Human immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.

H. pylori persists in the human stomach over decades and promotes several adverse clinical sequelae including gastritis, peptic ulcers and gastric cancer that are linked to the induction and subsequent evasion of chronic gastric inflammation. Emerging evidence indicates that H. pylori infection may...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Songhua Zhang, Joseph Desrosiers, Jose R Aponte-Pieras, Kristen DaSilva, Loren D Fast, Frances Terry, William D Martin, Anne S De Groot, Leonard Moise, Steven F Moss
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
Materias:
R
Q
Acceso en línea:https://doaj.org/article/b80b2646660e446ebd452d9e27806748
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:b80b2646660e446ebd452d9e27806748
record_format dspace
spelling oai:doaj.org-article:b80b2646660e446ebd452d9e278067482021-11-18T08:22:59ZHuman immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.1932-620310.1371/journal.pone.0094974https://doaj.org/article/b80b2646660e446ebd452d9e278067482014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24740005/?tool=EBIhttps://doaj.org/toc/1932-6203H. pylori persists in the human stomach over decades and promotes several adverse clinical sequelae including gastritis, peptic ulcers and gastric cancer that are linked to the induction and subsequent evasion of chronic gastric inflammation. Emerging evidence indicates that H. pylori infection may also protect against asthma and some other immune-mediated conditions through regulatory T cell effects outside the stomach. To characterize the complexity of the CD4+ T cell response generated during H. pylori infection, computational methods were previously used to generate a panel of 90 predicted epitopes conserved among H. pylori genomes that broadly cover HLA Class II diversity for maximum population coverage. Here, these sequences were tested individually for their ability to induce in vitro responses in peripheral blood mononuclear cells by interferon-γ ELISpot assay. The average number of spot-forming cells/million PBMCs was significantly elevated in H. pylori-infected subjects over uninfected persons. Ten of the 90 peptides stimulated IFN-γ secretion in the H. pylori-infected group only, whereas two out of the 90 peptides elicited a detectable IFN-γ response in the H. pylori-uninfected subjects but no response in the H. pylori-infected group. Cytokine ELISA measurements performed using in vitro PBMC culture supernatants demonstrated significantly higher levels of TNF-α, IL-2, IL-4, IL-6, IL-10, and TGF-β1 in the H. pylori-infected subjects, whereas IL-17A expression was not related to the subjects H. pylori-infection status. Our results indicate that the human T cell responses to these 90 peptides are generally increased in actively H. pylori-infected, compared with H. pylori-naïve, subjects. This information will improve understanding of the complex immune response to H. pylori, aiding rational epitope-driven vaccine design as well as helping identify other H. pylori epitopes with potentially immunoregulatory effects.Songhua ZhangJoseph DesrosiersJose R Aponte-PierasKristen DaSilvaLoren D FastFrances TerryWilliam D MartinAnne S De GrootLeonard MoiseSteven F MossPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 4, p e94974 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Songhua Zhang
Joseph Desrosiers
Jose R Aponte-Pieras
Kristen DaSilva
Loren D Fast
Frances Terry
William D Martin
Anne S De Groot
Leonard Moise
Steven F Moss
Human immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.
description H. pylori persists in the human stomach over decades and promotes several adverse clinical sequelae including gastritis, peptic ulcers and gastric cancer that are linked to the induction and subsequent evasion of chronic gastric inflammation. Emerging evidence indicates that H. pylori infection may also protect against asthma and some other immune-mediated conditions through regulatory T cell effects outside the stomach. To characterize the complexity of the CD4+ T cell response generated during H. pylori infection, computational methods were previously used to generate a panel of 90 predicted epitopes conserved among H. pylori genomes that broadly cover HLA Class II diversity for maximum population coverage. Here, these sequences were tested individually for their ability to induce in vitro responses in peripheral blood mononuclear cells by interferon-γ ELISpot assay. The average number of spot-forming cells/million PBMCs was significantly elevated in H. pylori-infected subjects over uninfected persons. Ten of the 90 peptides stimulated IFN-γ secretion in the H. pylori-infected group only, whereas two out of the 90 peptides elicited a detectable IFN-γ response in the H. pylori-uninfected subjects but no response in the H. pylori-infected group. Cytokine ELISA measurements performed using in vitro PBMC culture supernatants demonstrated significantly higher levels of TNF-α, IL-2, IL-4, IL-6, IL-10, and TGF-β1 in the H. pylori-infected subjects, whereas IL-17A expression was not related to the subjects H. pylori-infection status. Our results indicate that the human T cell responses to these 90 peptides are generally increased in actively H. pylori-infected, compared with H. pylori-naïve, subjects. This information will improve understanding of the complex immune response to H. pylori, aiding rational epitope-driven vaccine design as well as helping identify other H. pylori epitopes with potentially immunoregulatory effects.
format article
author Songhua Zhang
Joseph Desrosiers
Jose R Aponte-Pieras
Kristen DaSilva
Loren D Fast
Frances Terry
William D Martin
Anne S De Groot
Leonard Moise
Steven F Moss
author_facet Songhua Zhang
Joseph Desrosiers
Jose R Aponte-Pieras
Kristen DaSilva
Loren D Fast
Frances Terry
William D Martin
Anne S De Groot
Leonard Moise
Steven F Moss
author_sort Songhua Zhang
title Human immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.
title_short Human immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.
title_full Human immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.
title_fullStr Human immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.
title_full_unstemmed Human immune responses to H. pylori HLA Class II epitopes identified by immunoinformatic methods.
title_sort human immune responses to h. pylori hla class ii epitopes identified by immunoinformatic methods.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/b80b2646660e446ebd452d9e27806748
work_keys_str_mv AT songhuazhang humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT josephdesrosiers humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT joserapontepieras humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT kristendasilva humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT lorendfast humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT francesterry humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT williamdmartin humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT annesdegroot humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT leonardmoise humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
AT stevenfmoss humanimmuneresponsestohpylorihlaclassiiepitopesidentifiedbyimmunoinformaticmethods
_version_ 1718421884139208704