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Cellular and humoral response to SARS-CoV-2 vaccine BNT162b2 in adults with Chronic Kidney Disease G4/5
Örebro universitet, Institutionen för medicinska vetenskaper. Region Örebro län. Department of Infectious Diseases.ORCID-id: 0000-0002-8364-9053
Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Karolinska University Hospital, Stockholm, Sweden; Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Örebro universitet, Institutionen för medicinska vetenskaper. Department of Laboratory Medicine, Clinical Microbiology, Örebro University Hospital, Örebro, Sweden.
Department of Renal Medicine, Danderyd Hospital, Stockholm, Sweden.
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2024 (engelsk)Inngår i: New microbes and new infections, E-ISSN 2052-2975, Vol. 62, artikkel-id 101458Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The mRNA vaccines have proven to be very effective in preventing severe disease and death from SARS-CoV-2 in the general population. However, in patients with chronic kidney disease (CKD) in dialysis or with kidney transplants (KT) the vaccine responses vary, with severe breakthrough infections as a consequence. In this intervention study we investigated the magnitude and quality of the responses to mRNA vaccination administered prior to kidney replacement therapy (KRT). Twenty patients with CKD G4/5 and nine healthy controls were followed for 12 months after receiving two doses of BNT162b2 four weeks apart and a booster dose after 3-6 months. Induction of anti-Spike and anti-RBD IgG in plasma followed the same kinetics in CKD patients and controls, with a trend towards higher titers in controls. In accordance, there was no differences in the establishment of Spike-specific memory B-cells between groups. In contrast, the CKD patients showed lower levels of anti-Spike IgG in saliva and Spike-specific CD8+ + T-cells in blood, possibly influencing the capacity of viral clearance which can contribute to an elevated risk of severe breakthrough infections. In conclusion, we found that CKD patients, despite having a reduced mucosal and cytotoxic immunity to BNT162b2, demonstrated a serological response in plasma similar to healthy controls. This suggests that immunization prior to RRT is efficient and motivated. (EudraCT-nr 2021-000988-68).

sted, utgiver, år, opplag, sider
Elsevier, 2024. Vol. 62, artikkel-id 101458
Emneord [en]
Chronic kidney disease, Kidney failure, COVID-19, SARS-CoV-2, Vaccine
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-115908DOI: 10.1016/j.nmni.2024.101458ISI: 001301481200001PubMedID: 39282145Scopus ID: 2-s2.0-85202014969OAI: oai:DiVA.org:oru-115908DiVA, id: diva2:1897172
Forskningsfinansiär
Swedish Research CouncilSwedish Cancer Society
Merknad

This work was founded by the Swedish research council, Cancer-fonden and Örebro Research committee.

Tilgjengelig fra: 2024-09-12 Laget: 2024-09-12 Sist oppdatert: 2024-09-18bibliografisk kontrollert

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