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Rationale for Randomized Clinical Trials Investigating the Potential of BCG Vaccination in Preventing COVID-19 Infection


Despite the implementation of mitigation measures, Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is still spreading worldwide, and has caused more than 1 million deaths so far. Although recent reports indicate that three vaccine candidates are effective against SARS-CoV-2, more time is needed to generate enough doses for the general population. Meanwhile, frontline healthcare workers are at high risk of SARS-CoV-2 exposure. To avoid collapse of the medical care system, there is a need to develop novel approaches to limit SARS-CoV-2 spread. Through a process called trained immunity, the Bacillus Calmette-Guerin (BCG) vaccine boosts the action of innate immune cells, resulting in a nonspecific reduction in the incidence of viral infections. Due to this immunomodulatory action, the BCG vaccine is currently used as a therapeutic in bladder cancer. Data collected from epidemiological and observational studies indicate that BCG vaccination might provide protection against COVID-19. While these observations do not provide evidence of causality and are limited by cofounding and intrinsic biases, it is crucial to explore the hypothesis that BCG vaccination may provide a nonspecific innate immune boost and therefore protect against COVID-19 in randomized controlled clinical trials, particularly for people at higher risk of developing COVID-19, such as frontline healthcare workers.


Coronavirus disease-2019 (COVID-19), caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first reported in December 2019 in Wuhan, China. SARS-CoV-2 is a beta-coronavirus closely related to SARS-associated coronavirus (SARS-CoV) and Middle Eastern Respiratory Syndrome (MERS-CoV) [1], and primarily targets the respiratory tract, causing disease ranging from common cold symptoms to a severe and fatal respiratory illness [2]. SARS-CoV-2 is highly transmissible and spreads via respiratory droplets or aerosols [3]. The most common COVID-19 clinical symptoms are fever, dry cough, loss of taste or smell, breathing difficulties and diarrhea [4]. Although the majority of SARS-CoV-2 infected individuals develop a mild disease, approximately 15 to 20% progress to a severe form of COVID-19 characterized by lung tissue damage, dyspnea, hypoxemia, respiratory failure and even death [4, 5]. Elderly people as well as individuals with comorbidities and underlying diseases such as cardiovascular disease, diabetes, liver disease, kidney disease, or cancer are at higher risk of developing severe COVID-19 [4, 6, 7]. Severe COVID-19 is characterized by overactivation of the immune system and extensive release of proinflammatory cytokines, a process called cytokine storm, which results in a multisystem inflammatory syndrome, fatal in 28% of cases [2, 8]. Children are less affected by COVID-19, with the majority of SARS-CoV-2 infected children developing mild or no symptoms [9]. However, in rare occurrences, some infected children develop a multisystem inflammatory syndrome (MIS-C) characterized by fever, severe abdominal pain, diarrhea, myocardial dysfunction, and cardiogenic shock, which requires intensive care treatment [10–15].

Despite the implementation of public health measures aiming to reduce and mitigate the spread of SARS-CoV-2 in the most affected regions, as of mid-January 2021, the COVID-19 pandemic has affected more than 95 million individuals and resulted in more than 2 million deaths worldwide [16]. Since early January 2020, when the genetic sequence of SARS-CoV-2 was characterized, multiple efforts have been underway to develop specific vaccines against the virus [17]. Although promising results have emerged for three vaccines candidates (BNT162b2 vaccine from Pfizer/BioNTech, mRNA-1273 from Moderna and AZD1222 from AstraZeneca), additional time will be required to mass produce and globally distribute these vaccines. Hence, other preventive treatments are urgently needed to decrease the risk of SARS-CoV-2 infection in individuals experiencing high levels of exposure, such as healthcare workers, first responders, and essential workers, as well as those in high-risk groups, such as individuals over 65 years of age and those with comorbidities.

Bacillus Calmette-Guérin (BCG) is a live attenuated vaccine originally developed 100 years ago against Mycobacterium tuberculosis, and is currently used worldwide in newborns and infants to prevent tuberculosis. By modulating the phenotype and function of innate immune cells and promoting an innate immune memory, a process called trained immunity, BCG vaccine induces potent protection against other infectious agents (Fig. 1) [18]. Administration of BCG vaccination shortly after birth decreases child mortality, mainly as a result of reduced neonatal sepsis, fever and respiratory infections [19–21]. BCG-induced trained innate immune cells respond more rapidly and efficiently to secondary, non-related, stimuli. Exploiting nonspecific boosting of innate immunity through BCG vaccination might be a valuable preventive and protective strategy during the current pandemic, as BCG vaccine might partially or completely decrease SARS-CoV-2 infections and reduce the severity of COVID-19 (Fig. 1) [22, 23]. Epidemiological reports do indicate a possible negative correlation between COVID-19 mortality rates and BCG vaccination coverage [24–26], and observational studies associated BCG vaccination with decreased rates of SARS-CoV-2 infections [27–29]. BCG vaccination is safe, immunogenic, inexpensive and already available. However, before starting mass BCG vaccination, randomized clinical trials are required to determine its safety and efficacy as a first-line preventive therapy for COVID-19.

Fig. 1

How BCG-induced trained immunity could prevent SARS-CoV-2 infections. Bacillus Calmette-Guérin (BCG) vaccination or other microbial components can induce a heterologous immunological memory, a process defined as “trained immunity”, which results in heightened innate immune responses upon exposure to secondary infections. BCG vaccination will initially stimulate innate immune cells, such as monocytes, macrophages, NK cells and neutrophils, and induce long-term metabolic and epigenetic reprograming resulting in increased responsiveness upon secondary stimulation with either the same or a different microbial ligand. In the context of COVID-19 pandemic, boosting innate immune cells by BCG vaccination and induction of trained immunity might provide nonspecific cross-protection against SARS-CoV-2 infection. Figure created with

How BCG-induced trained immunity could prevent SARS-CoV-2 infections. Bacillus Calmette-Guérin (BCG) vaccination or other microbial components can induce a heterologous immunological memory, a process defined as “trained immunity”, which results in heightened innate immune responses upon exposure to secondary infections. BCG vaccination will initially stimulate innate immune cells, such as monocytes, macrophages, NK cells and neutrophils, and induce long-term metabolic and epigenetic reprograming resulting in increased responsiveness upon secondary stimulation with either the same or a different microbial ligand. In the context of COVID-19 pandemic, boosting innate immune cells by BCG vaccination and induction of trained immunity might provide nonspecific cross-protection against SARS-CoV-2 infection. Figure created with

Nonspecific immune boosting and protective effects of BCG vaccination

While BCG vaccination is effective against tuberculosis in children, its protective effects appear reduced and less effective in older individuals [30]. Clinical evidence strongly indicates that BCG vaccination beneficially and nonspecifically alters the host immune response to confer protection against unrelated infections. The first report of nonspecific immunity induced by BCG vaccination dates back from 1927, when a 2- to 3-fold decrease in all-cause mortality was observed among Swedish children who received the BCG vaccination at birth, compared with unvaccinated children [31]. This steep decrease of mortality rate could not be explained by a BCG-targeted effect against tuberculosis alone, as the protection was extended to many other respiratory illnesses and diarrheal diseases, and was more likely mediated by a BCG-induced nonspecific immunity and protection from other unrelated bacterial and viral diseases [31, 32]. Observational studies and randomized trials in West Africa further confirmed this observation, where BCG vaccination at birth significantly reduced neonatal mortality by decreasing the incidence of respiratory infections, neonatal sepsis, and fever [19, 20, 33]. Additionally, a systematic review of 34 birth cohorts indicated lower risks of all-cause childhood mortality with BCG vaccination [34], and health survey data collected in low- and middle-income countries supports the protective role of BCG vaccination and its association with decreased risk of acute lower respiratory tract infections [35]. The nonspecific protective effects mediated by BCG vaccination, also called “off-target” or “heterologous” effects, are not only limited to infants and children, and a recent study showed a 75% decrease in the incidence of upper respiratory tract infections in adolescents revaccinated with BCG compared to placebo [36]. In a randomized placebo-controlled human challenge study, BCG vaccination improved the anti-viral response against a vaccine strain of yellow fever, as demonstrated by decreased viremia in BCG-vaccinated participants [37]. This BCG-induced anti-viral response was mediated by trained immunity, characterized by epigenetic reprograming of circulating monocytes and upregulation of their IL-1β production upon restimulation, which correlated with viremia reduction [37].

One application of the nonspecific heterologous immunomodulatory properties of BCG vaccination is in the treatment of cancer, and the potential of BCG to prevent tumor growth has been investigated in various experimental animal models [38, 39]. In a 60 year follow up of a BCG vaccination clinical trial, childhood BCG vaccination was associated with lower rates of lung cancer development [40], supporting the concept that early-life BCG vaccination might confer protection against cancer development later in life. BCG is also used therapeutically to treat cutaneous melanoma metastases, and BCG intralesional treatment induces regression of up to 90% of injected melanoma skin lesions and 17% of non-injected lesions [41, 42]. This effect appears to be mediated by trained immunity, as intralesional BCG induces transcriptional reprograming of melanoma skin lesions macrophages, improvement of their pro-inflammatory functions, and enhanced capacity to promote T cell activity in the tumoral microenvironment [43]. Intravesical instillation of BCG is also used as a nonspecific adjuvant in the treatment of non-muscle invasive bladder cancer and has been shown to delay disease progression and reduce disease recurrence [44–46]. This treatment is associated with increased immune cell infiltration in the bladder, as well as heightened urinary concentrations of pro-inflammatory cytokines and chemokines, which are typically associated with the trained immunity process [44].

BCG vaccination also appears to be beneficial in preventing Alzheimer’s disease, as a retrospective study indicates decreased risk of developing Alzheimer’s disease in patients with bladder cancer treated with BCG intravesical instillations [47]. Although the immune mechanisms involved in this protective effect still need to be characterized, it has been shown that BCG immunization decreases cognitive dysfunction and neuroinflammation in a transgenic murine model of Alzheimer’s disease, associated with the recruitment of inflammation-resolving macrophages to brain tissues [48].

Immune mechanisms involved in BCG-induced trained immunity

Trained immunity can be triggered by a primary infection or vaccination, is regulated by epigenetic and metabolic modifications, and results in long-term functional reprograming of innate immune cells (Fig. 1) [18, 49]. This functional reprogramming enhances the ability of innate immune cells to efficiently respond upon secondary stimulation by microbial pathogens, and eliminate the infection independently of T and B cells [18, 49]. By enhancing nonspecific immune resistance to reinfection, trained immunity also provides cross-protection against different pathogens.

Evidence of BCG-induced trained immunity has been demonstrated in murine models. For example, mice vaccinated with BCG are protected against secondary infection with either Candida albicans or Schistosoma mansoni [50, 51]. This effect does not rely on the adaptive immune system, as severe combined immunodeficiency (SCID) mice, which lack T and B cells, are still protected from secondary candidiasis [52]. Trained immunity has been described in various innate immune cell subsets, such as macrophages, monocytes, natural killer (NK) cells and neutrophils [18, 49, 53]. Indeed, peripheral blood mononuclear cells (PBMCs) collected from BCG-vaccinated healthy volunteers and stimulated ex vivo with an unrelated pathogen demonstrate increased production of pro-inflammatory cytokines, such as IFN-γ, IL-1β and TNF-α, up to 3 months post-BCG vaccination [52]. This response is mediated by epigenetic changes at the level of histone methylation (Histone H3 lysine 4, H3K4), which result in increased transcription of proinflammatory cytokines genes and long-term modulation of circulating monocytes [52]. Trained immunity also acts on NK cells; circulating NK cells isolated from BCG-vaccinated individuals demonstrate increased production of pro-inflammatory cytokines after ex vivo stimulation with either mycobacteria or an unrelated pathogen [54]. Furthermore, the nonspecific protection of BCG-vaccinated SCID mice against candidiasis is partially mediated by NK cell activity [54]. BCG vaccination also induces long-lasting phenotypic and functional reprograming of human circulating neutrophils, characterized by increased expression of activation markers and antimicrobial functions [53]. This reprogramming has been observed up to 3 months post-BCG vaccination [53].

Trained immunity is the main immunological mechanism by which BCG vaccination exerts its nonspecific cross-protection against other infectious agents. Therefore, through trained immunity, the BCG vaccine could potentially be used to help prevent epidemics, such as COVID-19, while specific vaccines are under development.

Epidemiological studies hinting the protective effect of BCG vaccine for SARS-CoV-2 infections

The decrease in tuberculosis incidence in developed countries has resulted in the application of different guidelines regarding BCG vaccination from one country to another. In some areas BCG vaccination is still part of a current national vaccination policy, in others BCG was once administered broadly but is now only given to specific groups of high risk individuals, and in some countries BCG has never been part of a vaccination policy [55]. Since BCG vaccination confers some nonspecific cross-protection against respiratory infections, it was initially postulated that history of BCG vaccination might underlie some of the variability in COVID-19 infection and death rates from country to country. However, the results from recent epidemiological studies are variable, with some supporting and others refuting this hypothesis. For example, a study analyzing SARS-CoV-2 infection rates in a cohort of individuals born 3 years before or 3 years after the end of the Israeli universal BCG vaccination program found no difference in the rates of SARS-CoV-2 positivity, and concluded that childhood BCG vaccination does not prevent SARS-CoV-2 infection in adults [56]. When comparing BCG vaccination policies with COVID-19 mortality in individuals older than 65 years from middle-high and high-income countries, COVID-19-related death rate appears to be reduced in countries with a previous universal BCG vaccination policy [26]. In this study, which has not undergone peer review, the consideration of only high- and middle-income countries aimed to avoid biases in COVID-19 statistics, and is based on the assumption that the countries selected would provide reliable reports of COVID-19 associated death rate [26]. Indeed, epidemiological analysis of the potential beneficial effects of BCG vaccination against COVID-19 need to account for cofounding variables. The cumulative number of confirmed SARS-CoV-2 infections and COVID-19-related deaths reported in each country might be influenced by reporting bias, differential testing capacities, absence of testing for asymptomatic SARS-CoV-2 infected individuals, and different methods of assessing the number of COVID-19-related deaths [25].

After accounting for multiple cofounding factors in their analysis, including the level of urbanization, population density, age, access to education and medical care, Escobar et al. reported strong associations between BCG vaccination and reduced COVID-19 deaths [24]. In a separate study, by considering only the day-by-day increase of COVID-19 confirmed cases and deaths, comparing the growth rate between countries which had a BCG vaccination policies with those that did not, and controlling for different cofounding factors, Berg at al. demonstrated a significant effect of mandated BCG policies on the growth of the pandemic as well as COVID-19 spread and deaths [25]. In an observational retrospective analysis of healthcare workers from the Los Angeles area, we showed that compared with healthcare workers that were not non-BCG vaccinated, history of BCG vaccination was associated with decreased self-reports of COVID-19 related symptoms and reduced seroprevalence of anti-SARS-CoV-2 antibodies [29]. This beneficial effect against SARS-CoV-2 infection was only observed in those with history of BCG vaccination and was not associated with other types of vaccination, such as influenza, meningococcal and pneumococcal [29]. In a cross-sectional study of Indian healthcare workers, the seroprevalence of SARS-CoV-2 antibodies was also reduced in individuals that reported BCG vaccination during childhood [28]. Another retrospective study on COVID-19 patients from a Rhode Island hospital indicated that BCG vaccination is associated with decreased risk of hospital admission during the course of COVID-19 [27].

In summary, these retrospective analyses suggest that BCG vaccination might exert a protective effect against SARS-CoV-2 infection and decrease COVID-19 related mortality. However, these reports are observational, and they cannot demonstrate a causal relationship between BCG vaccination and decreased rate of SARS-CoV-2 infection and COVID-19 mortality. Another caveat is that these studies may not reveal the potential of BCG vaccine given acutely to prevent SARS-CoV-2 infection, as in most cases the study participants were vaccinated as children, so their trained immunity may have faded. Only results obtained from randomized clinical trials will provide clear evidence of whether BCG vaccination is beneficial against SARS-CoV-2 infection. This strategy may be the best suited to protect individuals at the highest risk, such elderly people and others with comorbidities, and those who face the greatest exposure, such as frontline healthcare workers.

BCG vaccine as a preventive treatment for SARS-CoV-2 infection

SARS-CoV-2 is spreading rapidly throughout the world, and as of December 2020 many countries are experiencing second and third waves of infections associated overwhelmed healthcare systems and elevated mortality due to COVID-19. Results from a prospective observational cohort study in the UK and USA indicate that, compared with the general population, frontline healthcare workers are at higher risk of SARS-CoV-2 exposure and at increased chances of testing positive for COVID-19 [57]. This risk is also influenced by other factors such the lack of adequate personal protective equipment, the clinical setting and the ethnic background of healthcare workers [57]. There is a need to continue SARS-CoV-2 mitigation efforts and to prevent infections among healthcare workers. However, since effective SARS-CoV-2 vaccines are currently not yet widely available, additional prevention strategies need to be developed. Observational and epidemiological studies hinting at a potential beneficial effect of BCG vaccination against SARS-CoV-2 infection warrant the development of clinical trials to test this strategy. There are currently 22 ongoing interventional randomized clinical trials worldwide designed to determine if BCG vaccination can prevent SARS-CoV-2 infection, the majority aiming to assess the benefits of BCG vaccination in healthcare workers or elderly individuals ( (Table 1).

Table 1

List of randomized clinical trials evaluating the capacity of BCG vaccine to prevent COVID-19 in elderly or healthcare workers. Data collected from as of January 20, 2021

NCT NumberPhasesTitleSponsorsEstimated Completion
NCT04475302Phase 3BCG Vaccine in Reducing Morbidity and Mortality in Elderly Individuals in COVID-19 HotspotsTuberculosis Research Centre, IndiaMay 2021
NCT04632537Phase 3BCG Vaccination to Prevent COVID-19 (NUEVA)Henry M. Jackson Foundation for the Advancement of Military Medicine, USAApril 2023
NCT04379336Phase 3BCG Vaccination for Healthcare Workers in COVID-19 PandemicTASK Applied Science, South Africa4/28/21
NCT04328441Phase 3Reducing Health Care Workers Absenteeism in Covid-19 Pandemic Through BCG Vaccine (BCG-CORONA)UMC Utrecht, Netherlands4/30/21
NCT04350931Phase 3Application of BCG Vaccine for Immune-prophylaxis Among Egyptian Healthcare Workers During the Pandemic of COVID-19Ain Shams University, Egypt12/1/20
NCT04417335Phase 4Reducing COVID-19 Related Hospital Admission in Elderly by BCG VaccinationRadboud University, NetherlandsMay 2021
NCT04534803Phase 3BCG Against Covid-19 for Prevention and Amelioration of Severity Trial (BAC to the PAST)Harvard Medical School, USA11/30/21
NCT04537663Phase 4Prevention of Respiratory Tract Infection and Covid-19 Through BCG Vaccination In Vulnerable Older Adults (BCG-PRIME)UMC Utrecht, NetherlandsApril 2021
NCT04327206Phase 3BCG Vaccination to Protect Healthcare Workers Against COVID-19 (BRACE)Murdoch Childrens Research Institute, Australia3/30/22
NCT04414267Phase 4Bacillus Calmette-guérin Vaccination to Prevent COVID-19 (ACTIVATE II)Hellenic Institute for the Study of Sepsis, Greece5/25/21
NCT04369794Phase 4COVID-19: BCG As Therapeutic Vaccine, Transmission Limitation, and Immunoglobulin Enhancement (BATTLE)University of Campinas, BrazilAugust 2023
NCT04641858Phase 4BCG to Reduce Absenteeism Among Health Care Workers During the COVID-19 Pandemic (EDCTP)University of Southern DenmarkMarch 2022
NCT04461379Phase 3Prevention, Efficacy and Safety of BCG Vaccine in COVID-19 Among Healthcare WorkersHospital Universitario Dr. Jose E. Gonzalez, Mexico1/1/21
NCT04373291Phase 3Using BCG Vaccine to Protect Health Care Workers in the COVID-19 PandemicBandim Health Project, University of Southern Denmark8/1/21
NCT04384549Phase 3Efficacy of BCG Vaccination in the Prevention of COVID19 Via the Strengthening of Innate Immunity in Health Care Workers (COVID-BCG)Assistance Publique - Hôpitaux de Paris, France2/20/21
NCT04542330Phase 3Using BCG to Protect Senior Citizens During the COVID-19 PandemicBandim Health Project, DenmarkMarch 2022
NCT04348370Phase 4BCG Vaccine for Health Care Workers as Defense Against COVID 19 (BADAS)Texas A&M University, USANovember 2021
NCT04439045Phase 3Efficacy and Safety of VPM1002 in Reducing SARS-CoV-2 (COVID-19) Infection Rate and Severity (COBRA)University Health Network, Toronto7/1/21
NCT04387409Phase 3Study to Assess VPM1002 in Reducing Healthcare Professionals’ Absenteeism in COVID-19 PandemicVakzine Projekt Management GmbH, Germany5/1/21
NCT04435379Phase 3Study to Assess VPM1002 in Reducing Hospital Admissions and/or Severe Respiratory Infectious Diseases in Elderly in COVID-19 PandemicVakzine Projekt Management GmbH, Germany9/30/21
NCT04659941Phase 2Use of BCG Vaccine as a Preventive Measure for COVID-19 in Health Care Workers (Pro-BCG)Universidade Federal do Rio de Janeiro, Brazil10/01/22
NCT04648800Phase 3Clinical Trial Evaluating the Effect of BCG Vaccination on the Incidence and Severity of SARS-CoV-2 Infections Among Healthcare Professionals During the COVID-19 Pandemic in Poland (Pandemic in Poland)Hanna Czajka - Medical Research Agency, PolandApril 2021

The clinical trials may also lead to a more detailed characterization of the immunological mechanisms involved in the nonspecific BCG protective effect against unrelated viral infections. Through trained immunity, the BCG vaccine may boost innate immune responses, resulting in reduced SARS-CoV-2 viremia, increased IL-1β production and faster viral elimination [22, 23]. By inducing epigenetic changes, BCG vaccination could also functionally reprogram mature human neutrophils and increase their expression of activation markers and their antimicrobial functions [53]. Patients with severe COVID-19 exhibit dysfunctional cytotoxic immune responses, as demonstrated by reduced numbers of circulating NK cells and CD8+ T cells [58, 59]. By boosting NK cell function and proinflammatory cytokine production, BCG vaccination might ameliorate the dysfunctional cytotoxic immune responses observed during COVID-19. Pre-existing T cells able to cross-react with SARS-CoV-2 have been identified in healthy individuals that were not previously exposed to SARS-CoV-2, likely due to previous exposures to other coronaviruses [60–63]. The effect of such pre-existing memory SARS-CoV-2 cross reactive T cells on COVID-19 remains to be elucidated, however those cells could potentially be involved in viremia control and promote a more rapid production of anti-SARS-CoV-2 antibodies [64]. An additional proposed mechanism suggests that the BCG vaccine also activates CD4+ T cells and production of IFN-γ [65], and interestingly, in silico computational studies identified a 9-amino acid sequence shared between BCG and SARS-CoV-2, indicating that BCG vaccination might also result in the induction of T cells capable to cross-react with SARS-CoV-2 [66].

BCG vaccination is considered safe, even in latently infected adults with prior infant BCG vaccination [36, 67, 68]. BCG vaccination is also safe in elderly individuals, as no difference in the rate of adverse effects and no increase in the levels of pro-inflammatory cytokines at steady-state were observed between the BCG-vaccinated and placebo group in the ACTIVATE clinical trial [69]. Promising results were reported from the interim analysis of the double-blind Phase III ACTIVATE clinical trial, which investigated the benefit of BCG vaccination against other non-tuberculosis infectious diseases on patients older than 65 years [69]. BCG vaccination in elderly individuals led to a strong reduction in the incidence of new respiratory tract infections, which appeared to be mediated by trained immunity, as cytokine production by PBMCs isolated from elderly BCG-vaccinated individuals when exposed to an unrelated stimulus [69].

BCG vaccination induces long-term metabolic changes and epigenetic reprograming of monocytes, macrophages and NK cells, which boost their antimicrobial responses and promote host resistance upon exposure to unrelated infectious agents [49]. However, non-infectious agents, such as microbial products or endogenous stimuli, can also improperly elicit trained immunity, amplify innate immune responses and detrimentally contribute to tissue damage and the development of certain inflammatory diseases [18, 70, 71]. COVID-19 development is linked to dysregulated immune responses, and in up to 20% of infected individuals, SARS-CoV-2 infection results in hyperinflammation associated with high levels of circulating inflammatory markers and excessive production of proinflammatory cytokines, which has been correlated with COVID-19 severity and death [72, 73]. Therefore, it might be possible that in the context of this COVID-19 pandemic, BCG vaccine could be deleterious by contributing to SARS-CoV-2-induced inflammatory responses. However, in a retrospective cohort study, recent BCG vaccination was shown to be safe during this COVID-19 pandemic, and associated with decreased incidence of sickness [74]. Moreover, in a large cohort of healthy volunteers, BCG vaccine boosted the capacity of innate immune cells to mount antimicrobial responses and inhibited systemic inflammation in a sex-dependent manner, as demonstrated by decreased levels of circulating inflammatory markers post-BCG vaccination [75]. These observations suggest that the BCG vaccine does not exacerbate the development of inflammatory diseases, and further support the use of BCG vaccination as a preventive strategy for COVID-19. However only safety monitoring and results obtained from the ongoing randomized clinical trials testing BCG vaccination on healthcare workers will confirm whether the effects of BCG-induced trained immunity on COVID-19 are beneficial or deleterious [76]. These trials are also needed to further characterize the immune mechanisms involved. The results will not only benefit this current COVID-19 pandemic but may also be leveraged during future pandemic events while specific vaccines are under development.

Another potential challenge encountered with utilizing BCG vaccination as a COVID-19 preventative is the production of BCG vaccines in sufficient quantities to meet demand. Halts in BCG production owing to manufacturing issues associated with higher demand have resulted in BCG vaccines shortages over the last decade [77, 78]. However, positive results from randomized clinical trials assessing the capacity of BCG vaccination to protect from COVID-19 in healthcare workers may also stimulate BCG manufacturers to increase production. Such an outcome would also benefit patients with non-tuberculosis diseases for which BCG is used therapeutically, such as cutaneous metastatic melanoma and non-muscle invasive bladder cancer.


The ideal SARS-CoV-2 vaccine candidate will need to be safe and effective. At this stage of the SARS-CoV-2 clinical trials, it is still unclear whether the vaccine candidates will confer long-term protection against COVID-19 and be effective in the elderly. Recent reports indicate that three SARS-CoV-2 vaccine candidates display greater than 90% efficacy (BNT162b2 vaccine from Pfizer/BioNTech, mRNA-1273 from Moderna. Recent studies indicates that the efficiency of this vaccine is <70% not 90%), however it is unclear when those vaccines will be available to the general public. BCG vaccination has been shown to induce nonspecific immunity against viral respiratory tract infections, and BCG is safe, available, immunogenic and inexpensive. Therefore, boosting innate immunity by BCG vaccination might provide protection against COVID-19 and support the healthcare system until a safe and effective specific SARS-CoV-2 vaccine is widely available. More than 22 clinical trials are currently underway to test the capacity of BCG vaccination to protect against COVID-19, some of which will release their results early 2021. It would be also interesting to investigate if patients with bladder cancer treated with intravesical BCG experience any protection against SARS-CoV-2 infection or reduced COVID-19 severity. These clinical trials are of high importance, as their results will determine not only the efficacy of BCG vaccination against non-tuberculosis infectious pathogens but will also determine if BCG vaccination would help boost the responses to the specific COVID-19 vaccines in specific populations, and if it could be used in the future as a first preventive measure for the next pandemic.


The authors have no acknowledgments.


The others report no funding.


M.N.R.: reviewed the literature, wrote and critically revised the manuscript. C.J.R.: reviewed the literature, wrote and critically revised the manuscript. M.A: reviewed the literature, wrote and critically revised the manuscript.


This study, as a literature review, is exempt from any requirement for Institutional Review Board approval.


MNR, CJR and MA have no conflicts of interest to report.



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