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DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant

Several agonists to CD40 have shown to induce acquired immune responses. Here, we developed and evaluated the rolling circle amplification (RCA) products that are based on anti-CD40 DNA aptamers as a novel vaccine adjuvant. First, we developed DNA aptamers with specific binding affinity to chicken C...

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Autores principales: Al-Ogaili, Adil S., Liyanage, Rohana, Lay, Jack O., Jiang, Tieshan, Vuong, Christine N., Agrawal, Shilpi, Kumar, Thallapuranam Krishnaswamy Suresh, Berghman, Luc R., Hargis, Billy M., Kwon, Young Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747709/
https://www.ncbi.nlm.nih.gov/pubmed/33335251
http://dx.doi.org/10.1038/s41598-020-79420-w
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author Al-Ogaili, Adil S.
Liyanage, Rohana
Lay, Jack O.
Jiang, Tieshan
Vuong, Christine N.
Agrawal, Shilpi
Kumar, Thallapuranam Krishnaswamy Suresh
Berghman, Luc R.
Hargis, Billy M.
Kwon, Young Min
author_facet Al-Ogaili, Adil S.
Liyanage, Rohana
Lay, Jack O.
Jiang, Tieshan
Vuong, Christine N.
Agrawal, Shilpi
Kumar, Thallapuranam Krishnaswamy Suresh
Berghman, Luc R.
Hargis, Billy M.
Kwon, Young Min
author_sort Al-Ogaili, Adil S.
collection PubMed
description Several agonists to CD40 have shown to induce acquired immune responses. Here, we developed and evaluated the rolling circle amplification (RCA) products that are based on anti-CD40 DNA aptamers as a novel vaccine adjuvant. First, we developed DNA aptamers with specific binding affinity to chicken CD40 extra domain (chCD40ED). Next, we prepared the RCA products that consist of these aptamers to increase the spanning space and overall binding affinity to chCD40ED. Using 8 DNA aptamer candidates, 4 aptamer-based RCA products (aptamer RCAs) were generated, each consisting of two distinct aptamers. We demonstrated that all 4 aptamer RCAs significantly induced the signal transduction in chicken HD11 macrophage cell line (p < 0.05). Finally, we conjugated one of the aptamer RCAs (Aptamer RCA II) to M2e epitope peptide of influenza virus as a model hapten, and the immune complex was injected to chickens. Aptamer RCA II stimulated anti-M2e IgG antibody production to the level significantly higher as compared to the control (M2e epitope alone; p < 0.05). The results of our work suggest that aptamer RCA is a novel platform to boost the efficacy of vaccines, which might find broad applications to other antigens beyond M2e epitope evaluated in this study using chicken infection model.
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spelling pubmed-77477092020-12-22 DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant Al-Ogaili, Adil S. Liyanage, Rohana Lay, Jack O. Jiang, Tieshan Vuong, Christine N. Agrawal, Shilpi Kumar, Thallapuranam Krishnaswamy Suresh Berghman, Luc R. Hargis, Billy M. Kwon, Young Min Sci Rep Article Several agonists to CD40 have shown to induce acquired immune responses. Here, we developed and evaluated the rolling circle amplification (RCA) products that are based on anti-CD40 DNA aptamers as a novel vaccine adjuvant. First, we developed DNA aptamers with specific binding affinity to chicken CD40 extra domain (chCD40ED). Next, we prepared the RCA products that consist of these aptamers to increase the spanning space and overall binding affinity to chCD40ED. Using 8 DNA aptamer candidates, 4 aptamer-based RCA products (aptamer RCAs) were generated, each consisting of two distinct aptamers. We demonstrated that all 4 aptamer RCAs significantly induced the signal transduction in chicken HD11 macrophage cell line (p < 0.05). Finally, we conjugated one of the aptamer RCAs (Aptamer RCA II) to M2e epitope peptide of influenza virus as a model hapten, and the immune complex was injected to chickens. Aptamer RCA II stimulated anti-M2e IgG antibody production to the level significantly higher as compared to the control (M2e epitope alone; p < 0.05). The results of our work suggest that aptamer RCA is a novel platform to boost the efficacy of vaccines, which might find broad applications to other antigens beyond M2e epitope evaluated in this study using chicken infection model. Nature Publishing Group UK 2020-12-17 /pmc/articles/PMC7747709/ /pubmed/33335251 http://dx.doi.org/10.1038/s41598-020-79420-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Al-Ogaili, Adil S.
Liyanage, Rohana
Lay, Jack O.
Jiang, Tieshan
Vuong, Christine N.
Agrawal, Shilpi
Kumar, Thallapuranam Krishnaswamy Suresh
Berghman, Luc R.
Hargis, Billy M.
Kwon, Young Min
DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant
title DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant
title_full DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant
title_fullStr DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant
title_full_unstemmed DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant
title_short DNA aptamer-based rolling circle amplification product as a novel immunological adjuvant
title_sort dna aptamer-based rolling circle amplification product as a novel immunological adjuvant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747709/
https://www.ncbi.nlm.nih.gov/pubmed/33335251
http://dx.doi.org/10.1038/s41598-020-79420-w
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