Scientific Reports (Apr 2022)

SARS-CoV-2 Spike S1-specific IgG kinetic profiles following mRNA or vector-based vaccination in the general Dutch population show distinct kinetics

  • Lotus L. van den Hoogen,
  • Marije K. Verheul,
  • Eric R. A. Vos,
  • Cheyenne C. E. van Hagen,
  • Michiel van Boven,
  • Denise Wong,
  • Alienke J. Wijmenga-Monsuur,
  • Gaby Smits,
  • Marjan Kuijer,
  • Debbie van Rooijen,
  • Marjan Bogaard-van Maurik,
  • Ilse Zutt,
  • Jeffrey van Vliet,
  • Janine Wolf,
  • Fiona R. M. van der Klis,
  • Hester E. de Melker,
  • Robert S. van Binnendijk,
  • Gerco den Hartog

DOI
https://doi.org/10.1038/s41598-022-10020-6
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 6

Abstract

Read online

Abstract mRNA- and vector-based vaccines are used at a large scale to prevent COVID-19. We compared Spike S1-specific (S1) IgG antibodies after vaccination with mRNA-based (Comirnaty, Spikevax) or vector-based (Janssen, Vaxzevria) vaccines, using samples from a Dutch nationwide cohort. In adults 18–64 years old (n = 2412), the median vaccination interval between the two doses was 77 days for Vaxzevria (interquartile range, IQR: 69–77), 35 days (28–35) for Comirnaty and 33 days (28–35) for Spikevax. mRNA vaccines induced faster inclines and higher S1 antibodies compared to vector-based vaccines. For all vaccines, one dose resulted in boosting of S1 antibodies in adults with a history of SARS-CoV-2 infection. For Comirnaty, two to four months following the second dose (n = 196), S1 antibodies in adults aged 18–64 years old (436 BAU/mL, IQR: 328–891) were less variable and median concentrations higher compared to those in persons ≥ 80 years old (366, 177–743), but differences were not statistically significant (p > 0.100). Nearly all participants seroconverted following COVID-19 vaccination, including the aging population. These data confirm results from controlled vaccine trials in a general population, including vulnerable groups.