Cellular and humoral response to SARS-CoV-2 vaccine BNT162b2 in adults with Chronic Kidney Disease G4/5Vise andre og tillknytning
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.
2024-09-122024-09-122024-09-18bibliografisk kontrollert