Show simple item record

dc.contributor.authorWolf, Asia-Sophia Fumika Michaela
dc.contributor.authorHammersbøen, Kristin Reine
dc.contributor.authorØrbo, Hilde Sofie Sager
dc.contributor.authorBhandari, Sabin
dc.contributor.authorSolum, Guri
dc.contributor.authorKjønstad, Ingrid Fadum
dc.contributor.authorJyssum, Ingrid
dc.contributor.authorNygaard, Unni Cecilie
dc.contributor.authorKristoffersen, Anja Bråthen
dc.contributor.authorChristensen, Ingrid Egeland
dc.contributor.authorJosefsson, Sarah Elisabet
dc.contributor.authorLund, Katrine Persgård
dc.contributor.authorChopra, Adity
dc.contributor.authorOsen, Julie Røkke
dc.contributor.authorChaban, Viktoriia
dc.contributor.authorTveter, Anne Therese
dc.contributor.authorSexton, Joseph
dc.contributor.authorKvien, Tore Kristian Aaserud
dc.contributor.authorJahnsen, Jørgen
dc.contributor.authorHaavardsholm, Espen A.
dc.contributor.authorGrødeland, Gunnveig
dc.contributor.authorVaage, John T.
dc.contributor.authorProvan, Sella Aarrestad
dc.contributor.authorKared, Hassen
dc.contributor.authorLund-Johansen, Fridtjof
dc.contributor.authorMunthe, Ludvig Andre
dc.contributor.authorSyversen, Silje Watterdal
dc.contributor.authorGoll, Guro Løvik
dc.contributor.authorJørgensen, Kristin Kaasen
dc.contributor.authorMjaaland, Siri
dc.date.accessioned2025-03-03T13:50:35Z
dc.date.available2025-03-03T13:50:35Z
dc.date.created2024-09-23T09:44:29Z
dc.date.issued2024
dc.identifier.citationEBioMedicine. 2024, 108 .en_US
dc.identifier.issn2352-3964
dc.identifier.urihttps://hdl.handle.net/11250/3181504
dc.description.abstractBackground Understanding cellular responses to SARS-CoV-2 immunisations is important for informing vaccine recommendations in patients with inflammatory bowel disease (IBD) and other vulnerable patients on immunosuppressive therapies. This study investigated the magnitude and quality of T cell responses after multiple SARS-CoV-2 vaccine doses and COVID-19 breakthrough infection. Methods This prospective, observational study included patients with IBD and arthritis on tumour necrosis factor inhibitors (TNFi) receiving up to four SARS-CoV-2 vaccine doses. T cell responses to SARS-CoV-2 peptides were measured by flow cytometry before and 2–4 weeks after vaccinations and breakthrough infection to assess the frequency and polyfunctionality of responding cells, along with receptor-binding domain (anti-RBD) antibodies. Findings Between March 2, 2021, and December 20, 2022, 143 patients (118 IBD, 25 arthritis) and 73 healthy controls were included. In patients with either IBD or arthritis, humoral immunity was attenuated compared to healthy controls (median anti-RBD levels 3391 vs. 6280 BAU/ml, p = 0.008) after three SARS-CoV-2 vaccine doses. Patients with IBD had comparable quantities (median CD4 0.11% vs. 0.11%, p = 0.26, CD8 0.031% vs. 0.047%, p = 0.33) and quality (polyfunctionality score: 0.403 vs. 0.371, p = 0.39; 0.105 vs. 0.101, p = 0.87) of spike-specific T cells to healthy controls. Patients with arthritis had lower frequencies but comparable quality of responding T cells to controls. Breakthrough infection increased spike-specific CD8 T cell quality and T cell responses against non-spike peptides. Interpretation Patients with IBD on TNFi have T cell responses comparable to healthy controls despite attenuated humoral responses following three vaccine doses. Repeated vaccination and breakthrough infection increased the quality of T cell responses. Our study adds evidence that, in the absence of other risk factors, this group may in future be able to follow the general recommendations for COVID-19 vaccines.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleT cell responses to repeated SARS-CoV-2 vaccination and breakthrough infections in patients on TNF inhibitor treatment: a prospective cohort studyen_US
dc.title.alternativeT cell responses to repeated SARS-CoV-2 vaccination and breakthrough infections in patients on TNF inhibitor treatment: a prospective cohort studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber12en_US
dc.source.volume108en_US
dc.source.journalEBioMedicineen_US
dc.identifier.doi10.1016/j.ebiom.2024.105317
dc.identifier.cristin2300403
dc.relation.projectNorges forskningsråd: 332727en_US
dc.relation.projectNorges forskningsråd: 328657en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal