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Randomized Trial of BCG Vaccine to Protect against Covid-19 in Health Care Workers. BACKGROUND: The bacille Calmette-Guérin (BCG) vaccine has immunomodulatory "off-target" effects that have been hypothesized to protect against coronavirus disease 2019 (Covid-19). METHODS: In this international, double-blind, placebo-controlled trial, we randomly assigned health care workers to receive the BCG-Denmark vaccine or saline placebo and followed them for 12 months. Symptomatic Covid-19 and severe Covid-19, the primary outcomes, were assessed at 6 months; the primary analyses involved the modified intention-to-treat population, which was restricted to participants with a negative test for severe acute respiratory syndrome coronavirus 2 at baseline. RESULTS: A total of 3988 participants underwent randomization; recruitment ceased before the planned sample size was reached owing to the availability of Covid-19 vaccines. The modified intention-to-treat population included 84.9% of the participants who underwent randomization: 1703 in the BCG group and 1683 in the placebo group. The estimated risk of symptomatic Covid-19 by 6 months was 14.7% in the BCG group and 12.3% in the placebo group (risk difference, 2.4 percentage points; 95% confidence interval [CI], -0.7 to 5.5; P = 0.13). The risk of severe Covid-19 by 6 months was 7.6% in the BCG group and 6.5% in the placebo group (risk difference, 1.1 percentage points; 95% CI, -1.2 to 3.5; P = 0.34); the majority of participants who met the trial definition of severe Covid-19 were not hospitalized but were unable to work for at least 3 consecutive days. In supplementary and sensitivity analyses that used less conservative censoring rules, the risk differences were similar but the confidence intervals were narrower. There were five hospitalizations due to Covid-19 in each group (including one death in the placebo group). The hazard ratio for any Covid-19 episode in the BCG group as compared with the placebo group was 1.23 (95% CI, 0.96 to 1.59). No safety concerns were identified. CONCLUSIONS: Vaccination with BCG-Denmark did not result in a lower risk of Covid-19 among health care workers than placebo. (Funded by the Bill and Melinda Gates Foundation and others; BRACE ClinicalTrials.gov number, NCT04327206.).

This phase 3, multicenter, randomized, controlled trial involving health care workers was conducted in two stages. Stage 1 (recruitment from March 2020 through May 2020) took place in Australia only. Stage 2 (recruitment from May 2020 through April 2021) took place in Australia, the Netherlands, Spain, the United Kingdom, and Brazil. In the double-blind stage 2 part of the trial, participants were randomly assigned in a 1:1 ratio to receive intradermal BCG-Denmark vaccine or saline placebo and were followed for 12 months, with the primary outcomes assessed at 6 months.10 As prespecified in our statistical analysis plan,11 this report focuses only on stage 2 of the trial because there was negligible SARS-CoV-2 community transmission during stage 1. The protocol, which has been published previously,10 and the statistical analysis plan are available with the full text of this article at NEJM.org. The trial was approved by the ethics committee at each site and overseen by a steering committee and an independent data and safety monitoring board. The investigators designed the trial. A subgroup of authors collected and analyzed the data. The first four authors and last two authors vouch for the accuracy and completeness of the data and for the fidelity of the trial to the protocol. The funders had no role in the collection, analysis, or interpretation of data or in the preparation, review, or approval of the manuscript.

collected and analyzed the data. The first four authors and last two authors vouch for the accuracy and completeness of the data and for the fidelity of the trial to the protocol. The funders had no role in the collection, analysis, or interpretation of data or in the preparation, review, or approval of the manuscript. The eligibility of potential participants was ascertained during a baseline visit. Exclusion criteria included a previous positive SARS-CoV-2 test; contraindication to the BCG vaccine; receipt of BCG vaccine within the past year, any other live-attenuated vaccine within the past month, or any Covid-19–specific vaccine; and involvement in another Covid-19 prevention trial. At baseline, blood samples were obtained from all the participants for SARS-CoV-2 serologic testing; in Brazil, respiratory swab samples were also obtained for SARS-CoV-2 polymerase-chain-reaction (PCR) assay. All the participants provided written informed consent. The computer-generated randomization list was prepared by an independent statistician, and we used Web-based randomization, accessed by trial staff after consent had been obtained and baseline assessments had been performed. Randomization was stratified according to geographic region (Brazil, Europe, or Australia), age group (<40 years, 40 to 59 years, or ≥60 years), and the presence or absence of a coexisting condition. Participants, investigators, outcome assessors, data managers, trial statisticians, and trial staff were unaware of the trial-group assignments throughout the trial.

graphic region (Brazil, Europe, or Australia), age group (<40 years, 40 to 59 years, or ≥60 years), and the presence or absence of a coexisting condition. Participants, investigators, outcome assessors, data managers, trial statisticians, and trial staff were unaware of the trial-group assignments throughout the trial. A single dose of 0.1 ml of BCG-Denmark vaccine (AJ Vaccines; corresponding to 2 to 8×105 colony-forming units [CFUs] of Mycobacterium bovis, Danish strain 1331) or saline placebo was administered as an intradermal injection in the region of the deltoid muscle. A photograph was taken of the injection-site “bleb” (a small blister on the skin) to confirm correct administration.

es; corresponding to 2 to 8×105 colony-forming units [CFUs] of Mycobacterium bovis, Danish strain 1331) or saline placebo was administered as an intradermal injection in the region of the deltoid muscle. A photograph was taken of the injection-site “bleb” (a small blister on the skin) to confirm correct administration. The trial had two primary outcomes: the incidence of symptomatic Covid-19 and the incidence of severe Covid-19 by 6 months after randomization. Complete definitions of the primary and secondary outcomes are provided in the Supplementary Appendix, available at NEJM.org. In brief, symptomatic Covid-19 was defined, in accordance with the case definition used internationally at the start of the trial, as an episode of illness with fever or at least one symptom of respiratory disease (including sore throat, cough, and shortness of breath) and evidence of SARS-CoV-2 infection on PCR assay, rapid antigen test, or serologic test. Severe Covid-19 was defined as an episode of illness with evidence of SARS-CoV-2 infection (on PCR assay, rapid antigen test, or serologic test) plus at least one of the following as a consequence of Covid-19: death, hospitalization, or severe disease without hospitalization (defined, for the purpose of this trial, as being confined to bed or unable to work for ≥3 consecutive days, not resulting from quarantine or other restrictions).

n test, or serologic test) plus at least one of the following as a consequence of Covid-19: death, hospitalization, or severe disease without hospitalization (defined, for the purpose of this trial, as being confined to bed or unable to work for ≥3 consecutive days, not resulting from quarantine or other restrictions). Secondary outcomes included the time to onset of Covid-19; the number of Covid-19 episodes; the number of days with symptoms, absent from work, or confined to bed; complications (including pneumonia, receipt of oxygen, hospitalization, admission to a critical care unit, use of mechanical ventilation, or death); and asymptomatic infection. All these outcomes were assessed until 6 months after randomization. Vaccine-related adverse reactions were also monitored. The REDCap platform was used for data collection.12 Participants were asked weekly if they had been unwell with the use of a custom-built smartphone application (Trial Symptom Tracker, WeGuide), direct contact (telephone call or text message), or both. During each episode of illness, symptoms were recorded daily, and participants were asked to undergo SARS-CoV-2 testing. More detailed questionnaires were completed at baseline and every 3 months during follow-up. Additional information on hospitalizations was obtained from medical records. Blood samples were obtained at baseline and 3, 6, 9, and 12 months after randomization for measurement of anti–SARS-CoV-2 nucleocapsid antibodies (Roche Cobas Elecsys anti–SARS-CoV-2 assay).13 A biobank of other samples was also established.

Additional information on hospitalizations was obtained from medical records. Blood samples were obtained at baseline and 3, 6, 9, and 12 months after randomization for measurement of anti–SARS-CoV-2 nucleocapsid antibodies (Roche Cobas Elecsys anti–SARS-CoV-2 assay).13 A biobank of other samples was also established. The statistical analysis plan14 was finalized and made publicly available before unblinding; full details, including the sample-size calculation (planned sample, 7244 participants), are available in the Supplementary Appendix. For the primary outcomes, survival analysis (with adjustment for stratification factors) was used to estimate the proportion of participants with a Covid-19 episode by 6 months in each group and the risk difference. Follow-up data were censored at 6 months, or at the time of receipt of the first Covid-19–specific vaccine, or when it could not be ascertained whether a Covid-19 episode had occurred (missing data for ≥3 consecutive days or an illness episode without a Covid-19 test result). Most analyses were performed in the modified intention-to-treat population, which was restricted to participants with a negative baseline SARS-CoV-2 test.

when it could not be ascertained whether a Covid-19 episode had occurred (missing data for ≥3 consecutive days or an illness episode without a Covid-19 test result). Most analyses were performed in the modified intention-to-treat population, which was restricted to participants with a negative baseline SARS-CoV-2 test. Prespecified supplementary analyses were performed to provide additional insights; separate analyses included follow-up time after receipt of a Covid-19–specific vaccine, excluded episodes that started within 14 days after randomization, censored data from participants at any subsequent vaccination (e.g., influenza vaccine), and involved the intention-to-treat population. Sensitivity analyses were also performed; separate analyses were restricted to episodes occurring on or after the date of receipt of BCG vaccine or placebo, used results from PCR assays and rapid antigen tests only (without serologic results) to define Covid-19 episodes (in the intention-to-treat population), and used less conservative censoring rules for missing data. Table S1 in the Supplementary Appendix details the primary, sensitivity, and supplementary estimands. Prespecified subgroup analyses were performed on the basis of age group (<40 years, 40 to 59 years, or ≥60 years), the presence of a coexisting condition (yes or no, and according to condition), geographic region (Brazil, Europe, or Australia), sex (male or female), and previous BCG vaccination (yes or no) for the primary analysis.

This phase 3, multicenter, randomized, controlled trial involving health care workers was conducted in two stages. Stage 1 (recruitment from March 2020 through May 2020) took place in Australia only. Stage 2 (recruitment from May 2020 through April 2021) took place in Australia, the Netherlands, Spain, the United Kingdom, and Brazil. In the double-blind stage 2 part of the trial, participants were randomly assigned in a 1:1 ratio to receive intradermal BCG-Denmark vaccine or saline placebo and were followed for 12 months, with the primary outcomes assessed at 6 months.10 As prespecified in our statistical analysis plan,11 this report focuses only on stage 2 of the trial because there was negligible SARS-CoV-2 community transmission during stage 1. The protocol, which has been published previously,10 and the statistical analysis plan are available with the full text of this article at NEJM.org.

The trial was approved by the ethics committee at each site and overseen by a steering committee and an independent data and safety monitoring board. The investigators designed the trial. A subgroup of authors collected and analyzed the data. The first four authors and last two authors vouch for the accuracy and completeness of the data and for the fidelity of the trial to the protocol. The funders had no role in the collection, analysis, or interpretation of data or in the preparation, review, or approval of the manuscript.

The eligibility of potential participants was ascertained during a baseline visit. Exclusion criteria included a previous positive SARS-CoV-2 test; contraindication to the BCG vaccine; receipt of BCG vaccine within the past year, any other live-attenuated vaccine within the past month, or any Covid-19–specific vaccine; and involvement in another Covid-19 prevention trial. At baseline, blood samples were obtained from all the participants for SARS-CoV-2 serologic testing; in Brazil, respiratory swab samples were also obtained for SARS-CoV-2 polymerase-chain-reaction (PCR) assay. All the participants provided written informed consent.

The computer-generated randomization list was prepared by an independent statistician, and we used Web-based randomization, accessed by trial staff after consent had been obtained and baseline assessments had been performed. Randomization was stratified according to geographic region (Brazil, Europe, or Australia), age group (<40 years, 40 to 59 years, or ≥60 years), and the presence or absence of a coexisting condition. Participants, investigators, outcome assessors, data managers, trial statisticians, and trial staff were unaware of the trial-group assignments throughout the trial.

A single dose of 0.1 ml of BCG-Denmark vaccine (AJ Vaccines; corresponding to 2 to 8×105 colony-forming units [CFUs] of Mycobacterium bovis, Danish strain 1331) or saline placebo was administered as an intradermal injection in the region of the deltoid muscle. A photograph was taken of the injection-site “bleb” (a small blister on the skin) to confirm correct administration.

The trial had two primary outcomes: the incidence of symptomatic Covid-19 and the incidence of severe Covid-19 by 6 months after randomization. Complete definitions of the primary and secondary outcomes are provided in the Supplementary Appendix, available at NEJM.org. In brief, symptomatic Covid-19 was defined, in accordance with the case definition used internationally at the start of the trial, as an episode of illness with fever or at least one symptom of respiratory disease (including sore throat, cough, and shortness of breath) and evidence of SARS-CoV-2 infection on PCR assay, rapid antigen test, or serologic test. Severe Covid-19 was defined as an episode of illness with evidence of SARS-CoV-2 infection (on PCR assay, rapid antigen test, or serologic test) plus at least one of the following as a consequence of Covid-19: death, hospitalization, or severe disease without hospitalization (defined, for the purpose of this trial, as being confined to bed or unable to work for ≥3 consecutive days, not resulting from quarantine or other restrictions). Secondary outcomes included the time to onset of Covid-19; the number of Covid-19 episodes; the number of days with symptoms, absent from work, or confined to bed; complications (including pneumonia, receipt of oxygen, hospitalization, admission to a critical care unit, use of mechanical ventilation, or death); and asymptomatic infection. All these outcomes were assessed until 6 months after randomization. Vaccine-related adverse reactions were also monitored.

The REDCap platform was used for data collection.12 Participants were asked weekly if they had been unwell with the use of a custom-built smartphone application (Trial Symptom Tracker, WeGuide), direct contact (telephone call or text message), or both. During each episode of illness, symptoms were recorded daily, and participants were asked to undergo SARS-CoV-2 testing. More detailed questionnaires were completed at baseline and every 3 months during follow-up. Additional information on hospitalizations was obtained from medical records. Blood samples were obtained at baseline and 3, 6, 9, and 12 months after randomization for measurement of anti–SARS-CoV-2 nucleocapsid antibodies (Roche Cobas Elecsys anti–SARS-CoV-2 assay).13 A biobank of other samples was also established.

The statistical analysis plan14 was finalized and made publicly available before unblinding; full details, including the sample-size calculation (planned sample, 7244 participants), are available in the Supplementary Appendix. For the primary outcomes, survival analysis (with adjustment for stratification factors) was used to estimate the proportion of participants with a Covid-19 episode by 6 months in each group and the risk difference. Follow-up data were censored at 6 months, or at the time of receipt of the first Covid-19–specific vaccine, or when it could not be ascertained whether a Covid-19 episode had occurred (missing data for ≥3 consecutive days or an illness episode without a Covid-19 test result). Most analyses were performed in the modified intention-to-treat population, which was restricted to participants with a negative baseline SARS-CoV-2 test.

From May 14, 2020, through April 1, 2021, a total of 3988 participants were randomly assigned to receive BCG vaccine (1999 participants) or placebo (1989 participants) (Figure 1). Recruitment was stopped prematurely before the planned sample size was reached because of the global rollout of Covid-19–specific vaccines. The baseline characteristics were similar in the two groups (Table 1 and Tables S2 and S3), apart from a slightly higher percentage of female participants in the placebo group than in the BCG group (75.1% vs. 72.3%). Participants were predominantly women (73.7%), with a mean (±SD) age of 42.0±12.1 years. A large proportion of the participants were enrolled in Brazil (64.4%). Information on the representativeness of the trial participants is provided in Table S20. The baseline SARS-CoV-2 serologic status was positive in 14.1% of all the participants, and the baseline SARS-CoV-2 swab was positive in 2.7% of Brazilian participants (and inconclusive or missing in 0.5%). The modified intention-to-treat population consequently included 84.9% of the participants who underwent randomization (Figure 1): 1703 in the BCG group and 1683 in the placebo group (Table 1). Overall, 98.0% of the participants were followed for 6 months or more, with a similar percentage in the two groups (Table S5).

The modified intention-to-treat population consequently included 84.9% of the participants who underwent randomization (Figure 1): 1703 in the BCG group and 1683 in the placebo group (Table 1). Overall, 98.0% of the participants were followed for 6 months or more, with a similar percentage in the two groups (Table S5). In the first 6 months after randomization (modified intention-to-treat population), symptomatic Covid-19 occurred in 132 participants in the BCG group (adjusted estimated risk, 14.7%) and in 106 participants in the placebo group (12.3%) (difference, 2.4 percentage points; 95% confidence interval [CI], −0.7 to 5.5; P=0.13); severe Covid-19, as defined in this trial, occurred in 75 participants in the BCG group (7.6%) and in 61 participants in the placebo group (6.5%) (difference, 1.1 percentage points; 95% CI, −1.2 to 3.5; P=0.34) (Table 2, Figure 2, and Tables S7 and S8). The majority of participants who met the trial definition of severe Covid-19 were not hospitalized but were unable to work for at least 3 consecutive days. In supplementary and sensitivity analyses that used less conservative censoring rules, the risk differences were similar but the confidence intervals were narrower (Figure 2). This included the sensitivity analyses using results from PCR assays and rapid antigen tests only (without serologic results) and the analyses that did not account for Covid-19–specific vaccination.

ss conservative censoring rules, the risk differences were similar but the confidence intervals were narrower (Figure 2). This included the sensitivity analyses using results from PCR assays and rapid antigen tests only (without serologic results) and the analyses that did not account for Covid-19–specific vaccination. Results for the secondary outcomes are presented in Table 2 and Table S9 through S17. The probability of any Covid-19 episode within 6 months was greater in the BCG group than in the placebo group, although the confidence interval was wide and included no difference between the two groups (adjusted hazard ratio, 1.23; 95% CI, 0.96 to 1.59) (Table 2). In sensitivity analyses that were based on the results of PCR assays and rapid antigen tests only (adjusted hazard ratio, 1.38; 95% CI, 1.05 to 1.81) and the analyses that did not account for Covid-19–specific vaccination (adjusted hazard ratio, 1.24; 95% CI, 1.01 to 1.53), extended follow-up time resulted in more precise estimates and confidence intervals that excluded no difference between the two groups (Fig. S3). Five hospitalizations due to Covid-19 occurred in each group (including one death in the placebo group).

ific vaccination (adjusted hazard ratio, 1.24; 95% CI, 1.01 to 1.53), extended follow-up time resulted in more precise estimates and confidence intervals that excluded no difference between the two groups (Fig. S3). Five hospitalizations due to Covid-19 occurred in each group (including one death in the placebo group). When the number of days with symptoms was compared between the BCG group and the placebo group, there was strong evidence of an interaction between the trial group and two randomization strata (age group and the presence or absence of a coexisting condition), which rendered an overall comparison between randomization groups noninterpretable. Post hoc subgroup analyses showed that among participants 60 years of age or older, the BCG group had fewer days with symptoms than the placebo group (incidence rate ratio, 0.32; 95% CI, 0.19 to 0.53) (Table 2 and Fig. S4), whereas no substantial difference between trial groups was seen among participants younger than 40 years of age and those 40 to 59 years of age. In the subgroup without coexisting conditions, the BCG group had fewer days with symptoms than the placebo group (incidence rate ratio, 0.73; 95% CI, 0.58 to 0.91), but the opposite was true in those with coexisting conditions (incidence rate ratio, 1.49; 95% CI, 0.88 to 2.52).

s of age and those 40 to 59 years of age. In the subgroup without coexisting conditions, the BCG group had fewer days with symptoms than the placebo group (incidence rate ratio, 0.73; 95% CI, 0.58 to 0.91), but the opposite was true in those with coexisting conditions (incidence rate ratio, 1.49; 95% CI, 0.88 to 2.52). In prespecified subgroup analyses, there was little evidence that the treatment effect differed across most of the subgroups (Figure 3). With respect to the influence of previous BCG vaccination, the results are consistent with the possibility of a greater risk of severe Covid-19 in the BCG group than in the placebo group among participants who had not previously received BCG vaccination but not among those who received BCG revaccination. The probability of symptomatic or severe Covid-19 by 6 months appeared to be slightly higher in the BCG group than in the placebo group among participants with cardiovascular disease, those with hypertension, and those with chronic respiratory disease. In the sex subgroup analysis, although there was minimal evidence of an interaction between sex and the effect of BCG vaccination, the disease-free survival curves separated earlier in the male subgroup than in the female subgroup (Figs. S1 and S2).

, those with hypertension, and those with chronic respiratory disease. In the sex subgroup analysis, although there was minimal evidence of an interaction between sex and the effect of BCG vaccination, the disease-free survival curves separated earlier in the male subgroup than in the female subgroup (Figs. S1 and S2). Details on adverse events are provided in Tables S18 and S19. A total of 29 participants reported 30 serious adverse events: 20 in the BCG group and 9 in the placebo group. Apart from a painful injection-site abscess with lethargy in the BCG group, all serious adverse events were considered by the site investigator to be unrelated to the intervention.

In the first 6 months after randomization (modified intention-to-treat population), symptomatic Covid-19 occurred in 132 participants in the BCG group (adjusted estimated risk, 14.7%) and in 106 participants in the placebo group (12.3%) (difference, 2.4 percentage points; 95% confidence interval [CI], −0.7 to 5.5; P=0.13); severe Covid-19, as defined in this trial, occurred in 75 participants in the BCG group (7.6%) and in 61 participants in the placebo group (6.5%) (difference, 1.1 percentage points; 95% CI, −1.2 to 3.5; P=0.34) (Table 2, Figure 2, and Tables S7 and S8). The majority of participants who met the trial definition of severe Covid-19 were not hospitalized but were unable to work for at least 3 consecutive days. In supplementary and sensitivity analyses that used less conservative censoring rules, the risk differences were similar but the confidence intervals were narrower (Figure 2). This included the sensitivity analyses using results from PCR assays and rapid antigen tests only (without serologic results) and the analyses that did not account for Covid-19–specific vaccination.

Results for the secondary outcomes are presented in Table 2 and Table S9 through S17. The probability of any Covid-19 episode within 6 months was greater in the BCG group than in the placebo group, although the confidence interval was wide and included no difference between the two groups (adjusted hazard ratio, 1.23; 95% CI, 0.96 to 1.59) (Table 2). In sensitivity analyses that were based on the results of PCR assays and rapid antigen tests only (adjusted hazard ratio, 1.38; 95% CI, 1.05 to 1.81) and the analyses that did not account for Covid-19–specific vaccination (adjusted hazard ratio, 1.24; 95% CI, 1.01 to 1.53), extended follow-up time resulted in more precise estimates and confidence intervals that excluded no difference between the two groups (Fig. S3). Five hospitalizations due to Covid-19 occurred in each group (including one death in the placebo group).

In prespecified subgroup analyses, there was little evidence that the treatment effect differed across most of the subgroups (Figure 3). With respect to the influence of previous BCG vaccination, the results are consistent with the possibility of a greater risk of severe Covid-19 in the BCG group than in the placebo group among participants who had not previously received BCG vaccination but not among those who received BCG revaccination. The probability of symptomatic or severe Covid-19 by 6 months appeared to be slightly higher in the BCG group than in the placebo group among participants with cardiovascular disease, those with hypertension, and those with chronic respiratory disease. In the sex subgroup analysis, although there was minimal evidence of an interaction between sex and the effect of BCG vaccination, the disease-free survival curves separated earlier in the male subgroup than in the female subgroup (Figs. S1 and S2).

Details on adverse events are provided in Tables S18 and S19. A total of 29 participants reported 30 serious adverse events: 20 in the BCG group and 9 in the placebo group. Apart from a painful injection-site abscess with lethargy in the BCG group, all serious adverse events were considered by the site investigator to be unrelated to the intervention.

In this multisite, double-blind, randomized, controlled trial involving health care workers in five countries, vaccination with BCG-Denmark did not result in a lower risk of Covid-19 within 6 months than placebo. It is notable that the risk of an episode of Covid-19 was higher in the BCG group than in the placebo group, although the confidence interval around this estimate was wide and crossed zero.

e workers in five countries, vaccination with BCG-Denmark did not result in a lower risk of Covid-19 within 6 months than placebo. It is notable that the risk of an episode of Covid-19 was higher in the BCG group than in the placebo group, although the confidence interval around this estimate was wide and crossed zero. Previous studies that investigated the ability of the BCG vaccine to protect against Covid-19 in adults15-23 and in animal models24-27 have shown conflicting results. Retrospective and ecologic studies investigating the association between Covid-19 and history of BCG vaccination or national BCG vaccination policy or coverage are intrinsically limited by many biases, including the long period between BCG vaccination and SARS-CoV-2 exposure.15 Trials have also shown conflicting results.16-23 In a nonrandomized trial involving 280 health care workers in the United Arab Emirates, of 71 participants who received BCG revaccination (BCG-Russia), none reported Covid-19, as compared with 18 of 209 participants (8.6%) who declined revaccination.22 In contrast, randomized, controlled trials of BCG vaccination, with the exception of one, have shown no protective effect against Covid-19. In ACTIVATE-2 (A Randomized Clinical Trial for Enhanced Trained Immune Responses through BCG Vaccination to Prevent Infections by COVID-19), which involved 301 participants 50 years of age or older in Greece, the cumulative incidence of “presumed Covid-19” was lower after the receipt of BCG-Moscow vaccine than after the receipt of placebo, but the primary outcome was defined as possible, probable, or definite Covid-19 (without the requirement for a positive SARS-CoV-2 test).16 When the incidence of PCR-proven Covid-19 cases was assessed, the difference between the two groups was not significant.16 The BCG-CORONA trial, which involved 1000 participants in South Africa, showed a higher risk of severe respiratory tract infections after BCG revaccination (BCG-Denmark) than after receipt of placebo but no effect on Covid-19 risk.

ovid-19 cases was assessed, the difference between the two groups was not significant.16 The BCG-CORONA trial, which involved 1000 participants in South Africa, showed a higher risk of severe respiratory tract infections after BCG revaccination (BCG-Denmark) than after receipt of placebo but no effect on Covid-19 risk. However, the risk of hospitalization due to Covid-19 was twice as high in the BCG group as in the placebo group, but the confidence interval was wide and included 1 (hazard ratio, 2.0; 95% CI, 0.7 to 5.9; P=0.20).17 In two trials conducted in the Netherlands, BCG-Denmark vaccination had no effect on the incidence of Covid-19 episodes (as a secondary outcome) among health care workers (1511 participants)18 or among participants 60 years of age or older (2014 participants).19 In a trial involving 138 participants in Brazil, BCG revaccination of health care workers with BCG-Moscow did not protect against Covid-19.20 Similar findings were reported in a trial involving 354 participants in Poland after BCG revaccination with BCG-Moreau.21 Finally, in an ongoing trial investigating the effect of BCG vaccination on glycemic control in patients with type 1 diabetes in the United States, during a 15-month period, only 1 of 96 participants who had received three doses of BCG-Tokyo (given 2 to 3 years before) had Covid-19, as compared with 6 of 48 participants who received placebo.23

ial investigating the effect of BCG vaccination on glycemic control in patients with type 1 diabetes in the United States, during a 15-month period, only 1 of 96 participants who had received three doses of BCG-Tokyo (given 2 to 3 years before) had Covid-19, as compared with 6 of 48 participants who received placebo.23 The inconsistent results from these and other trials of the off-target effects of the BCG vaccine are probably explained by a number of factors, including differing study designs; varying age (infants, adults, and older adults), sex distribution, and proportion of participants who had previously received BCG vaccine; use of different BCG strains (with varying CFUs or dose)28,29 and number of doses; and different periods before pathogen exposure. All these factors warrant further investigation. BCG-induced effects might also vary among pathogens. In an animal model, BCG vaccination significantly reduced morbidity and mortality associated with influenza virus but not SARS-CoV-2 infection.25 In a randomized, controlled trial of neonatal BCG vaccination, in vitro immune responses varied according to pathogen type.30 Furthermore, in contrast to previously observed BCG-induced enhancement of in vitro cytokine responses to unrelated pathogens,31,32 responses to SARS-CoV-2 are decreased by BCG vaccination in adults.33 Factors that could have influenced off-target effects of the BCG vaccine in our trial include the predominance of female participants (in whom off-target effects are proposed to differ as compared with males)34 and the underrepresentation of participants who had not previously received the BCG vaccine.

ion in adults.33 Factors that could have influenced off-target effects of the BCG vaccine in our trial include the predominance of female participants (in whom off-target effects are proposed to differ as compared with males)34 and the underrepresentation of participants who had not previously received the BCG vaccine. Off-target effects of the BCG vaccine are proposed to, at least in part, be underpinned by epigenetic modifications in immune cells that induce a proinflammatory state and stronger cytokine responses to subsequent challenge with unrelated pathogens.31,32 Stronger immune responses can be beneficial to clear infections but might also increase symptoms. In a human malaria challenge model, participants who received the BCG-Bulgaria vaccine had an earlier onset of symptoms and overall more severe clinical symptoms than unvaccinated controls.35 In theory, an increased risk of symptomatic Covid-19 could be explained by a BCG-induced stronger immune response. BCG-vaccinated participants in the BRACE trial had more activated and effector T cells in response to in vitro SARS-CoV-2 stimulation than controls.33 These effects might result in more rapid clearance of SARS-CoV-2, leading to a shorter illness. There was some evidence of this in our trial in post hoc subgroup analyses: the duration of symptoms was lower in the BCG group than in the placebo group, although this finding was limited to participants 60 years of age or older and those without coexisting conditions.

ance of SARS-CoV-2, leading to a shorter illness. There was some evidence of this in our trial in post hoc subgroup analyses: the duration of symptoms was lower in the BCG group than in the placebo group, although this finding was limited to participants 60 years of age or older and those without coexisting conditions. In our trial, more than three quarters of the participants had previously received the BCG vaccine. It has been proposed that the off-target effects of BCG vaccination might be greater in those who have previously received the vaccine than in those who have not.36 However, it is also possible that revaccination does not induce any incremental off-target benefit over that provided by previous BCG vaccination.37 It is interesting that in our trial, there was weak evidence of a higher incidence of severe Covid-19 in the BCG group than in the placebo group among participants who had not previously received the BCG vaccine but not among those who received BCG revaccination. Our trial has several strengths. These include its robust design, large size, recruitment in 36 sites across three continents, blinding of trial-group assignments, stringent Covid-19 case definitions, close active follow-up of participants with daily data collection during illnesses, serologic tests every 3 months, a 98% follow-up rate, and a statistical analysis that accounted for Covid-19–specific vaccination.

sites across three continents, blinding of trial-group assignments, stringent Covid-19 case definitions, close active follow-up of participants with daily data collection during illnesses, serologic tests every 3 months, a 98% follow-up rate, and a statistical analysis that accounted for Covid-19–specific vaccination. The main limitations of our trial were the inability to recruit the planned sample and reduced participant observation time for the primary analysis resulting from the earlier-than-expected availability of Covid-19–specific vaccines. This means that the trial was underpowered and susceptible to type II error, and therefore it is possible that BCG vaccine increases the risk of Covid-19. Another limitation is that the trial definition of severe Covid-19 differed from that more widely used in Covid-19 studies, which commonly includes only hospitalization and death. More than 90% of participants who were categorized as having severe Covid-19 were captured solely by virtue of being “too sick to go to work” (71%) or “unable to get out of bed” (22%) for at least 3 consecutive days. The effect on severe Covid-19 as more commonly defined by hospitalization or death could not be meaningfully analyzed owing to the infrequency of these events. The possibility that BCG vaccine induces a stronger immune response that leads to more symptomatic disease but more rapid clearance of SARS-CoV-2 and consequent reduced hospitalizations and deaths therefore could not be assessed. Another limitation was that our definition of symptomatic Covid-19 was limited to the original case definition that did not include nonfebrile episodes without respiratory symptoms. Finally, blinding is a challenge in BCG trials, even with a placebo, owing to the injection-site reaction that develops in most persons. This limitation was mitigated by informing participants that BCG vaccination does not always cause a reaction (so that trial-group assignment could not be inferred from the absence of a reaction or scar), using objective primary outcomes, and blinding with respect to data collection and analysis. However, participant presumption of trial group might have influenced adherence to Covid-19 control measures, decisions to receive influenza or Covid-19–specific vaccines, participant reporting of symptoms, or SARS-CoV-2 testing.

ing objective primary outcomes, and blinding with respect to data collection and analysis. However, participant presumption of trial group might have influenced adherence to Covid-19 control measures, decisions to receive influenza or Covid-19–specific vaccines, participant reporting of symptoms, or SARS-CoV-2 testing. In this trial, BCG-Denmark vaccination did not reduce the risk of Covid-19 in health care workers, and the results did not exclude the possibility of an increased risk. Any effect on severe disease as defined by hospitalization or death could not be assessed. It is important that our findings are not extrapolated beyond the effect of BCG-Denmark vaccine on Covid-19 in health care workers. Several studies show beneficial off-target effects of the BCG vaccine in other situations, particularly among infants in high-mortality geographic settings,4 and ongoing research is examining potential underlying immunologic mechanisms.38,39