Activation of CD4 and CD8 T cell receptors and regulatory T cells in response to human proteins

dc.contributor.authorArneth, Borros M.
dc.date.accessioned2022-11-18T09:55:26Z
dc.date.available2020-08-18T13:36:33Z
dc.date.available2022-11-18T09:55:26Z
dc.date.issued2018
dc.description.abstractThis study assessed in detail the influence of four different human proteins on the activation of CD4+ and CD8+ T lymphocytes and on the formation of regulatory T cells. Human whole-blood samples were incubated with four different human proteins. The effects of these proteins on the downstream immune-system response, on the expression of extracellular activation markers on and intracellular cytokines in T lymphocytes, and on the number of regulatory T cells (T-reg cells) were investigated via flow cytometry. Incubation with beta-actin or glyceraldehyde 3-phosphate dehydrogenase (GAPDH), which are cytoplasmic proteins, increased the expression of both extra-cellular activation markers (CD69 and HLA-DR) and intracellular cytokines but did not significantly affect the number of T-reg cells. In contrast, incubation with human albumin or insulin, which are serum proteins, reduced both extracellular activation markers and intracellular cytokine expression and subsequently increased the number of T-reg cells. These findings may help to explain the etiological basis of autoimmune diseases.en
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:hebis:26-opus-153971
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/9574
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-8962
dc.language.isoende_DE
dc.rightsNamensnennung 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectregulatory T cellsen
dc.subjectCD4+ T helper cellsen
dc.subjectlymphocytesen
dc.subjectCD8+ cytotoxic T cellsen
dc.subjectinterferon-gammaen
dc.subject.ddcddc:610de_DE
dc.titleActivation of CD4 and CD8 T cell receptors and regulatory T cells in response to human proteinsen
dc.typearticlede_DE
local.affiliationFB 11 - Medizinde_DE
local.opus.fachgebietMedizinde_DE
local.opus.id15397
local.opus.instituteInstitute of Laboratory Medicine and Pathobiochemistry, Molecular Diagnosticsde_DE
local.source.freetextPeerJ 6:e4462de_DE
local.source.urihttps://doi.org/10.7717/peerj.4462

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