Multiple BCG vaccinations for the prevention of COVID-19 and other infectious diseases in type 1 diabetes

Cell Rep Med. 2022 Sep 20;3(9):100728. doi: 10.1016/j.xcrm.2022.100728. Epub 2022 Aug 15.

Abstract

There is a need for safe and effective platform vaccines to protect against coronavirus disease 2019 (COVID-19) and other infectious diseases. In this randomized, double-blinded, placebo-controlled phase 2/3 trial, we evaluate the safety and efficacy of a multi-dose Bacillus Calmette-Guérin (BCG) vaccine for the prevention of COVID-19 and other infectious disease in a COVID-19-unvaccinated, at-risk-community-based cohort. The at-risk population is made of up of adults with type 1 diabetes. We enrolled 144 subjects and randomized 96 to BCG and 48 to placebo. There were no dropouts over the 15-month trial. A cumulative incidence of 12.5% of placebo-treated and 1% of BCG-treated participants meets criteria for confirmed COVID-19, yielding an efficacy of 92%. The BCG group also displayed fewer infectious disease symptoms and lesser severity and fewer infectious disease events per patient, including COVID-19. There were no BCG-related systemic adverse events. BCG's broad-based infection protection suggests that it may provide platform protection against new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants and other pathogens.

Trial registration: ClinicalTrials.gov NCT02081326.

Keywords: BCG; Bacillus Calmette-Guérin; COVID-19; Clinicaltrials.gov: NCT02081326; autoimmune; host microbe interactions; hygiene hypothesis; infectious diseases; phase 2/3 trial; randomized double blinded clinical trial; type 1 diabetes; vaccine.

Publication types

  • Clinical Trial, Phase II
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • BCG Vaccine / therapeutic use
  • COVID-19* / prevention & control
  • Communicable Diseases*
  • Diabetes Mellitus, Type 1* / drug therapy
  • Humans
  • Mycobacterium bovis*
  • SARS-CoV-2
  • Vaccination

Substances

  • BCG Vaccine

Associated data

  • ClinicalTrials.gov/NCT02081326