Artykuł w czasopiśmie
Ładowanie...
Miniatura
Licencja

CC-BY-NCCC-BY-NC - Uznanie autorstwa - Użycie niekomercyjne

COVID-19 mRNA BNT162b2 vaccine safety and B-cell and T-cell reactogenicity among children with a history of paediatric multisystem inflammatory syndrome temporally associated with COVID-19 (PIMS-TS) - preliminary study

Autor
Matkowska-Kocjan Agnieszka
Wójcik Marta
Szenborn Filip
Wielgos Katarzyna
Ludwikowska Kamila
Popiel Aneta
Olbromski Mateusz
Biela Mateusz
Zaryczański Janusz
Punktacja ministerialna
200
Data publikacji
Abstrakt (EN)

To assess the safety of Pfizer-BioNTech COVID-19 mRNA BNT162b2 vaccine (Comirnaty®) among patients with the anamnesis of paediatric inflammatory syndrome temporally associated with COVID-19 (PIMS-TS), we conducted a prospective cohort study of 21 patients with history of PIMS (PIMS group, median age 7.4 years, 71% male) and 71 healthy controls without such an anamnesis (CONTROL group, median age 9.0 years, 39% male) aged 5–18 years. Among them, 85 patients (all PIMS patients and 64 CONTROL patients) completed the two dose schedule of vaccination administered 21 days apart and 7 children in the CONTROL group received a single, age appropriate dose of a COVID-19 mRNA BNT162b2 vaccine during the study period. The frequency and character of reported adverse events (AEs) after each dose and results of flow cytometry (FC) 3 weeks after a second dose were compared between those groups. COVID-19 mRNA BNT162b2 vaccine safety profile was very good and comparable in both groups. No severe AEs were observed. 30% of all patients reported some general AE after any vaccine dose and 46% - some local AE. Frequency of reported AEs did not differ between groups except for local hardening at injection site, more common in PIMS group (20% vs 4% after any vaccine dose, p = 0,02). All AEs were benign, general AEs lasted up to 5 days and localised - up to 6 days after a vaccine dose. COVID-19 mRNA BNT162b2 vaccine did not induce any PIMS-like symptoms in any patient. We did not observe any significant T cells or B cells subset abnormalities in the PIMS group compared to the CONTROL group three weeks after a second dose except for terminally differentiated effector memory T cells that were higher in PIMS group (p < 0.0041). To sum up COVID-19 mRNA BNT162b2 vaccine in children with PIMS-TS was safe. Further studies are required to support our findings.

Dyscyplina PBN
nauki biologiczne
Czasopismo
Vaccine
Tom
41
Zeszyt
13
Strony od-do
2289-2299
ISSN
0264-410X
Data udostępnienia w otwartym dostępie
2023-03-02
Licencja otwartego dostępu
Uznanie autorstwa- Użycie niekomercyjne