TY - JOUR
T1 - BCG Vaccination of Health Care Workers Does Not Reduce SARS-CoV-2 Infections nor Infection Severity or Duration
T2 - a Randomized Placebo-Controlled Trial
AU - Claus, Juana
AU - Ten Doesschate, Thijs
AU - Gumbs, Cheyenne
AU - van Werkhoven, Cornelis H
AU - van der Vaart, Thomas W
AU - Janssen, Axel B
AU - Smits, Gaby
AU - van Binnendijk, Rob
AU - van der Klis, Fiona
AU - van Baarle, Debbie
AU - Paganelli, Fernanda L
AU - Leavis, Helen
AU - Verhagen, Lilly M
AU - Joosten, Simone A
AU - Bonten, Marc J M
AU - Netea, Mihai G
AU - van de Wijgert, Janneke H H M
N1 - Funding Information:
We thank the health care workers for their participation, Katina Kardaminidis for trial management, Frank Leus and Roxanne Schaakx for data management, and all other colleagues in the participating hospitals who implemented the BCG-Corona trial, and the sample collection and testing, under difficult circumstances. The original BCG-Corona trial was not externally funded. The additional work included in this publication is part of the project “BCG vaccination to minimize COVID-19 disease severity and duration” with project number 10430 01 201 0026 of the research program COVID-19 which is financed by the Netherlands Organization for Health Research and Development (ZonMw). M.G.N. was also funded by an ERC Advanced Grant (833247) and Spinoza grant of the Netherlands Organization for Scientific Research (NWO). L.M.V. was also funded by a Wilhelmina Children’s Hospital (Utrecht) grant and a Hypatia Tenure Track grant of the Radboud University Medical Center (Nijmegen). The funders did not have any role in the collection, analysis, and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication.V.
Publisher Copyright:
© 2023 American Society for Microbiology. All rights reserved.
PY - 2023/4/25
Y1 - 2023/4/25
N2 - Bacillus Calmette-Guerin (BCG) vaccination has been hypothesized to reduce severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, severity, and/or duration via trained immunity induction. Health care workers (HCWs) in nine Dutch hospitals were randomized to BCG or placebo vaccination (1:1) in March and April 2020 and followed for 1 year. They reported daily symptoms, SARS-CoV-2 test results, and health care-seeking behavior via a smartphone application, and they donated blood for SARS-CoV-2 serology at two time points. A total of 1,511 HCWs were randomized and 1,309 analyzed (665 BCG and 644 placebo). Of the 298 infections detected during the trial, 74 were detected by serology only. The SARS-CoV-2 incidence rates were 0.25 and 0.26 per person-year in the BCG and placebo groups, respectively (incidence rate ratio, 0.95; 95% confidence interval, 0.76 to 1.21;
P = 0.732). Only three participants required hospitalization for SARS-CoV-2. The proportions of participants with asymptomatic, mild, or moderate infections and the mean infection durations did not differ between randomization groups. In addition, unadjusted and adjusted logistic regression and Cox proportional hazards models showed no differences between BCG and placebo vaccination for any of these outcomes. The percentage of participants with seroconversion (7.8% versus 2.8%;
P = 0.006) and mean SARS-CoV-2 anti-S1 antibody concentration (13.1 versus 4.3 IU/mL;
P = 0.023) were higher in the BCG than placebo group at 3 months but not at 6 or 12 months postvaccination. BCG vaccination of HCWs did not reduce SARS-CoV-2 infections nor infection duration or severity (ranging from asymptomatic to moderate). In the first 3 months after vaccination, BCG vaccination may enhance SARS-CoV-2 antibody production during SARS-CoV-2 infection.
IMPORTANCE While several BCG trials in adults were conducted during the 2019 coronavirus disease epidemic, our data set is the most comprehensive to date, because we included serologically confirmed infections in addition to self-reported positive SARS-CoV-2 test results. We also collected data on symptoms for every day during the 1-year follow-up period, which enabled us to characterize infections in detail. We found that BCG vaccination did not reduce SARS-CoV-2 infections nor infection duration or severity but may have enhanced SARS-CoV-2 antibody production during SARS-CoV-2 infection in the first 3 months after vaccination. These results are in agreement with other BCG trials that reported negative results (but did not use serological endpoints), except for two trials in Greece and India that reported positive results but had few endpoints and included endpoints that were not laboratory confirmed. The enhanced antibody production is in agreement with prior mechanistic studies but did not translate into protection from SARS-CoV-2 infection.
AB - Bacillus Calmette-Guerin (BCG) vaccination has been hypothesized to reduce severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, severity, and/or duration via trained immunity induction. Health care workers (HCWs) in nine Dutch hospitals were randomized to BCG or placebo vaccination (1:1) in March and April 2020 and followed for 1 year. They reported daily symptoms, SARS-CoV-2 test results, and health care-seeking behavior via a smartphone application, and they donated blood for SARS-CoV-2 serology at two time points. A total of 1,511 HCWs were randomized and 1,309 analyzed (665 BCG and 644 placebo). Of the 298 infections detected during the trial, 74 were detected by serology only. The SARS-CoV-2 incidence rates were 0.25 and 0.26 per person-year in the BCG and placebo groups, respectively (incidence rate ratio, 0.95; 95% confidence interval, 0.76 to 1.21;
P = 0.732). Only three participants required hospitalization for SARS-CoV-2. The proportions of participants with asymptomatic, mild, or moderate infections and the mean infection durations did not differ between randomization groups. In addition, unadjusted and adjusted logistic regression and Cox proportional hazards models showed no differences between BCG and placebo vaccination for any of these outcomes. The percentage of participants with seroconversion (7.8% versus 2.8%;
P = 0.006) and mean SARS-CoV-2 anti-S1 antibody concentration (13.1 versus 4.3 IU/mL;
P = 0.023) were higher in the BCG than placebo group at 3 months but not at 6 or 12 months postvaccination. BCG vaccination of HCWs did not reduce SARS-CoV-2 infections nor infection duration or severity (ranging from asymptomatic to moderate). In the first 3 months after vaccination, BCG vaccination may enhance SARS-CoV-2 antibody production during SARS-CoV-2 infection.
IMPORTANCE While several BCG trials in adults were conducted during the 2019 coronavirus disease epidemic, our data set is the most comprehensive to date, because we included serologically confirmed infections in addition to self-reported positive SARS-CoV-2 test results. We also collected data on symptoms for every day during the 1-year follow-up period, which enabled us to characterize infections in detail. We found that BCG vaccination did not reduce SARS-CoV-2 infections nor infection duration or severity but may have enhanced SARS-CoV-2 antibody production during SARS-CoV-2 infection in the first 3 months after vaccination. These results are in agreement with other BCG trials that reported negative results (but did not use serological endpoints), except for two trials in Greece and India that reported positive results but had few endpoints and included endpoints that were not laboratory confirmed. The enhanced antibody production is in agreement with prior mechanistic studies but did not translate into protection from SARS-CoV-2 infection.
KW - Bacillus Calmette-Guerin vaccine
KW - COVID-19
KW - SARS-CoV-2
KW - health care workers
KW - randomized placebo-controlled clinical trial
UR - http://www.scopus.com/inward/record.url?scp=85153899803&partnerID=8YFLogxK
U2 - 10.1128/mbio.00356-23
DO - 10.1128/mbio.00356-23
M3 - Article
C2 - 36976004
SN - 2150-7511
VL - 14
JO - mBio
JF - mBio
IS - 2
M1 - e0035623
ER -