Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/37636
Full metadata record
DC FieldValueLanguage
dc.contributor.authorVan Praet, J-
dc.contributor.authorReynders, Marijke-
dc.contributor.authorDe Bacquer, D-
dc.contributor.authorViaene, L-
dc.contributor.authorSCHOUTTETEN, Melanie-
dc.contributor.authorCaluwe, R-
dc.contributor.authorDoubel, P-
dc.contributor.authorHEYLEN, Line-
dc.contributor.authorDe Bel, AV-
dc.contributor.authorVan Vlem, B-
dc.contributor.authorDe Vriese, AS-
dc.contributor.authorSTEENSELS, Deborah-
dc.date.accessioned2022-07-04T12:12:22Z-
dc.date.available2022-07-04T12:12:22Z-
dc.date.issued2021-
dc.date.submitted2022-07-04T07:49:06Z-
dc.identifier.citationJournal of the American Society of Nephrology, 32 (12) , p. 3208 -3220-
dc.identifier.urihttp://hdl.handle.net/1942/37636-
dc.description.abstractBackground Preliminary evidence suggests patients on hemodialysis have a blunted early serological response to SARS-CoV-2 vaccination. Optimizing the vaccination strategy in this population requires a thorough understanding of predictors and dynamics of humoral and cellular immune responses to differentSARS-CoV-2 vaccines.Methods This prospective multicenter study of 543 patients on hemodialysis and 75 healthy volunteers evaluated the immune responses at 4 or 5 weeks and 8 or 9 weeks after administration of the BNT162b2or mRNA-1273 vaccine, respectively. We assessed antiSARS-CoV-2 spike antibodies and T cell responses by IFN-? secretion of peripheral blood lymphocytes upon SARS-CoV-2 glycoprotein stimulation (QuantiFERON assay) and evaluated potential predictors of the responses.Results Compared with healthy volunteers, patients on hemodialysis had an incomplete, delayed humoral immune response and a blunted cellular immune response. Geometric mean antibody titers at both timepoints were significantly greater in patients vaccinated with mRNA-1273 versus BNT162b2, and a larger proportion of them achieved the threshold of 4160 AU/ml, corresponding with high neutralizing antibody titers in vitro(53.6% versus 31.8% at 8 or 9 weeks, P < 0.0001). Patients vaccinated with mRNA-1273 versusBNT162b2 exhibited significantly greater median QuantiFERON responses at both time points, and a larger proportion achieved the threshold of 0.15 IU/ml (64.4% versus 46.9% at 8 or 9 weeks, P < 0.0001).Multivariate analysis identified COVID-19 experience, vaccine type, use of immunosuppressive drugs, serum albumin, lymphocyte count, hepatitis B vaccine nonresponder status, and dialysis vintage as independent predictors of the humoral and cellular responses. <br>Conclusions The mRNA-1273 vaccine's greater immunogenicity may be related to its higher mRNA dose. This suggests a high-dose vaccine might improve the impaired immune response to SARS-CoV-2 vaccination in patients on hemodialysis.-
dc.description.sponsorshipThis research was supported by Amgen (DONATION-331036). A. De Vriese and J. Van Praet designed the study; R. Caluw e, A. De Bel, A. De Vriese, P. Doubel, L. Heylen, M. Schoutteten, J. Van Praet, B. Van Vlem, and L. Viaene provided study materials or patients; D. De Bacquer, A. De Vriese, M. Reynders, and J. Van Praet analyzed the data; D. De Bacquer and J. Van Praet made the figures; A. De Vriese drafted the paper; D. De Bacquer, M. Reynders, and J. Van Praet revised it critically for important intellectual content; all authors approved the final version of the manuscript. The authors are indebted to Tessa Acke, Manuela Caster, Evelyne Deglorie, Mirjam Demesmaecker, Suzanne Driessens, Inne Hoebrekx, Annelien Leunen, Carine Lowis, Isabel Moyaert, Danny Pauwels, Joris Penders, Melissa Renders, Carmen Reynders, Sofie Tombeur, Katrien Uyttersprot, Femke Van Den Berg, Kristel Van Varenbergh, Tine Verheyen, Manon Verhulst, and Sophie Vleeschouwers for their invaluable help in the collection of the patient data and analysis of the samples.-
dc.language.isoen-
dc.publisherAMER SOC NEPHROLOGY-
dc.rights2021 by the American Society of Nephrology-
dc.subject.otherclinical trial-
dc.subject.otherdialysis-
dc.subject.otherSARS-CoV-2-
dc.subject.othervaccination-
dc.subject.otherCOVID-19-
dc.subject.othercellular immunity-
dc.titlePredictors and Dynamics of the Humoral and Cellular Immune Response to SARS-CoV-2 mRNA Vaccines in Hemodialysis Patients: A Multicenter Observational Study-
dc.typeJournal Contribution-
dc.identifier.epage3220-
dc.identifier.issue12-
dc.identifier.spage3208-
dc.identifier.volume32-
local.bibliographicCitation.jcatA1-
local.publisher.place1725 I ST, NW STE 510, WASHINGTON, DC 20006 USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1681/asn.2021070908-
dc.identifier.isi000726153000001-
local.provider.typeWeb of Science-
local.uhasselt.internationalno-
item.validationecoom 2022-
item.contributorVan Praet, J-
item.contributorReynders, Marijke-
item.contributorDe Bacquer, D-
item.contributorViaene, L-
item.contributorSCHOUTTETEN, Melanie-
item.contributorCaluwe, R-
item.contributorDoubel, P-
item.contributorHEYLEN, Line-
item.contributorDe Bel, AV-
item.contributorVan Vlem, B-
item.contributorDe Vriese, AS-
item.contributorSTEENSELS, Deborah-
item.accessRightsOpen Access-
item.fullcitationVan Praet, J; Reynders, Marijke; De Bacquer, D; Viaene, L; SCHOUTTETEN, Melanie; Caluwe, R; Doubel, P; HEYLEN, Line; De Bel, AV; Van Vlem, B; De Vriese, AS & STEENSELS, Deborah (2021) Predictors and Dynamics of the Humoral and Cellular Immune Response to SARS-CoV-2 mRNA Vaccines in Hemodialysis Patients: A Multicenter Observational Study. In: Journal of the American Society of Nephrology, 32 (12) , p. 3208 -3220.-
item.fulltextWith Fulltext-
crisitem.journal.issn1046-6673-
crisitem.journal.eissn1533-3450-
Appears in Collections:Research publications
Files in This Item:
File Description SizeFormat 
ASN.2021070908.pdfPublished version983.68 kBAdobe PDFView/Open
Show simple item record

WEB OF SCIENCETM
Citations

67
checked on May 2, 2024

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.