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CD4(+) T cell immunity to Salmonella is transient in the circulation

While Salmonella enterica is seen as an archetypal facultative intracellular bacterial pathogen where protection is mediated by CD4(+) T cells, identifying circulating protective cells has proved very difficult, inhibiting steps to identify key antigen specificities. Exploiting a mouse model of vacc...

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Autores principales: Peres, Newton G., Wang, Nancy, Whitney, Paul, Engel, Sven, Shreenivas, Meghanashree M., Comerford, Ian, Hocking, Dianna M., Erazo, Anna B., Förster, Irmgard, Kupz, Andreas, Gebhardt, Thomas, McColl, Shaun R., McSorley, Stephen J., Bedoui, Sammy, Strugnell, Richard A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568161/
https://www.ncbi.nlm.nih.gov/pubmed/34695149
http://dx.doi.org/10.1371/journal.ppat.1010004
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author Peres, Newton G.
Wang, Nancy
Whitney, Paul
Engel, Sven
Shreenivas, Meghanashree M.
Comerford, Ian
Hocking, Dianna M.
Erazo, Anna B.
Förster, Irmgard
Kupz, Andreas
Gebhardt, Thomas
McColl, Shaun R.
McSorley, Stephen J.
Bedoui, Sammy
Strugnell, Richard A.
author_facet Peres, Newton G.
Wang, Nancy
Whitney, Paul
Engel, Sven
Shreenivas, Meghanashree M.
Comerford, Ian
Hocking, Dianna M.
Erazo, Anna B.
Förster, Irmgard
Kupz, Andreas
Gebhardt, Thomas
McColl, Shaun R.
McSorley, Stephen J.
Bedoui, Sammy
Strugnell, Richard A.
author_sort Peres, Newton G.
collection PubMed
description While Salmonella enterica is seen as an archetypal facultative intracellular bacterial pathogen where protection is mediated by CD4(+) T cells, identifying circulating protective cells has proved very difficult, inhibiting steps to identify key antigen specificities. Exploiting a mouse model of vaccination, we show that the spleens of C57BL/6 mice vaccinated with live-attenuated Salmonella serovar Typhimurium (S. Typhimurium) strains carried a pool of IFN-γ(+) CD4(+) T cells that could adoptively transfer protection, but only transiently. Circulating Salmonella-reactive CD4(+) T cells expressed the liver-homing chemokine receptor CXCR6, accumulated over time in the liver and assumed phenotypic characteristics associated with tissue-associated T cells. Liver memory CD4(+) T cells showed TCR selection bias and their accumulation in the liver could be inhibited by blocking CXCL16. These data showed that the circulation of CD4(+) T cells mediating immunity to Salmonella is limited to a brief window after which Salmonella-specific CD4(+) T cells migrate to peripheral tissues. Our observations highlight the importance of triggering tissue-specific immunity against systemic infections.
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spelling pubmed-85681612021-11-05 CD4(+) T cell immunity to Salmonella is transient in the circulation Peres, Newton G. Wang, Nancy Whitney, Paul Engel, Sven Shreenivas, Meghanashree M. Comerford, Ian Hocking, Dianna M. Erazo, Anna B. Förster, Irmgard Kupz, Andreas Gebhardt, Thomas McColl, Shaun R. McSorley, Stephen J. Bedoui, Sammy Strugnell, Richard A. PLoS Pathog Research Article While Salmonella enterica is seen as an archetypal facultative intracellular bacterial pathogen where protection is mediated by CD4(+) T cells, identifying circulating protective cells has proved very difficult, inhibiting steps to identify key antigen specificities. Exploiting a mouse model of vaccination, we show that the spleens of C57BL/6 mice vaccinated with live-attenuated Salmonella serovar Typhimurium (S. Typhimurium) strains carried a pool of IFN-γ(+) CD4(+) T cells that could adoptively transfer protection, but only transiently. Circulating Salmonella-reactive CD4(+) T cells expressed the liver-homing chemokine receptor CXCR6, accumulated over time in the liver and assumed phenotypic characteristics associated with tissue-associated T cells. Liver memory CD4(+) T cells showed TCR selection bias and their accumulation in the liver could be inhibited by blocking CXCL16. These data showed that the circulation of CD4(+) T cells mediating immunity to Salmonella is limited to a brief window after which Salmonella-specific CD4(+) T cells migrate to peripheral tissues. Our observations highlight the importance of triggering tissue-specific immunity against systemic infections. Public Library of Science 2021-10-25 /pmc/articles/PMC8568161/ /pubmed/34695149 http://dx.doi.org/10.1371/journal.ppat.1010004 Text en © 2021 Peres et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Peres, Newton G.
Wang, Nancy
Whitney, Paul
Engel, Sven
Shreenivas, Meghanashree M.
Comerford, Ian
Hocking, Dianna M.
Erazo, Anna B.
Förster, Irmgard
Kupz, Andreas
Gebhardt, Thomas
McColl, Shaun R.
McSorley, Stephen J.
Bedoui, Sammy
Strugnell, Richard A.
CD4(+) T cell immunity to Salmonella is transient in the circulation
title CD4(+) T cell immunity to Salmonella is transient in the circulation
title_full CD4(+) T cell immunity to Salmonella is transient in the circulation
title_fullStr CD4(+) T cell immunity to Salmonella is transient in the circulation
title_full_unstemmed CD4(+) T cell immunity to Salmonella is transient in the circulation
title_short CD4(+) T cell immunity to Salmonella is transient in the circulation
title_sort cd4(+) t cell immunity to salmonella is transient in the circulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568161/
https://www.ncbi.nlm.nih.gov/pubmed/34695149
http://dx.doi.org/10.1371/journal.ppat.1010004
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