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Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development

[Image: see text] Cocaine abuse is problematic, directly and indirectly impacting the lives of millions, and yet existing therapies are inadequate and usually ineffective. A cocaine vaccine would be a promising alternative therapeutic option, but efficacy is hampered by variable production of antico...

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Autores principales: Lockner, Jonathan W., Eubanks, Lisa M., Choi, Jennifer L., Lively, Jenny M., Schlosburg, Joel E., Collins, Karen C., Globisch, Daniel, Rosenfeld-Gunn, Robin J., Wilson, Ian A., Janda, Kim D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319694/
https://www.ncbi.nlm.nih.gov/pubmed/25531528
http://dx.doi.org/10.1021/mp500520r
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author Lockner, Jonathan W.
Eubanks, Lisa M.
Choi, Jennifer L.
Lively, Jenny M.
Schlosburg, Joel E.
Collins, Karen C.
Globisch, Daniel
Rosenfeld-Gunn, Robin J.
Wilson, Ian A.
Janda, Kim D.
author_facet Lockner, Jonathan W.
Eubanks, Lisa M.
Choi, Jennifer L.
Lively, Jenny M.
Schlosburg, Joel E.
Collins, Karen C.
Globisch, Daniel
Rosenfeld-Gunn, Robin J.
Wilson, Ian A.
Janda, Kim D.
author_sort Lockner, Jonathan W.
collection PubMed
description [Image: see text] Cocaine abuse is problematic, directly and indirectly impacting the lives of millions, and yet existing therapies are inadequate and usually ineffective. A cocaine vaccine would be a promising alternative therapeutic option, but efficacy is hampered by variable production of anticocaine antibodies. Thus, new tactics and strategies for boosting cocaine vaccine immunogenicity must be explored. Flagellin is a bacterial protein that stimulates the innate immune response via binding to extracellular Toll-like receptor 5 (TLR5) and also via interaction with intracellular NOD-like receptor C4 (NLRC4), leading to production of pro-inflammatory cytokines. Reasoning that flagellin could serve as both carrier and adjuvant, we modified recombinant flagellin protein to display a cocaine hapten termed GNE. The resulting conjugates exhibited dose-dependent stimulation of anti-GNE antibody production. Moreover, when adjuvanted with alum, but not with liposomal MPLA, GNE-FliC was found to be better than our benchmark GNE-KLH. This work represents a new avenue for exploration in the use of hapten-flagellin conjugates to elicit antihapten immune responses.
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spelling pubmed-43196942015-12-22 Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development Lockner, Jonathan W. Eubanks, Lisa M. Choi, Jennifer L. Lively, Jenny M. Schlosburg, Joel E. Collins, Karen C. Globisch, Daniel Rosenfeld-Gunn, Robin J. Wilson, Ian A. Janda, Kim D. Mol Pharm [Image: see text] Cocaine abuse is problematic, directly and indirectly impacting the lives of millions, and yet existing therapies are inadequate and usually ineffective. A cocaine vaccine would be a promising alternative therapeutic option, but efficacy is hampered by variable production of anticocaine antibodies. Thus, new tactics and strategies for boosting cocaine vaccine immunogenicity must be explored. Flagellin is a bacterial protein that stimulates the innate immune response via binding to extracellular Toll-like receptor 5 (TLR5) and also via interaction with intracellular NOD-like receptor C4 (NLRC4), leading to production of pro-inflammatory cytokines. Reasoning that flagellin could serve as both carrier and adjuvant, we modified recombinant flagellin protein to display a cocaine hapten termed GNE. The resulting conjugates exhibited dose-dependent stimulation of anti-GNE antibody production. Moreover, when adjuvanted with alum, but not with liposomal MPLA, GNE-FliC was found to be better than our benchmark GNE-KLH. This work represents a new avenue for exploration in the use of hapten-flagellin conjugates to elicit antihapten immune responses. American Chemical Society 2014-12-22 2015-02-02 /pmc/articles/PMC4319694/ /pubmed/25531528 http://dx.doi.org/10.1021/mp500520r Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Lockner, Jonathan W.
Eubanks, Lisa M.
Choi, Jennifer L.
Lively, Jenny M.
Schlosburg, Joel E.
Collins, Karen C.
Globisch, Daniel
Rosenfeld-Gunn, Robin J.
Wilson, Ian A.
Janda, Kim D.
Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development
title Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development
title_full Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development
title_fullStr Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development
title_full_unstemmed Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development
title_short Flagellin as Carrier and Adjuvant in Cocaine Vaccine Development
title_sort flagellin as carrier and adjuvant in cocaine vaccine development
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319694/
https://www.ncbi.nlm.nih.gov/pubmed/25531528
http://dx.doi.org/10.1021/mp500520r
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