Immune Response to Vaccination against COVID-19 at Different Second-Dose Intervals and Their Associations with Metabolic Parameters.
Łukasz SzczerbińskiMichał Andrzej OkruszkoMaciej SzabłowskiJędrzej WarpechowskiAdam PaszkoAnna CitkoPaulina KonopkaWitold BauerAdam Jacek KrętowskiPublished in: Vaccines (2023)
Obesity and diabetes are associated with severe outcomes of coronavirus disease (COVID-19). Vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been proven protective against infection and severe COVID-19. However, the immune response of metabolically burdened individuals to the vaccines remains unclear. Thus, we aimed to assess whether the metabolic status of individuals affects their humoral immune responses to the vaccination. Moreover, we evaluated whether the interval between the first two doses influenced antibody concentration. Sixty-seven individuals (21 males, 46 females) were vaccinated with the BNT162b2 mRNA COVID-19 vaccine. Fifty-four individuals were vaccinated with the second dose after 3 weeks and 13 after 5 weeks. We measured the antibody titers in all participants during the 19-week follow-up period. Patients diagnosed with COVID-19 were excluded. In the 5-week interval group, a significantly higher level of maximal antibody titers was observed. However, there were no differences in antibody concentrations after 19 weeks and no significant correlation between cardiometabolic factors and humoral response. The elongation of second-dose timing to 5 weeks leads to a higher acute antibody response but does not change long-term levels of antibody titers. Moreover, dysregulation of metabolic parameters does not lead to a diminished immune response to vaccination.
Keyphrases
- coronavirus disease
- sars cov
- immune response
- respiratory syndrome coronavirus
- type diabetes
- dendritic cells
- end stage renal disease
- toll like receptor
- chronic kidney disease
- early onset
- cardiovascular disease
- metabolic syndrome
- randomized controlled trial
- ejection fraction
- clinical trial
- weight loss
- heart rate
- liver failure
- patient reported outcomes
- drug induced
- inflammatory response
- skeletal muscle
- blood pressure
- hepatitis b virus
- peritoneal dialysis
- respiratory failure
- binding protein
- extracorporeal membrane oxygenation