Publication:
CD154 Expression Indicates T Cell Activation Following Tetanus Toxoid Vaccination of Horses.

cris.virtual.author-orcid0000-0003-1284-4350
cris.virtualsource.author-orcid0393b3fa-fb66-4674-8370-4ea706c7acff
datacite.rightsopen.access
dc.contributor.authorSchnabel, Christiane L
dc.contributor.authorFletemeyer, Babette
dc.contributor.authorLübke, Sabrina
dc.contributor.authorMarti, Eliane Isabelle
dc.contributor.authorWagner, Bettina
dc.contributor.authorAlber, Gottfried
dc.date.accessioned2024-10-09T17:36:12Z
dc.date.available2024-10-09T17:36:12Z
dc.date.issued2022-04-13
dc.description.abstractDespite the relevance of adaptive immunity against equine pathogens antigen-specific T cell responses of horses are not well characterized and the lack of insight into T cell responses hampers the understanding of the pathogeneses of important diseases. In this study we used tetanus toxoid (TT) as a well-defined antigen to characterize antigen-reactive T cells. Six healthy adult horses received a routine booster against tetanus with an immune stimulating complex (ISCOM)-based vaccine and were followed for 28 days. TT-specific serum antibodies were quantified by ELISA and increased in all horses by day 7 after vaccination. CD154 is an established indicator of antigen-reactive T helper cells in other species, but has not been characterized in horses. CD154 detection in equine PBMC by an anti-human CD154 antibody (clone 5C8) was confirmed by Western blots and then applied for flow cytometry. As a common indicator of equine T cell activation, cytokine induction was studied in parallel. T cells were analyzed by multicolor flow cytometry of PBMC after re-stimulation with TT in vitro. Reactive T helper (Th) cells were characterized by increased frequencies of CD4+CD154+ lymphocytes in in vitro TT-re-stimulated PBMC on day 14 after vaccination of the horses compared to pre-vaccination. The majority of all CD154+ cells after TT re-stimulation were CD4+ Th cells, but CD154 was also induced on CD4- cells albeit in lower frequencies. CD154+CD4+ Th cells were enriched in cytokine-expressing cells compared to CD154-CD4+ Th cells. Similar to the CD4+CD154+ frequencies, CD4+IL-4+, CD4+IFN-γ+ and CD4+TNF-α+ were increased after vaccination, but IL-4+ increased later than IFN-γ+ and CD4+TNF-α+, which already exceeded pre-vaccination frequencies on day 7. CD4+CD154+ frequencies correlated positively with those of CD4+IL-4+ (Th2) on day 14, and negatively with CD4+IFN-γ+ induction on day 7, but did not correlate with CD4+TNF-α+ frequencies or TT-specific antibody concentrations. CD154 appears to be a useful marker of antigen-reactive equine Th cells in combination with cytokine expression. The T cell analyses established here with TT can be applied to other antigens relevant for infections or allergies of horses and in horse models for translational research.
dc.description.sponsorshipDepartment of Clinical Research and Veterinary Public Health, Neurologische Wissenschaften
dc.identifier.doi10.48350/169698
dc.identifier.pmid35493462
dc.identifier.publisherDOI10.3389/fimmu.2022.805026
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/70523
dc.language.isoen
dc.publisherFrontiers Research Foundation
dc.relation.ispartofFrontiers in immunology
dc.relation.issn1664-3224
dc.relation.organizationDCD5A442C05DE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C48FE17DE0405C82790C4DE2
dc.subjectCD40 ligand CD40L TRAP antigen-specific equine gp39
dc.subject.ddc600 - Technology::630 - Agriculture
dc.titleCD154 Expression Indicates T Cell Activation Following Tetanus Toxoid Vaccination of Horses.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue805026
oaire.citation.startPage805026
oaire.citation.volume13
oairecerif.author.affiliationDepartment of Clinical Research and Veterinary Public Health, Neurologische Wissenschaften
unibe.contributor.rolecreator
unibe.contributor.rolecreator
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unibe.contributor.rolecreator
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unibe.date.licenseChanged2022-05-04 16:15:20
unibe.description.ispublishedpub
unibe.eprints.legacyId169698
unibe.journal.abbrevTitleFront Immunol
unibe.refereedtrue
unibe.subtype.articlejournal

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