Show simple item record

dc.contributor.author Graham, C.
dc.contributor.author Chooniedass, R.
dc.contributor.author Stefura, W. P
dc.contributor.author Lotoski, L.
dc.contributor.author Lopez, P.
dc.contributor.author Befus, A. D
dc.contributor.author Becker, A. B
dc.contributor.author HayGlass, K. T
dc.date.accessioned 2017-03-06T17:26:51Z
dc.date.available 2017-03-06T17:26:51Z
dc.date.issued 2017-03-02
dc.identifier.citation Journal of Translational Medicine. 2017 Mar 02;15(1):53
dc.identifier.uri http://dx.doi.org/10.1186/s12967-017-1154-3
dc.identifier.uri http://hdl.handle.net/1993/32146
dc.description.abstract Abstract Background Although discovery research has identified the importance of dozens of pro- and anti-inflammatory immune mediators in the pathogenesis, maintenance, exacerbation and resolution of inflammatory diseases, most human cohort studies have incorporated few or no immunological intermediate phenotypes in their analyses. Significant hindrances have been (1) the limited panel of biomarkers known to be readily detected in healthy human populations and (2) the stability, hence utility, of such biomarkers to repeated analysis. Methods The frequency and stability of 14 plasma biomarkers linked to in vivo immune regulation of allergic and autoimmune inflammatory disorders was determined in 140 healthy pediatric and adult participants. The impact of initial and multiple subsequent freeze/thaw cycles on pro-inflammatory (CCL2, CXCL10, IL-18, TNFα, IL-6), anti-inflammatory (IL-10, sTNF-RII, IL-1Ra), acute phase proteins (CRP, PTX3) and other biomarkers (sST2, IL-1RAcP) was subsequently quantified. Results Multiple biomarkers capable of providing an innate immune signature of inflammation were readily detected directly ex vivo in healthy individuals. These biomarker levels were unaffected when comparing paired data sets from freshly obtained, never frozen plasma or serum and matched aliquots despite extensive freeze/thaw cycles. Neither age nor sex affected stability. Similarly, no quantitative differences were found following repetitive analysis of inflammatory biomarkers in culture samples obtained following in vitro stimulation with TLR and RLR ligands. Conclusions A broad panel of in vivo and ex vivo cytokine, chemokine and acute phase protein biomarkers that have been linked to human chronic inflammatory disorders are readily detected in vivo and remain stable for analysis despite multiple freeze thaw cycles. These data provide the foundation and confidence for large scale analyses of panels of inflammatory biomarkers to provide better understanding of immunological mechanisms underlying health versus disease.
dc.title Stability of pro- and anti-inflammatory immune biomarkers for human cohort studies
dc.type Journal Article
dc.language.rfc3066 en
dc.rights.holder The Author(s)
dc.date.updated 2017-03-02T17:03:10Z


Files in this item

This item appears in the following Collection(s)

  • Research Publications [1137]
    This collection contains full text research publications authored or co-authored by University of Manitoba researchers.

Show simple item record

View Statistics