534/ /pubmed/28893282 http://dx.doi.org/10.1186/s12981-017-0165-8 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Liu, Jun
Ostrowski, Mario
Development of targeted adjuvants for HIV-1 vaccines
title Development of targeted adjuvants for HIV-1 vaccines
title_full Development of targeted adjuvants for HIV-1 vaccines
title_fullStr Development of targeted adjuvants for HIV-1 vaccines
title_full_unstemmed Development of targeted adjuvants for HIV-1 vaccines
title_short Development of targeted adjuvants for HIV-1 vaccines
title_sort development of targeted adjuvants for hiv-1 vaccines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5594534/
https://www.ncbi.nlm.nih.gov/pubmed/28893282
http://dx.doi.org/10.1186/s12981-017-0165-8
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