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Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever
The mechanisms by which oral, live-attenuated vaccines protect against typhoid fever are poorly understood. Here, we analyze transcriptional responses after vaccination with Ty21a or vaccine candidate, M01ZH09. Alterations in response profiles were related to vaccine-induced immune responses and sub...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643418/ https://www.ncbi.nlm.nih.gov/pubmed/29075261 http://dx.doi.org/10.3389/fimmu.2017.01276 |
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author | Blohmke, Christoph J. Hill, Jennifer Darton, Thomas C. Carvalho-Burger, Matheus Eustace, Andrew Jones, Claire Schreiber, Fernanda Goodier, Martin R. Dougan, Gordon Nakaya, Helder I. Pollard, Andrew J. |
author_facet | Blohmke, Christoph J. Hill, Jennifer Darton, Thomas C. Carvalho-Burger, Matheus Eustace, Andrew Jones, Claire Schreiber, Fernanda Goodier, Martin R. Dougan, Gordon Nakaya, Helder I. Pollard, Andrew J. |
author_sort | Blohmke, Christoph J. |
collection | PubMed |
description | The mechanisms by which oral, live-attenuated vaccines protect against typhoid fever are poorly understood. Here, we analyze transcriptional responses after vaccination with Ty21a or vaccine candidate, M01ZH09. Alterations in response profiles were related to vaccine-induced immune responses and subsequent outcome after wild-type Salmonella Typhi challenge. Despite broad genetic similarity, we detected differences in transcriptional responses to each vaccine. Seven days after M01ZH09 vaccination, marked cell cycle activation was identified and associated with humoral immunogenicity. By contrast, vaccination with Ty21a was associated with NK cell activity and validated in peripheral blood mononuclear cell stimulation assays confirming superior induction of an NK cell response. Moreover, transcriptional signatures of amino acid metabolism in Ty21a recipients were associated with protection against infection, including increased incubation time and decreased severity. Our data provide detailed insight into molecular immune responses to typhoid vaccines, which could aid the rational design of improved oral, live-attenuated vaccines against enteric pathogens. |
format | Online Article Text |
id | pubmed-5643418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56434182017-10-26 Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever Blohmke, Christoph J. Hill, Jennifer Darton, Thomas C. Carvalho-Burger, Matheus Eustace, Andrew Jones, Claire Schreiber, Fernanda Goodier, Martin R. Dougan, Gordon Nakaya, Helder I. Pollard, Andrew J. Front Immunol Immunology The mechanisms by which oral, live-attenuated vaccines protect against typhoid fever are poorly understood. Here, we analyze transcriptional responses after vaccination with Ty21a or vaccine candidate, M01ZH09. Alterations in response profiles were related to vaccine-induced immune responses and subsequent outcome after wild-type Salmonella Typhi challenge. Despite broad genetic similarity, we detected differences in transcriptional responses to each vaccine. Seven days after M01ZH09 vaccination, marked cell cycle activation was identified and associated with humoral immunogenicity. By contrast, vaccination with Ty21a was associated with NK cell activity and validated in peripheral blood mononuclear cell stimulation assays confirming superior induction of an NK cell response. Moreover, transcriptional signatures of amino acid metabolism in Ty21a recipients were associated with protection against infection, including increased incubation time and decreased severity. Our data provide detailed insight into molecular immune responses to typhoid vaccines, which could aid the rational design of improved oral, live-attenuated vaccines against enteric pathogens. Frontiers Media S.A. 2017-10-12 /pmc/articles/PMC5643418/ /pubmed/29075261 http://dx.doi.org/10.3389/fimmu.2017.01276 Text en Copyright © 2017 Blohmke, Hill, Darton, Carvalho-Burger, Eustace, Jones, Schreiber, Goodier, Dougan, Nakaya and Pollard. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Blohmke, Christoph J. Hill, Jennifer Darton, Thomas C. Carvalho-Burger, Matheus Eustace, Andrew Jones, Claire Schreiber, Fernanda Goodier, Martin R. Dougan, Gordon Nakaya, Helder I. Pollard, Andrew J. Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever |
title | Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever |
title_full | Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever |
title_fullStr | Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever |
title_full_unstemmed | Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever |
title_short | Induction of Cell Cycle and NK Cell Responses by Live-Attenuated Oral Vaccines against Typhoid Fever |
title_sort | induction of cell cycle and nk cell responses by live-attenuated oral vaccines against typhoid fever |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643418/ https://www.ncbi.nlm.nih.gov/pubmed/29075261 http://dx.doi.org/10.3389/fimmu.2017.01276 |
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