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Extracellular vesicles elicit protective immune responses against Salmonella infection
Small extracellular vesicles (sEVs) produced by antigen‐presenting cells represent a novel mechanism of cell‐to‐cell communication. The sEVs have been shown to drive Th1‐type adaptive immune responses against intracellular infections such as Salmonella. In this study, we have demonstrated that an ad...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494607/ https://www.ncbi.nlm.nih.gov/pubmed/36134734 http://dx.doi.org/10.1002/jev2.12267 |
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author | Emerson, Lisa E Barker, Hailey Tran, Terri Barker, Samantha Enslow, Samantha Ou, Mark Hoffman, Carol Jones, Melissa Pascual, David W. Edelmann, Mariola J. |
author_facet | Emerson, Lisa E Barker, Hailey Tran, Terri Barker, Samantha Enslow, Samantha Ou, Mark Hoffman, Carol Jones, Melissa Pascual, David W. Edelmann, Mariola J. |
author_sort | Emerson, Lisa E |
collection | PubMed |
description | Small extracellular vesicles (sEVs) produced by antigen‐presenting cells represent a novel mechanism of cell‐to‐cell communication. The sEVs have been shown to drive Th1‐type adaptive immune responses against intracellular infections such as Salmonella. In this study, we have demonstrated that an administration of sEVs produced by Salmonella‐infected macrophages to BALB/c mice that were then challenged with Salmonella infection decreased bacterial load in infected animals and led to protection against a lethal dose of Salmonella. Second, the same sEVs induced a robust production of IgA anti‐Salmonella antibodies (Abs) in BALB/c mice, including IgA anti‐OmpD Abs. These results show that the nanoscale sEVs stimulate adaptive immune responses against intracellular pathogens and that these sEVs can be used to provide animals with complete protection against lethal infection, such as the systemic bacterial infection in immunodeficient BALB/c mice. |
format | Online Article Text |
id | pubmed-9494607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94946072022-09-30 Extracellular vesicles elicit protective immune responses against Salmonella infection Emerson, Lisa E Barker, Hailey Tran, Terri Barker, Samantha Enslow, Samantha Ou, Mark Hoffman, Carol Jones, Melissa Pascual, David W. Edelmann, Mariola J. J Extracell Vesicles Short Communication Small extracellular vesicles (sEVs) produced by antigen‐presenting cells represent a novel mechanism of cell‐to‐cell communication. The sEVs have been shown to drive Th1‐type adaptive immune responses against intracellular infections such as Salmonella. In this study, we have demonstrated that an administration of sEVs produced by Salmonella‐infected macrophages to BALB/c mice that were then challenged with Salmonella infection decreased bacterial load in infected animals and led to protection against a lethal dose of Salmonella. Second, the same sEVs induced a robust production of IgA anti‐Salmonella antibodies (Abs) in BALB/c mice, including IgA anti‐OmpD Abs. These results show that the nanoscale sEVs stimulate adaptive immune responses against intracellular pathogens and that these sEVs can be used to provide animals with complete protection against lethal infection, such as the systemic bacterial infection in immunodeficient BALB/c mice. John Wiley and Sons Inc. 2022-09-22 2022-09 /pmc/articles/PMC9494607/ /pubmed/36134734 http://dx.doi.org/10.1002/jev2.12267 Text en © 2022 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Short Communication Emerson, Lisa E Barker, Hailey Tran, Terri Barker, Samantha Enslow, Samantha Ou, Mark Hoffman, Carol Jones, Melissa Pascual, David W. Edelmann, Mariola J. Extracellular vesicles elicit protective immune responses against Salmonella infection |
title | Extracellular vesicles elicit protective immune responses against Salmonella infection |
title_full | Extracellular vesicles elicit protective immune responses against Salmonella infection |
title_fullStr | Extracellular vesicles elicit protective immune responses against Salmonella infection |
title_full_unstemmed | Extracellular vesicles elicit protective immune responses against Salmonella infection |
title_short | Extracellular vesicles elicit protective immune responses against Salmonella infection |
title_sort | extracellular vesicles elicit protective immune responses against salmonella infection |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494607/ https://www.ncbi.nlm.nih.gov/pubmed/36134734 http://dx.doi.org/10.1002/jev2.12267 |
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