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Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a

BACKGROUND: We have previously demonstrated that polyfunctional Ty21a-responsive CD4(+) and CD8(+) T cells are generated at the duodenal mucosa 18 days following vaccination with live-attenuated S. Typhi (Ty21a). The longevity of cellular responses has been assessed in peripheral blood, but persiste...

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Autores principales: Pennington, Shaun H., Ferreira, Daniela M., Reiné, Jesús, Nyirenda, Tonney S., Thompson, Ameeka L., Hancock, Carole A., Wright, Angela D., Gordon, Stephen B., Gordon, Melita A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041722/
https://www.ncbi.nlm.nih.gov/pubmed/29958737
http://dx.doi.org/10.1016/j.vaccine.2018.05.114
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author Pennington, Shaun H.
Ferreira, Daniela M.
Reiné, Jesús
Nyirenda, Tonney S.
Thompson, Ameeka L.
Hancock, Carole A.
Wright, Angela D.
Gordon, Stephen B.
Gordon, Melita A.
author_facet Pennington, Shaun H.
Ferreira, Daniela M.
Reiné, Jesús
Nyirenda, Tonney S.
Thompson, Ameeka L.
Hancock, Carole A.
Wright, Angela D.
Gordon, Stephen B.
Gordon, Melita A.
author_sort Pennington, Shaun H.
collection PubMed
description BACKGROUND: We have previously demonstrated that polyfunctional Ty21a-responsive CD4(+) and CD8(+) T cells are generated at the duodenal mucosa 18 days following vaccination with live-attenuated S. Typhi (Ty21a). The longevity of cellular responses has been assessed in peripheral blood, but persistence of duodenal responses is unknown. METHODS: We vaccinated eight healthy adults with Ty21a. Peripheral blood and duodenal samples were acquired after a median of 1.5 years (ranging from 1.1 to 3.7 years) following vaccination. Cellular responses were assessed in peripheral blood and at the duodenal mucosa by flow cytometry. Levels of IgG and IgA were also assessed in peripheral blood by enzyme-linked immunosorbent assay. RESULTS: No T-cell responses were observed at the duodenal mucosa, but CD4(+) T-cell responses to Ty21a and FliC were observed in peripheral blood. Peripheral anti-lipopolysaccharide IgG and IgA responses were also observed. Early immunoglobulin responses were not associated with the persistence of long-term cellular immune responses. CONCLUSIONS: Early T-cell responses which we have previously observed at the duodenal mucosa 18 days following oral vaccination with Ty21a could not be detected at a median of 1.5 years. Peripheral responses were observed at this time. Immunoglobulin responses observed shortly after vaccination were not associated with cellular immune responses at 1.5 years, suggesting that the persistence of cellular immunity is not associated with the strength of the initial humoral response to vaccination.
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spelling pubmed-60417222018-07-25 Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a Pennington, Shaun H. Ferreira, Daniela M. Reiné, Jesús Nyirenda, Tonney S. Thompson, Ameeka L. Hancock, Carole A. Wright, Angela D. Gordon, Stephen B. Gordon, Melita A. Vaccine Article BACKGROUND: We have previously demonstrated that polyfunctional Ty21a-responsive CD4(+) and CD8(+) T cells are generated at the duodenal mucosa 18 days following vaccination with live-attenuated S. Typhi (Ty21a). The longevity of cellular responses has been assessed in peripheral blood, but persistence of duodenal responses is unknown. METHODS: We vaccinated eight healthy adults with Ty21a. Peripheral blood and duodenal samples were acquired after a median of 1.5 years (ranging from 1.1 to 3.7 years) following vaccination. Cellular responses were assessed in peripheral blood and at the duodenal mucosa by flow cytometry. Levels of IgG and IgA were also assessed in peripheral blood by enzyme-linked immunosorbent assay. RESULTS: No T-cell responses were observed at the duodenal mucosa, but CD4(+) T-cell responses to Ty21a and FliC were observed in peripheral blood. Peripheral anti-lipopolysaccharide IgG and IgA responses were also observed. Early immunoglobulin responses were not associated with the persistence of long-term cellular immune responses. CONCLUSIONS: Early T-cell responses which we have previously observed at the duodenal mucosa 18 days following oral vaccination with Ty21a could not be detected at a median of 1.5 years. Peripheral responses were observed at this time. Immunoglobulin responses observed shortly after vaccination were not associated with cellular immune responses at 1.5 years, suggesting that the persistence of cellular immunity is not associated with the strength of the initial humoral response to vaccination. Elsevier Science 2018-07-25 /pmc/articles/PMC6041722/ /pubmed/29958737 http://dx.doi.org/10.1016/j.vaccine.2018.05.114 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pennington, Shaun H.
Ferreira, Daniela M.
Reiné, Jesús
Nyirenda, Tonney S.
Thompson, Ameeka L.
Hancock, Carole A.
Wright, Angela D.
Gordon, Stephen B.
Gordon, Melita A.
Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a
title Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a
title_full Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a
title_fullStr Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a
title_full_unstemmed Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a
title_short Longevity of duodenal and peripheral T-cell and humoral responses to live-attenuated Salmonella Typhi strain Ty21a
title_sort longevity of duodenal and peripheral t-cell and humoral responses to live-attenuated salmonella typhi strain ty21a
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041722/
https://www.ncbi.nlm.nih.gov/pubmed/29958737
http://dx.doi.org/10.1016/j.vaccine.2018.05.114
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