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AuthorKörper, Sixtendc.contributor.author
AuthorSchrezenmeier, Eva Vanessadc.contributor.author
AuthorRincon-Arevalo, Hectordc.contributor.author
AuthorGrüner, Beatedc.contributor.author
AuthorZickler, Danieldc.contributor.author
AuthorWeiss, Manfreddc.contributor.author
AuthorWiesmann, Thomasdc.contributor.author
AuthorZacharowski, Kaidc.contributor.author
AuthorKalbhenn, Johannesdc.contributor.author
AuthorBentz, Martindc.contributor.author
AuthorDollinger, Matthias M.dc.contributor.author
AuthorPaul, Gregordc.contributor.author
AuthorLepper, Philipp M.dc.contributor.author
AuthorErnst, Lucasdc.contributor.author
AuthorWulf, Hinnerkdc.contributor.author
AuthorZinn, Sebastiandc.contributor.author
AuthorAppl, Thomasdc.contributor.author
AuthorJahrsdörfer, Bernddc.contributor.author
AuthorRojewski, Markusdc.contributor.author
AuthorLotfi, Ramindc.contributor.author
AuthorDörner, Thomasdc.contributor.author
AuthorJungwirth, Bettinadc.contributor.author
AuthorSeifried, Erharddc.contributor.author
AuthorFürst, Danieldc.contributor.author
AuthorSchrezenmeier, Hubertdc.contributor.author
Date of accession2023-06-05T09:22:16Zdc.date.accessioned
Available in OPARU since2023-06-05T09:22:16Zdc.date.available
Date of first publication2022-10-06dc.date.issued
AbstractObjectives To determine the profile of cytokines in patients with severe COVID-19 who were enrolled in a trial of COVID-19 convalescent plasma (CCP). Methods Patients were randomized to receive standard treatment and 3 CCP units or standard treatment alone (CAPSID trial, ClinicalTrials.gov NCT04433910). The primary outcome was a dichotomous composite outcome (survival and no longer severe COVID-19 on day 21). Time to clinical improvement was a key secondary endpoint. The concentrations of 27 cytokines were measured (baseline, day 7). We analyzed the change and the correlation between serum cytokine levels over time in different subgroups and the prediction of outcome in receiver operating characteristics (ROC) analyses and in multivariate models. Results The majority of cytokines showed significant changes from baseline to day 7. Some were strongly correlated amongst each other (at baseline the cluster IL-1ß, IL-2, IL-6, IL-8, G-CSF, MIP-1α, the cluster PDGF-BB, RANTES or the cluster IL-4, IL-17, Eotaxin, bFGF, TNF-α). The correlation matrix substantially changed from baseline to day 7. The heatmaps of the absolute values of the correlation matrix indicated an association of CCP treatment and clinical outcome with the cytokine pattern. Low levels of IP-10, IFN-γ, MCP-1 and IL-1ß on day 0 were predictive of treatment success in a ROC analysis. In multivariate models, low levels of IL-1ß, IFN-γ and MCP-1 on day 0 were significantly associated with both treatment success and shorter time to clinical improvement. Low levels of IP-10, IL-1RA, IL-6, MCP-1 and IFN-γ on day 7 and high levels of IL-9, PDGF and RANTES on day 7 were predictive of treatment success in ROC analyses. Low levels of IP-10, MCP-1 and high levels of RANTES, on day 7 were associated with both treatment success and shorter time to clinical improvement in multivariate models. Conclusion This analysis demonstrates a considerable dynamic of cytokines over time, which is influenced by both treatment and clinical course of COVID-19. Levels of IL-1ß and MCP-1 at baseline and MCP-1, IP-10 and RANTES on day 7 were associated with a favorable outcome across several endpoints. These cytokines should be included in future trials for further evaluation as predictive factors.dc.description.abstract
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
LicenseCC BY 4.0 Internationaldc.rights
Link to license texthttps://creativecommons.org/licenses/by/4.0/dc.rights.uri
Keywordconvalescent plasmadc.subject
Keywordpredictive factorsdc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
MeSHCOVID-19; Therapydc.subject.mesh
MeSHChemokinesdc.subject.mesh
MeSHInterleukinsdc.subject.mesh
MeSHRandomized controlled trials as topicdc.subject.mesh
TitleCytokine levels associated with favorable clinical outcome in the CAPSID randomized trial of convalescent plasma in patients with severe COVID-19dc.title
Resource typeWissenschaftlicher Artikeldc.type
SWORD Date2022-10-20T10:48:12Zdc.date.updated
VersionpublishedVersiondc.description.version
DOIhttp://dx.doi.org/10.18725/OPARU-48916dc.identifier.doi
URNhttp://nbn-resolving.de/urn:nbn:de:bsz:289-oparu-48992-5dc.identifier.urn
GNDCOVID-19dc.subject.gnd
GNDTherapiedc.subject.gnd
GNDChemokinedc.subject.gnd
GNDInterleukinedc.subject.gnd
GNDTherapieerfolgdc.subject.gnd
InstitutionInstitut für Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH (IKT)uulm.affiliationSpecific
InstitutionUKU. Institut für Transfusionsmedizinuulm.affiliationSpecific
InstitutionUKU. Klinik für Innere Medizin IIIuulm.affiliationSpecific
InstitutionUKU. Klinik für Anästhesiologie und Intensivmedizinuulm.affiliationSpecific
Peer reviewjauulm.peerReview
DCMI TypeCollectionuulm.typeDCMI
CategoryPublikationenuulm.category
DOI of original publication10.3389/fimmu.2022.1008438dc.relation1.doi
Source - Title of sourceFrontiers in Immunologysource.title
Source - Place of publicationFrontiers Mediasource.publisher
Source - Volume13source.volume
Source - Year2022source.year
Source - Article number1008438source.articleNumber
Source - eISSN1664-3224source.identifier.eissn
Open Accessgold, Green Publisheduulm.OA
WoS000874555800001uulm.identifier.wos
Bibliographyuulmuulm.bibliographie
Project uulmCAPSID / CAPSID „Eine randomisierte, prospektive, offene klinische Studie mit Rekonvaleszenten-Plasma im Vergleich zur bestmöglichen Standardbehandlung von Patientinnen und Patienten mit schwerer COVID-19 Erkrankung“ / BMG / ZMVI1-2520COR802uulm.projectOther


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