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Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin
The skin is an ideal target tissue for vaccine delivery for a number of reasons. It is highly accessible, and most importantly, enriched in professional antigen presenting cells. Possessing strong similarities to human skin physiology and displaying a defined epidermis, the guinea pig is an appropri...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221502/ https://www.ncbi.nlm.nih.gov/pubmed/27894716 http://dx.doi.org/10.1016/j.vaccine.2016.11.052 |
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author | Schultheis, Katherine Schaefer, Hubert Yung, Bryan S. Oh, Janet Muthumani, Karuppiah Humeau, Laurent Broderick, Kate E. Smith, Trevor R.F. |
author_facet | Schultheis, Katherine Schaefer, Hubert Yung, Bryan S. Oh, Janet Muthumani, Karuppiah Humeau, Laurent Broderick, Kate E. Smith, Trevor R.F. |
author_sort | Schultheis, Katherine |
collection | PubMed |
description | The skin is an ideal target tissue for vaccine delivery for a number of reasons. It is highly accessible, and most importantly, enriched in professional antigen presenting cells. Possessing strong similarities to human skin physiology and displaying a defined epidermis, the guinea pig is an appropriate model to study epidermal delivery of vaccine. However, whilst we have characterized the humoral responses in the guinea pig associated with skin vaccine protocols we have yet to investigate the T cell responses. In response to this inadequacy, we developed an IFN-γ ELISpot assay to characterize the cellular immune response in the peripheral blood of guinea pigs. Using a nucleoprotein (NP) influenza pDNA vaccination regimen, we characterized host T cell responses. After delivery of the DNA vaccine to the guinea pig epidermis we detected robust and rapid T cell responses. The levels of IFN-γ spot-forming units averaged approximately 5000 per million cells after two immunizations. These responses were broad in that multiple regions across the NP antigen elicited a T cell response. Interestingly, we identified a number of NP immunodominant T cell epitopes to be conserved across an outbred guinea pig population, a phenomenon which was also observed after immunization with a RSV DNA vaccine. We believe this data enhances our understanding of the cellular immune response elicited to a vaccine in guinea pigs, and globally, will advance the use of this model for vaccine development, especially those targeting skin as a delivery site. |
format | Online Article Text |
id | pubmed-5221502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-52215022017-01-09 Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin Schultheis, Katherine Schaefer, Hubert Yung, Bryan S. Oh, Janet Muthumani, Karuppiah Humeau, Laurent Broderick, Kate E. Smith, Trevor R.F. Vaccine Article The skin is an ideal target tissue for vaccine delivery for a number of reasons. It is highly accessible, and most importantly, enriched in professional antigen presenting cells. Possessing strong similarities to human skin physiology and displaying a defined epidermis, the guinea pig is an appropriate model to study epidermal delivery of vaccine. However, whilst we have characterized the humoral responses in the guinea pig associated with skin vaccine protocols we have yet to investigate the T cell responses. In response to this inadequacy, we developed an IFN-γ ELISpot assay to characterize the cellular immune response in the peripheral blood of guinea pigs. Using a nucleoprotein (NP) influenza pDNA vaccination regimen, we characterized host T cell responses. After delivery of the DNA vaccine to the guinea pig epidermis we detected robust and rapid T cell responses. The levels of IFN-γ spot-forming units averaged approximately 5000 per million cells after two immunizations. These responses were broad in that multiple regions across the NP antigen elicited a T cell response. Interestingly, we identified a number of NP immunodominant T cell epitopes to be conserved across an outbred guinea pig population, a phenomenon which was also observed after immunization with a RSV DNA vaccine. We believe this data enhances our understanding of the cellular immune response elicited to a vaccine in guinea pigs, and globally, will advance the use of this model for vaccine development, especially those targeting skin as a delivery site. 2016-11-25 2017-01-03 /pmc/articles/PMC5221502/ /pubmed/27894716 http://dx.doi.org/10.1016/j.vaccine.2016.11.052 Text en http://creativecommons.org/licenses/by/2.0/ This is an open access article under the CC BY-NC-ND license |
spellingShingle | Article Schultheis, Katherine Schaefer, Hubert Yung, Bryan S. Oh, Janet Muthumani, Karuppiah Humeau, Laurent Broderick, Kate E. Smith, Trevor R.F. Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin |
title | Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin |
title_full | Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin |
title_fullStr | Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin |
title_full_unstemmed | Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin |
title_short | Characterization of guinea pig T cell responses elicited after EP-assisted delivery of DNA vaccines to the skin |
title_sort | characterization of guinea pig t cell responses elicited after ep-assisted delivery of dna vaccines to the skin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221502/ https://www.ncbi.nlm.nih.gov/pubmed/27894716 http://dx.doi.org/10.1016/j.vaccine.2016.11.052 |
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