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dc.date.accessioned2019-04-05T08:02:57Z
dc.date.available2019-04-05T08:02:57Z
dc.date.created2019-02-14T22:39:26Z
dc.date.issued2018
dc.identifier.citationGaya de Costa, Mariana Poppelaars, Felix van Kooten, Cees Mollnes, Tom Eirik Tedesco, Francesco Würzner, Reinhard Trouw, Leendert A. Truedsson, Lennart Daha, Mohamed R. Roos, Anja Seelen, Marc A. . Age and Sex-Associated Changes of Complement Activity and Complement Levels in a Healthy Caucasian Population. Frontiers in Immunology. 2018, 9
dc.identifier.urihttp://hdl.handle.net/10852/67570
dc.description.abstractIntroduction: The complement system is essential for an adequate immune response. Much attention has been given to the role of complement in disease. However, to better understand complement in pathology, it is crucial to first analyze this system under different physiological conditions. The aim of the present study was therefore to investigate the inter-individual variation in complement activity and the influences of age and sex. Methods: Complement levels and functional activity were determined in 120 healthy volunteers, 60 women, 60 men, age range 20–69 year. Serum functional activity of the classical pathway (CP), lectin pathway activated by mannan (MBL-LP) and alternative pathway (AP) was measured in sera, using deposition of C5b-9 as readout. In addition, levels of C1q, MBL, MASP-1, MASP-2, ficolin-2, ficolin-3, C2, C4, C3, C5, C6, C7, C8, C9, factor B, factor D, properdin, C1-inhibitor and C4b-binding protein, were determined. Age- and sex-related differences were evaluated. Results: Significantly lower AP activity was found in females compared to males. Further analysis of the AP revealed lower C3 and properdin levels in females, while factor D concentrations were higher. MBL-LP activity was not influenced by sex, but MBL and ficolin-3 levels were significantly lower in females compared to males. There were no significant differences in CP activity or CP components between females and males, nevertheless females had significantly lower levels of the terminal components. The CP and AP activity was significantly higher in the elderly, in contrast to MBL-LP activity. Moreover, C1-inhibitor, C5, C8, and C9 increased with age in contrast to a decrease of factor D and C3 levels. In-depth analysis of the functional activity assays revealed that MBL-LP activity was predominantly dependent on MBL and MASP-2 concentration, whereas CP activity relied on C2, C1-inhibitor and C5 levels. AP activity was strongly and directly associated with levels of C3, factor B and C5. Conclusion: This study demonstrated significant sex and age-related differences in complement levels and functionality in the healthy population. Therefore, age and sex analysis should be taken into consideration when discussing complement-related pathologies and subsequent complement-targeted therapies.en_US
dc.languageEN
dc.publisherFrontiers Research Foundation
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleAge and Sex-Associated Changes of Complement Activity and Complement Levels in a Healthy Caucasian Populationen_US
dc.typeJournal articleen_US
dc.creator.authorGaya de Costa, Mariana
dc.creator.authorPoppelaars, Felix
dc.creator.authorvan Kooten, Cees
dc.creator.authorMollnes, Tom Eirik
dc.creator.authorTedesco, Francesco
dc.creator.authorWürzner, Reinhard
dc.creator.authorTrouw, Leendert A.
dc.creator.authorTruedsson, Lennart
dc.creator.authorDaha, Mohamed R.
dc.creator.authorRoos, Anja
dc.creator.authorSeelen, Marc A.
cristin.unitcode185,53,18,12
cristin.unitnameAvdeling for immunologi og transfusjonsmedisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1677470
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Frontiers in Immunology&rft.volume=9&rft.spage=&rft.date=2018
dc.identifier.jtitleFrontiers in Immunology
dc.identifier.volume9
dc.identifier.doihttp://dx.doi.org/10.3389/fimmu.2018.02664
dc.identifier.urnURN:NBN:no-70754
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1664-3224
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/67570/1/da%2BCosta_Front%2BImmunol_Cristin-post%2B1677470.pdf
dc.type.versionPublishedVersion
cristin.articleid2664
dc.relation.projectNFR/223255


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