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Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine
BACKGROUND: Toll-like receptor (TLR) agonists reportedly have potent antiviral and antitumor activities and may be a new kind of adjuvant for enhancing immune efficacy. Resiquimod (R848) is an imidazoquinoline compound with potent antiviral activity and functions through the TLR7/TLR8 MyD88-dependen...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892093/ https://www.ncbi.nlm.nih.gov/pubmed/24386990 http://dx.doi.org/10.1186/1746-6148-10-2 |
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author | Zhou, Chun-Xue Li, Dong Chen, Ying-Li Lu, Zeng-Jun Sun, Pu Cao, Yi-Mei Bao, Hui-Fang Fu, Yuan-Fang Li, Ping-Hua Bai, Xing-Wen Xie, Bao-Xia Liu, Zai-Xin |
author_facet | Zhou, Chun-Xue Li, Dong Chen, Ying-Li Lu, Zeng-Jun Sun, Pu Cao, Yi-Mei Bao, Hui-Fang Fu, Yuan-Fang Li, Ping-Hua Bai, Xing-Wen Xie, Bao-Xia Liu, Zai-Xin |
author_sort | Zhou, Chun-Xue |
collection | PubMed |
description | BACKGROUND: Toll-like receptor (TLR) agonists reportedly have potent antiviral and antitumor activities and may be a new kind of adjuvant for enhancing immune efficacy. Resiquimod (R848) is an imidazoquinoline compound with potent antiviral activity and functions through the TLR7/TLR8 MyD88-dependent signaling pathway. Polyinosinic-polycytidylic acid [poly(I:C)] is a synthetic analog of double-stranded RNA that induces the production of pro-inflammatory cytokines by the activation of NF-κB through TLR3. This study investigated the potential of R848 and poly(I:C) as an adjuvant 146S foot-and-mouth disease virus (FMDV) vaccine formulated with aluminum hydroxide (Al(OH)(3)). RESULTS: Antibody titers to FMDV and CD8(+) T cells were markedly enhanced in mice immunized to 146S FMDV + Al(OH)(3) + R848 + poly(I:C) compared with mice immunized to FMDV + ISA206. IFN-γ secretion substantially increased compared with IL-4 secretion by splenic T cells stimulated with FMDV antigens in vitro, suggesting that R848, poly(I:C), and with Al(OH)(3) together biased the immune response toward a Th1-type direction. CONCLUSIONS: These results indicated that the R848 and poly(I:C) together with Al(OH)(3) enhanced humoral and cellular immune responses to immunization with 146S FMDV antigens. Thus, this new vaccine formulation can be used for FMDV prevention. |
format | Online Article Text |
id | pubmed-3892093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38920932014-01-15 Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine Zhou, Chun-Xue Li, Dong Chen, Ying-Li Lu, Zeng-Jun Sun, Pu Cao, Yi-Mei Bao, Hui-Fang Fu, Yuan-Fang Li, Ping-Hua Bai, Xing-Wen Xie, Bao-Xia Liu, Zai-Xin BMC Vet Res Research Article BACKGROUND: Toll-like receptor (TLR) agonists reportedly have potent antiviral and antitumor activities and may be a new kind of adjuvant for enhancing immune efficacy. Resiquimod (R848) is an imidazoquinoline compound with potent antiviral activity and functions through the TLR7/TLR8 MyD88-dependent signaling pathway. Polyinosinic-polycytidylic acid [poly(I:C)] is a synthetic analog of double-stranded RNA that induces the production of pro-inflammatory cytokines by the activation of NF-κB through TLR3. This study investigated the potential of R848 and poly(I:C) as an adjuvant 146S foot-and-mouth disease virus (FMDV) vaccine formulated with aluminum hydroxide (Al(OH)(3)). RESULTS: Antibody titers to FMDV and CD8(+) T cells were markedly enhanced in mice immunized to 146S FMDV + Al(OH)(3) + R848 + poly(I:C) compared with mice immunized to FMDV + ISA206. IFN-γ secretion substantially increased compared with IL-4 secretion by splenic T cells stimulated with FMDV antigens in vitro, suggesting that R848, poly(I:C), and with Al(OH)(3) together biased the immune response toward a Th1-type direction. CONCLUSIONS: These results indicated that the R848 and poly(I:C) together with Al(OH)(3) enhanced humoral and cellular immune responses to immunization with 146S FMDV antigens. Thus, this new vaccine formulation can be used for FMDV prevention. BioMed Central 2014-01-03 /pmc/articles/PMC3892093/ /pubmed/24386990 http://dx.doi.org/10.1186/1746-6148-10-2 Text en Copyright © 2014 Zhou et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhou, Chun-Xue Li, Dong Chen, Ying-Li Lu, Zeng-Jun Sun, Pu Cao, Yi-Mei Bao, Hui-Fang Fu, Yuan-Fang Li, Ping-Hua Bai, Xing-Wen Xie, Bao-Xia Liu, Zai-Xin Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine |
title | Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine |
title_full | Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine |
title_fullStr | Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine |
title_full_unstemmed | Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine |
title_short | Resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine |
title_sort | resiquimod and polyinosinic–polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892093/ https://www.ncbi.nlm.nih.gov/pubmed/24386990 http://dx.doi.org/10.1186/1746-6148-10-2 |
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