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Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus

Appropriate adjuvant selection may be essential to optimize the potency and to tailor the immune response of subunit vaccines. To induce protective responses against respiratory syncytial virus (RSV)—a highly prevalent childhood pathogen without a licensed vaccine—we previously engineered a pre-fusi...

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Autores principales: Sastry, Mallika, Zhang, Baoshan, Chen, Man, Joyce, M. Gordon, Kong, Wing-Pui, Chuang, Gwo-Yu, Ko, Kiyoon, Kumar, Azad, Silacci, Chiara, Thom, Michelle, Salazar, Andres M., Corti, Davide, Lanzavecchia, Antonio, Taylor, Geraldine, Mascola, John R., Graham, Barney S., Kwong, Peter D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658087/
https://www.ncbi.nlm.nih.gov/pubmed/29073183
http://dx.doi.org/10.1371/journal.pone.0186854
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author Sastry, Mallika
Zhang, Baoshan
Chen, Man
Joyce, M. Gordon
Kong, Wing-Pui
Chuang, Gwo-Yu
Ko, Kiyoon
Kumar, Azad
Silacci, Chiara
Thom, Michelle
Salazar, Andres M.
Corti, Davide
Lanzavecchia, Antonio
Taylor, Geraldine
Mascola, John R.
Graham, Barney S.
Kwong, Peter D.
author_facet Sastry, Mallika
Zhang, Baoshan
Chen, Man
Joyce, M. Gordon
Kong, Wing-Pui
Chuang, Gwo-Yu
Ko, Kiyoon
Kumar, Azad
Silacci, Chiara
Thom, Michelle
Salazar, Andres M.
Corti, Davide
Lanzavecchia, Antonio
Taylor, Geraldine
Mascola, John R.
Graham, Barney S.
Kwong, Peter D.
author_sort Sastry, Mallika
collection PubMed
description Appropriate adjuvant selection may be essential to optimize the potency and to tailor the immune response of subunit vaccines. To induce protective responses against respiratory syncytial virus (RSV)—a highly prevalent childhood pathogen without a licensed vaccine—we previously engineered a pre-fusion-stabilized trimeric RSV F (pre-F) “DS-Cav1” immunogen, which induced high titer RSV-neutralizing antibodies, in mice and non-human primates, when formulated with adjuvants Poly (I:C) and Poly (IC:LC), respectively. To assess the impact of different adjuvants, here we formulated RSV F DS-Cav1 with multiple adjuvants and assessed immune responses. Very high RSV-neutralizing antibody responses (19,006 EC(50)) were observed in naïve mice immunized with 2 doses of DS-Cav1 adjuvanted with Sigma adjuvant system (SAS), an oil-in-water adjuvant, plus Carbopol; high responses (3658–7108) were observed with DS-Cav1 adjuvanted with Alum, SAS alone, Adjuplex, Poly (I:C) and Poly (IC:LC); and moderate responses (1251–2129) were observed with DS-Cav1 adjuvanted with the TLR4 agonist MPLA, Alum plus MPLA or AddaVax. In contrast, DS-Cav1 without adjuvant induced low-level responses (6). A balanced IgG1 and IgG2a (Th2/Th1) immune response was elicited in most of the high to very high response groups (all but Alum and Adjuplex). We also tested the immune response induced by DS-Cav1 in elderly mice with pre-existing DS-Cav1 immunity; we observed that DS-Cav1 adjuvanted with SAS plus Carbopol boosted the response 2-3-fold, whereas DS-Cav1 adjuvanted with alum boosted the response 5-fold. Finally, we tested whether a mixture of ISA 71 VG and Carbopol would enhanced the antibody response in DS-Cav1 immunized calves. While pre-F-stabilized bovine RSV F induced very high titers in mice when adjuvanted with SAS plus Carbopol, the addition of Carbopol to ISA 71 VG did not enhance immune responses in calves. The vaccine response to pre-F-stabilized RSV F is augmented by adjuvant, but the degree of adjuvant-induced enhancement appears to be both context-dependent and species-specific.
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spelling pubmed-56580872017-11-09 Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus Sastry, Mallika Zhang, Baoshan Chen, Man Joyce, M. Gordon Kong, Wing-Pui Chuang, Gwo-Yu Ko, Kiyoon Kumar, Azad Silacci, Chiara Thom, Michelle Salazar, Andres M. Corti, Davide Lanzavecchia, Antonio Taylor, Geraldine Mascola, John R. Graham, Barney S. Kwong, Peter D. PLoS One Research Article Appropriate adjuvant selection may be essential to optimize the potency and to tailor the immune response of subunit vaccines. To induce protective responses against respiratory syncytial virus (RSV)—a highly prevalent childhood pathogen without a licensed vaccine—we previously engineered a pre-fusion-stabilized trimeric RSV F (pre-F) “DS-Cav1” immunogen, which induced high titer RSV-neutralizing antibodies, in mice and non-human primates, when formulated with adjuvants Poly (I:C) and Poly (IC:LC), respectively. To assess the impact of different adjuvants, here we formulated RSV F DS-Cav1 with multiple adjuvants and assessed immune responses. Very high RSV-neutralizing antibody responses (19,006 EC(50)) were observed in naïve mice immunized with 2 doses of DS-Cav1 adjuvanted with Sigma adjuvant system (SAS), an oil-in-water adjuvant, plus Carbopol; high responses (3658–7108) were observed with DS-Cav1 adjuvanted with Alum, SAS alone, Adjuplex, Poly (I:C) and Poly (IC:LC); and moderate responses (1251–2129) were observed with DS-Cav1 adjuvanted with the TLR4 agonist MPLA, Alum plus MPLA or AddaVax. In contrast, DS-Cav1 without adjuvant induced low-level responses (6). A balanced IgG1 and IgG2a (Th2/Th1) immune response was elicited in most of the high to very high response groups (all but Alum and Adjuplex). We also tested the immune response induced by DS-Cav1 in elderly mice with pre-existing DS-Cav1 immunity; we observed that DS-Cav1 adjuvanted with SAS plus Carbopol boosted the response 2-3-fold, whereas DS-Cav1 adjuvanted with alum boosted the response 5-fold. Finally, we tested whether a mixture of ISA 71 VG and Carbopol would enhanced the antibody response in DS-Cav1 immunized calves. While pre-F-stabilized bovine RSV F induced very high titers in mice when adjuvanted with SAS plus Carbopol, the addition of Carbopol to ISA 71 VG did not enhance immune responses in calves. The vaccine response to pre-F-stabilized RSV F is augmented by adjuvant, but the degree of adjuvant-induced enhancement appears to be both context-dependent and species-specific. Public Library of Science 2017-10-26 /pmc/articles/PMC5658087/ /pubmed/29073183 http://dx.doi.org/10.1371/journal.pone.0186854 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Sastry, Mallika
Zhang, Baoshan
Chen, Man
Joyce, M. Gordon
Kong, Wing-Pui
Chuang, Gwo-Yu
Ko, Kiyoon
Kumar, Azad
Silacci, Chiara
Thom, Michelle
Salazar, Andres M.
Corti, Davide
Lanzavecchia, Antonio
Taylor, Geraldine
Mascola, John R.
Graham, Barney S.
Kwong, Peter D.
Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus
title Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus
title_full Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus
title_fullStr Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus
title_full_unstemmed Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus
title_short Adjuvants and the vaccine response to the DS-Cav1-stabilized fusion glycoprotein of respiratory syncytial virus
title_sort adjuvants and the vaccine response to the ds-cav1-stabilized fusion glycoprotein of respiratory syncytial virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658087/
https://www.ncbi.nlm.nih.gov/pubmed/29073183
http://dx.doi.org/10.1371/journal.pone.0186854
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