BMJ Open (Feb 2023)

Cohort profile: A Québec-based plasma donor biobank to study COVID-19 immunity (PlasCoV)

  • Antoine Lewin,
  • Mélanie Dieudé,
  • Marc Germain,
  • Renée Bazin,
  • Josée Perreault,
  • Amélie Boivin,
  • Yves Grégoire,
  • Christian Renaud

DOI
https://doi.org/10.1136/bmjopen-2022-068803
Journal volume & issue
Vol. 13, no. 2

Abstract

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Purpose The long-term humoral immunity to COVID-19 is not well understood owing to the continuous emergence of new variants of concern, the evolving vaccine-induced and infection-induced immunity, and the limited duration of follow-up in previous studies. As the sole blood service in Québec (Canada), Héma-Québec established a COVID-19-focused biobank (‘PlasCoV’) in April 2021.Participants As of January 2022, the biobank included 86 483 plasma samples from 15 502 regular donors (age range=18–84 years, females=49.7%), for an average of 5.6 donations per donor. Nearly two-thirds (65.6%) of biobank donors made at least two donations, with many donors having provided samples prevaccination and postvaccination (3061 (19.7%)) or preinfection and postinfection (131 (0.8%)), thus allowing for longitudinal studies on vaccine-induced and infection-induced immunity.Findings to date A study that used PlasCoV samples revealed that previously infected individuals who received a single dose of the BNT162b2 COVID-19 vaccine exhibited the strongest immune response. By contrast, SARS-CoV-2-naïve individuals required two vaccine doses to produce a maximal immune response. Furthermore, the results of a four-phase seroprevalence study indicated that the antinucleocapsid (N) response wanes rapidly, so that up to one-third of previously infected donors were seronegative for anti-N.Future plans Donations from individuals who consented to participate before 1 October 2022 will be collected up until 31 March 2023. This plasma biobank will facilitate the conduct of longitudinal studies on COVID-19 immunity, thus helping to provide valuable insights into the anti-SARS-CoV-2 immune response and its persistence, and the effects of vaccination and variants on the specificity of the anti-SARS-CoV-2 immune response.