Bacillus Calmette–Guérin (BCG) is the most widely used vaccine worldwide and has been used to prevent tuberculosis for a century. BCG also stimulates an anti-tumour immune response, which urologists have harnessed for the treatment of non-muscle-invasive bladder cancer. A growing body of evidence indicates that BCG offers protection against various non-mycobacterial and viral infections. The non-specific effects of BCG occur via the induction of trained immunity and form the basis for the hypothesis that BCG vaccination could be used to protect against the severity of coronavirus disease 2019 (COVID-19). This Perspective article highlights key milestones in the 100-year history of BCG and projects its potential role in the COVID-19 pandemic.
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The Bacillus Calmette–Guérin (BCG) vaccine has been used since 1921 to prevent tuberculosis (TB) and is considered to be the world’s most widely used vaccine1. In 2002, an estimated 75% of the 130 million children born worldwide were vaccinated with BCG2. BCG is also an established anti-cancer immunotherapy and is used intravesically for intermediate-risk and high-risk non-muscle-invasive bladder cancer (NMIBC) to prevent recurrence and progression3.
The beginning of 2020 saw the outbreak of the coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)4. With a global death toll of more than 3 million at the time of writing (7 May 2021), the pandemic has placed extraordinary demands on health-care systems5. A growing body of evidence suggests that the benefits of BCG extend beyond uses in TB and bladder cancer, with vaccination offering additional protection against various unrelated pathogens, including those that cause non-mycobacterial and viral infections6,7,8,9,10,11,12,13,14,15. Indeed, emerging data suggest that these non-specific effects might be protective against COVID-19 (refs16,17,18,19,20), and several randomized controlled trials are underway to investigate this hypothesis (Table 1). Thus, the COVID-19 pandemic provides a timely opportunity for urologists to reflect on the past 100 years of BCG in clinical practice.
In this timeline Perspective, we review the origins of BCG, its mechanisms of action and contemporary evidence for its use in TB, non-mycobacterial diseases and bladder cancer. We also discuss the role and use of BCG in the COVID-19 era and implications of this use for the urological community.
Origins of BCG
Following the discovery of Mycobacterium tuberculosis as the causative organism in TB by Robert Koch in 1882, scientists raced to develop a vaccine as the TB epidemic peaked across industrialized European cities (Fig. 1). In 1908, Albert Calmette and Camille Guérin began working to develop an effective vaccination against TB at the Pasteur Institute in Lille, France. Using ‘lait Nocard’, a virulent strain of Mycobacterium bovis originating from a cow with tuberculous mastitis, the pair subcultured the organism every 3 weeks on a glycerinated beef-bile-potato medium. After 13 years and more than 200 passages, the organism was finally attenuated to a weakened non-virulent form. Calmette and Guérin gave their names to this strain of M. bovis and the resulting vaccine became known as BCG21.
In 1921, Benjamin Weill-Halle and Raymond Turpin orally administered the first BCG vaccine to a neonate whose mother had died from TB at the Charité Hospital in Paris. The baby experienced no side effects from the vaccine and did not develop TB, despite maternal exposure. Over the next 3 years, 217 Parisian children were successfully vaccinated against TB, and mass production of the BCG vaccine commenced at the Pasteur Institute. The League of Nations declared the vaccine safe for use in 1928 and vaccination programmes continued uneventfully until 1930, when what would later be known as the Lübeck disaster occurred, in which 72 neonates in Lübeck, Germany, died after receiving the BCG vaccination22. Although their deaths were later shown to be due to accidental contamination of vaccine preparations with a virulent strain of M. tuberculosis, BCG vaccination suffered a major setback and enthusiasm for its use rapidly waned. However, a resurgence of TB during World War II led to a return of widespread BCG vaccination and public trust in its safety was restored23.
In 1974, the WHO created the Expanded Programme on Immunization to ensure universal access of mothers and children to routinely recommended infant vaccines. Intradermal (ID) BCG vaccination at birth has been included in this programme since inception, resulting in more than 4 billion vaccines administered to date24.
BCG is no longer a single vaccine (Fig. 2). Calmette and Guérin’s original strain was distributed to several laboratories across the world, and a number of diverse daughter strains have evolved as a result of genetic variation during decades of in vitro passage25. The main genetic modification involved in the attenuation of the strain is the loss of the genomic region of difference 1 (RD1), which generated the earliest BCG substrains, including BCG Japan, Birkhaug, Sweden, Russia and Moreau. Subsequently, deletion of RD2 led to the late strains, including BCG Pasteur, Danish, Glaxo, Tice, Montreal (also known as Frappier) and Connaught. Although >20 genetically distinct BCG strains exist26, 5 strains currently account for >90% of the vaccines used worldwide: Pasteur 1173 P2, Danish 1331, Glaxo 1077 (derived from the Danish strain), Tokyo 172-1 and Russian BCG-I27. Other commonly used strains include the Montreal and Tice strains, the latter of which is the only strain available for intravesical use in patients with NMIBC in the USA following suspension of BCG-Connaught production by the FDA in 2011 after mould was discovered at the manufacturing facility. As the Connaught strain supplied a significant proportion of the global market, the end of its production has led to a worldwide BCG shortage28.
Observational studies suggest that various BCG vaccine strains might have different immunogenicity and adverse reaction profiles, with the Russian strain potentially associated with reduced scarification29,30,31,32,33. A 2019 randomized controlled trial comparing vaccination with the BCG-Denmark (Copenhagen 1331), BCG-Japan (Tokyo 172-1) and BCG-Russia (Russia BCG-I) strains in neonates in Guinea-Bissau found no difference in all-cause morbidity (BCG-Denmark versus BCG-Russia, hospitalization incidence rate ratio (IRR) 1.08 (95% CI 0.84–1.37); BCG-Japan versus BCG-Russia, IRR 1.15 (95% CI 0.93–1.43)) or mortality (BCG-Denmark versus BCG-Russia, mortality rate ratio 1.15 (95% CI 0.74–1.80); BCG-Japan versus BCG-Russia, mortality rate ratio 0.71 (95% CI 0.43–1.19)) among strains34. However, in keeping with other studies, BCG-Russia produced fewer scars than other strains (BCG-Denmark versus BCG-Russia, prevalence ratio (PR) 1.07 (95% CI 1.04–1.10); BCG-Japan versus BCG-Russia, PR 1.06 (95% CI 1.02–1.09)). Although the presence of a BCG vaccine scar does not predict susceptibility to TB26, these findings suggest that differences could exist in the immune response to different BCG strains. Further evidence supporting this hypothesis comes from a large randomized trial in 303,092 neonates in Hong Kong that showed that the risk of TB after vaccination with BCG-Pasteur was 45% (95% CI 22%–61%) less than the risk after vaccination with BCG-Glaxo35. Additionally, a cohort study in Kazakhstan showed differences between the efficacy of different strains: neonatal vaccination with BCG-Tokyo, BCG-Serbia and BCG-Russia was shown to reduce the risk of clinically diagnosed TB by 69% (95% CI 61–75%), 43% (95% CI 31–53%) and 22% (95% CI 7–35%), respectively36.
Whether strain selection influences the efficacy of intravesical BCG in treating NMIBC is unclear. Several different strains including BCG Tice, BCG Moreau, BCG Connaught and BCG Tokyo-172 with different quantities of colony-forming units are currently in use for intravesical instillations37. In a prospective randomized controlled trial comparing BCG Connaught with BCG Tice in 132 patients with high-risk NMIBC, 5-year recurrence-free survival was significantly higher in the BCG Connaught group (74% versus 48%, P = 0.0108), but progression-free survival (P = 0.3442) and overall survival (P = 0.2652) did not differ between the groups38. However, this study had several limitations, including a lack of maintenance treatment. A larger retrospective study comparing the same strains in 2,099 patients showed that BCG Connaught was more effective than BCG Tice for time-to-first recurrence (HR 1.48; 95% CI 1.20–1.82; P < 0.001)39. However, when maintenance BCG was used, the opposite was true (HR 0.66; 95% CI 0.47–0.93, P = 0.019). The authors hypothesize that this might be due to BCG Connaught reaching an earlier cumulative optimized dose than BCG Tice39. Subsequently, a 2020 retrospective comparison of BCG Tice (n = 321) with BCG Moreau (n = 339) showed no difference in recurrence-free (HR 0.88; 95% CI 0.56–1.38, P = 0.58) or progression-free survival (HR 0.55; 95% CI 0.25–1.21, P = 0.14)40. Likewise, a meta-analysis comparing nine strains across 65 trials was unable to demonstrate the superiority of one BCG strain over another at preventing recurrence41. Ultimately, comparative trials are needed to determine the effect of strain selection on BCG efficacy and to identify whether an optimal strain exists for treatment of NMIBC.
BCG and tuberculosis
TB is the leading infectious cause of death globally, responsible for an estimated 1.4 million deaths in 2019 (ref.42). In countries with a high incidence of TB (≥40 per 100000), BCG vaccination reduces the risk of childhood meningeal and miliary TB by 85%43 and pulmonary TB by 50%44. These protective effects last ~10–15 years, although a small number of studies have demonstrated protection of up to 50 years after vaccination45,46.
However, adults and adolescents, not children, are thought to be responsible for the majority of community transmission of TB47. The protective effect of BCG vaccination is far more variable in adolescents and adults than children, with protection rates ranging from 0–80%48. Reasons for this high variability are not clear, but could include differences in BCG strain, host genetics and previous exposure to environmental mycobacteria that can confer some underlying protection against M. tuberculosis49,50.
A vaccine that prevents pulmonary TB in adolescents and adults is, therefore, urgently needed for TB control. Fortunately, novel insights into the basic immunology of M. tuberculosis infection and clinical vaccine development have led to the development of potential vaccine candidates, some of which are now in advanced clinical trials. In particular, two phase IIb trials are worth highlighting. In a 2018 clinical trial of re-vaccination of adolescents in South Africa, a reduction in the rate of TB infection was observed in the BCG re-vaccinated groups (efficacy 45.4%, P = 0.03), as measured by the rate of sustained Quantiferon-TB Gold In-tube assay conversion, compared with participants who received a placebo vaccination (30.5%, P = 0.16)51. In a second 2018 trial, protection against TB could be achieved by vaccination of M. tuberculosis-infected adults with an adjuvanted subunit vaccine containing two M. tuberculosis proteins (efficacy 54%, 95% CI 13.9–75.4%; P = 0.04)52.
Interestingly, although intravenous (IV) BCG injections had been consigned to the history books, this approach was revisited in a 2020 study in adult rhesus macaques53. The study compared ID and IV injection of BCG and observed that IV BCG was highly effective in protecting against M. tuberculosis challenge, with six out of ten vaccinated animals showing no signs of infection as defined by lack of granuloma formation. Furthermore, nine out of ten IV BCG-immunized macaques had no signs of tuberculous disease, as determined by a lack of lung fluorodeoxyglucose activity at the time of necropsy. By contrast, no evidence of protection against infection or disease was seen in macaques receiving ID injection of the standard human dose. Although these results are encouraging, meticulous safety testing is required to prove that IV administration is safe in humans. As seen in the Lübeck disaster, direct IV injection of a contaminated vaccine could lead to fatal infection. Nevertheless, these studies represent milestones in the efforts to develop a novel TB vaccine that protects against both neonatal and adult TB.
Non-specific effects of BCG
A growing body of evidence indicates that vaccines have non-specific effects on the immune system54. Also known as heterologous or off-target effects, these afford additional protection beyond that offered against their target disease.
Over the past 50 years, numerous studies have proved that BCG vaccination is able to induce non-specific protective effects. Carl Naslund in Sweden first described this phenomenon in 1932, noting that BCG-vaccinated neonates (n = 1,323) had a mortality rate that was almost threefold lower than those who were unvaccinated (n = 3,350; 6.6% versus 22.2%)55. Subsequent epidemiological studies have corroborated this finding, showing a correlation between BCG vaccination and reduced childhood mortality56,57,58, and hospitalization rates attributable to other respiratory infections59, independent of its effect on TB.
Strong evidence for the non-specific effects of BCG vaccination comes from a series of randomized controlled trials in Guinea-Bissau, a country with a high childhood mortality rate58,60,61,62,63. The main study found that low-birth-weight neonates vaccinated at birth had a >40% reduction in neonatal mortality rate compared with low-birth-weight neonates who had delayed vaccination at 6 weeks62. This effect seems to be mainly due to protection against neonatal sepsis and respiratory infection61. Subsequently, the phase III ACTIVATE trial assessed whether BCG confers similar protective effects against respiratory infections in the elderly15. In this double-blind, randomized trial, 198 hospitalized elderly patients received either BCG or placebo vaccine at discharge and were followed up for 12 months for the occurrence of new infections. At interim analysis, BCG vaccination significantly increased the time to first infection compared with placebo (median 16 weeks versus 11 weeks; P = 0.039). The incidence of new infections was 42.3% (95% CI 31.9%–53.4%) after placebo vaccination compared with 25% (95% CI 16.4%–36.1%) after BCG vaccination; most of the protection in the BCG group was determined to be against respiratory tract infection of probable viral origin (HR 0.21, P = 0.013).
Evidence from murine models and human trials has shown that BCG vaccination protects against secondary infections with Candida albicans6,7, Schistosoma mansoni8 and Plasmodium9,10,11,12. In a randomized study, participants received either BCG or placebo vaccination followed by a trivalent seasonal influenza vaccine 14 days later13. The data showed that BCG-vaccinated subjects had markedly enhanced antibody responses against the A(H1N1)pdm09 vaccine strain compared with patients who had received placebo (0.041), with a trend towards more rapid seroconversion (P = 0.08). In another randomized placebo-controlled study, yellow fever vaccine recipients who had received the BCG vaccine 1 month previously had significantly lower yellow fever vaccine viraemia than subjects who had received previous placebo vaccination (P < 0.05)14. The lower vaccine viraemia was also accompanied by lower circulating inflammatory cytokines in BCG-vaccinated individuals — lower levels of circulating inflammatory cytokines were seen because the high cytokine production capacity following BCG vaccination leads to a rapid local antimicrobial response and subsequent elimination of the pathogen, thereby preventing a systemic reaction and high levels of circulating cytokines64,65. However, yellow fever antibody titres did not differ between placebo and BCG-vaccinated groups 90 days after receiving the vaccine, indicating that the trained immunity induced by BCG confers protection via an antigen-unspecific process66.
BCG vaccination has also been shown to have a protective effect against atopy measured by skin-test reactivity to three allergens, Dermatophagoides pteronyssinus, Dermatophagoides farinae and cockroach67. This finding has been validated in randomized controlled trials; one Dutch study of 121 newborns showed that BCG-vaccinated infants used significantly less medication for eczema than unvaccinated infants (P = 0.04)68. In the separate Dutch Calmette Study, neonatal BCG vaccination reduced the cumulative incidence of atopic dermatitis in children with atopic predisposition compared with BCG-unvaccinated predisposed infants (22.7% versus 25.4%; RR 0.90 (95% CI 0.8–1.0))69. Furthermore, in a clinical trial of BCG vaccination with a 60-year follow-up period, BCG-vaccinated children had a significantly reduced risk of lung cancer development than those who received placebo (18.2 versus 45.4 cases per 100,000 person-years; 95% CI 0.20–0.74, P = 0.05), even when controlling for other risk factors including smoking, sex, region and alcohol overuse70. Notably, however, the overall rate of cancer diagnosis was not significantly different in BCG vaccine versus placebo recipients (HR 0.82; 95% CI 0.66–1.02).
BCG and cancer
The concept of using microbial products as immunotherapy for cancer was pioneered by William B. Coley at the turn of the 20th Century. After learning about a patient with an inoperable malignant neck tumour that disappeared after developing erysipelas, Coley started treating his own patients with cancer with intratumoural injections of live Streptococcus pyogenes71 and, later, mixtures of S. pyogenes and Serratia marcescens72. Although he observed tumour regression in several patients, the injections had unpredictable efficacy and lethal adverse effects sometimes occurred.
In 1929, Raymond Pearl noted that patients with lesions of active TB had a lower frequency of cancer on post-mortem examination73, although he was unable to provide an explanation for this finding. In 1959, landmark studies by Lloyd Old at the Memorial Sloan-Kettering Institute in New York demonstrated the inhibition of cancer by BCG: mice infected with BCG showed increased resistance to the transplantation of the murine tumour cell lines S-180, carcinoma 755 and Ehrlich ascites74.
Further work published in 1971 by Zbar and Tanaka at the National Cancer Institute was instrumental in confirming the anti-neoplastic properties of BCG75. Zbar found that intralesional injection of BCG into guinea pigs induced regression of ID tumours, prevented the development of lymph node metastases and eradicated nodal micrometastases75. Zbar later went on to describe the four criteria for optimal BCG therapy: proximity between BCG and tumour cells, a small tumour burden, a host capable of mounting an immunological reaction to mycobacterial antigens, and sufficient numbers of viable mycobacteria76. This work led to the clinical use of BCG as cancer therapy, first in acute lymphoblastic leukaemia, in which adjuvant BCG reduced relapse rates77, and later in malignant melanoma in which skin lesions regressed following treatment with intralesional BCG injection78. These reports created a great deal of interest in BCG and prompted a number of clinical trials using BCG against kidney79, colon80 and lung81 cancer. Unfortunately, these trials failed to show a significant benefit of BCG in these tumour types, although, notably, most of the studies were in patients with advanced disease who, based on Zbar’s criteria, would not be expected to respond to BCG82.
BCG and bladder cancer
The most successful application of BCG for the treatment of malignancy was in NMIBC. Preliminary work by Coe and Feldman showed that BCG elicited a delayed hypersensitivity response in guinea pig bladders83, and when injected into a malignant melanoma metastasis in the bladder, complete eradication was observed84.
In the early 1970s, Alvaro Morales started investigating the use of BCG in bladder cancer and in 1972 devised the BCG protocol that remains in use today85. Interestingly, Morales chose the schedule of six weekly instillations simply because the Armand Frappier strain of BCG he was using was supplied in six separate vials with adverse events lasting less than 1 week85. In a landmark study in 1976, Morales treated nine patients with recurrent NMIBC with weekly intravesical and ID BCG for 6 weeks, observing a 12-fold reduction in bladder cancer recurrence (P < 0.01)85. These promising data prompted two randomized controlled trials testing the effectiveness of transurethral resection (TUR) followed by intravesical BCG for NMIBC versus surgical resection alone. In a 1980 study in 37 patients, BCG significantly reduced tumour recurrence rate compared with resection alone (17% versus 42%, P = 0.029)86. Similarly, a 1985 randomized trial of 86 patients with 43 in each treatment arm demonstrated a significant reduction in the number of recurrent tumours in patients receiving BCG compared with a control group receiving standard care (cystoscopy and fulguration) (43 versus 27 patients, respectively; P < 0.001)87. Furthermore, patients treated with BCG also demonstrated reduced tumour progression requiring cystectomy compared with patients in the control group (3 versus 15 patients, respectively, P < 0.001)87. Subsequent meta-analyses have confirmed that BCG is associated with a decreased risk of recurrence compared with TUR alone88,89. Han et al. analysed 4,767 patients undergoing TUR from 25 randomized controlled trials and found a significant difference in the odds ratio for tumour recurrence between groups treated with and without BCG (OR 0.61, 95% CI 0.46–0.80, P < 0.0001)89. BCG has also been shown to be superior to chemotherapy for recurrence prevention90,91,92. A meta-analysis of 2,749 patients from 11 randomized controlled trials reported that BCG was superior to mitomycin C in reducing tumour recurrence (OR 0.56, 95% CI 0.38–0.84, P = 0.005)90. Furthermore, in the subgroup treated with BCG maintenance, all six studies showed significant superiority of BCG over mitomycin C (OR 0.43, 95% CI 0.35–0.53, P < 0.001)90. Similarly, in a meta-analysis using individual patient data from nine randomized controlled trials (n = 2,820), Malmstrom and colleagues observed a 32% reduction in risk of recurrence in patients treated with maintenance BCG compared with those treated with mitomycin C (P < 0.0001)92. Patients treated without maintenance BCG demonstrated a 28% increase in recurrence risk (P = 0.006)92.
With regard to tumour progression, several meta-analyses have concluded that intravesical BCG prevents — or at least delays — progression to invasive disease93,94. The largest of these studies analysed 24 trials (n = 4,863 patients) and showed a 27% reduction in the odds of progression (9.8% versus 13.8%; OR 0.73, P = 0.001) in patients treated with maintenance BCG compared with either TUR alone or TUR with chemotherapeutic agents other than mitomycin C93. Notably, however, the Malmstrom meta-analysis was unable to confirm a significant difference between BCG and mitomycin C for either progression (P = 0.6164) or survival (P = 0.2783)92. These conflicting results could perhaps be explained by differences in patient characteristics, maintenance schedules, follow-up period and statistical power95.
Another area of controversy related to BCG therapy is the optimal duration of maintenance regimens. Although different regimens have been used, a 2002 meta-analysis was unable to determine which regimen was most effective for NMIBC treatment93. However, a 3-year maintenance schedule is supported by data from the SWOG 8507 (ref.96) and EORTC 30962 (ref.97) studies. SWOG 8507 showed that maintenance BCG given as a weekly instillation for 3 weeks over a 3-year period increased the 5-year recurrence-free survival from 41% to 60% (P < 0.0001) compared with induction BCG alone96. Accordingly, EORTC 30962 used a similar regimen and showed that 3 years of maintenance treatment reduced the recurrence rate compared with 1 year of BCG maintenance in patients with high-risk disease (95% CI 1.13–2.30; P = 0.009)97. As such, current European Association of Urology (EAU) and American Association of Urology(AUA)/Society of Urologic Oncology (SUO) guidelines recommend a risk-stratified schedule for maintenance therapy, such that patients with intermediate-risk disease should receive maintenance therapy for 1 year whereas patients with high-risk disease receive treatment for up to 3 years3,98.
Despite high success rates, BCG fails in approximately 25–45% of patients, with a further 40% of patients eventually relapsing despite an initial response96,99,100,101. Furthermore, intravesical BCG can cause adverse effects, which — although mild in the majority of cases — can be poorly tolerated and curtail treatment schedules102. Haematuria and cystitis are the most common local side effects occurring in approximately 20% and 35%, respectively, and tend to arise in the first 48 h after BCG instillation103. Systemic adverse effects include pyrexia, fatigue and general malaise. Severe systemic effects are rare (<1%) and are the result of disseminated infection (also known as BCG-osis), which can present as sepsis, reactive arthritis, pneumonitis, rash, or — rarely — mycotic aneurysm104,105,106.
Mechanisms of BCG in bladder cancer
The precise mechanism of action by which BCG immunotherapy exerts its effect remains incompletely elucidated. However, it is clear that BCG induces a robust immune response that leads to adaptive immunity and anti-tumour activity. Following intravesical instillation, BCG is believed to attach to and invade the urothelium. Although murine studies indicate that BCG binds to the urothelium via fibronectin receptors107, this mechanism of attachment is not supported by studies in humans108,109. Regardless, once BCG attaches to the urothelium, it is internalized by urothelial cells, bladder cancer cells and immune cells110. Internalization stimulates a local and systemic innate immune response leading to the release of several chemokines and cytokines including IL-6, IL-8, GM-CSF and TNF111,112,113. In fact, the release of these pro-inflammatory cytokines might be used to predict response to BCG therapy for bladder cancer. For example, the CyPRIT assay, a nomogram constructed using urinary levels of cytokines induced by BCG (IL-2, IL-6, IL-8, IL-18, IL-1RA, TRAIL, IFNγ, IL-12p70 and TNF), was able to predict the likelihood of recurrence with 85.5% accuracy (95% CI 77.9–93.1%)114. Following this cytokine and chemokine burst, cytotoxic immune cells, including neutrophils, monocytes, CD4+ and CD8+ T cells, B cells, macrophages and natural killer (NK) cells, are recruited. Immune-mediated cytotoxicity of bladder cancer cells subsequently occurs via activation of NK cells, T cells and secretion of soluble factors such as TRAIL by polymorphonuclear cells110.
The success of BCG therapy also depends on the induction of adaptive immunity110. BCG antigens are presented on the cell surface of antigen-presenting cells and urothelial cells via MHC class II. These molecules interact with CD4+ T cell receptors, leading to activation and differentiation of a primarily T helper 1 cell immune response110,115. Together, both innate and adaptive immune system responses lead to lasting protection against tumour recurrence and progression110.
BCG and trained immunity
The non-specific effects of BCG might be explained in part by trained immunity — the concept that innate immune cells (such as monocytes and macrophages) encountering a vaccine or microbial component can be trained by a primary stimulus to improve responsiveness to a similar or unrelated secondary stimulus113.
Host immune responses are divided into innate and adaptive responses and, until relatively recently, it was believed that only adaptive immunity possessed immunological memory116. However, studies over the past decade have shown that innate immune cells also possess intrinsic memory characteristics7,14,117 and can undergo functional reprogramming to enable an enhanced response to secondary stimulation (Fig. 3). This reprogramming is achieved through histone modifications, which are epigenetic alterations of the chromatin structure in the nucleus that result in enhanced chromatin accessibility, and facilitate transcription of genes important for antimicrobial responses and improved cell function118. Additionally, metabolic changes such as increased glycolysis, oxidative phosphorylation and glucose consumption lead to selective accumulation or depletion of certain metabolites, such as glutamate and malate, that regulate this process119.
BCG vaccination is able to endow circulating monocytes with characteristics of trained immunity through epigenetic and metabolic rewiring of myeloid progenitors in the bone marrow120,121. This process begins with autophagy, the process of intracellular degradation of cell and microbial components. Phagosomal digestion of BCG causes the release of muramyl dipeptide (MDP) as well as metabolic changes through activation of the Akt-mTOR-HIFα pathway122. MDP binds to nucleotide-binding oligomerization domain-containing protein 2 (NOD2) receptor to induce epigenetic histone alterations7. Epigenetic modifications result in increased access to the promoter regions of genes related to inflammatory pathways, such as cytokines and pattern recognition receptors. As a result, these BCG-trained innate immune cells express higher levels of pattern recognition receptors and produce increased levels of pro-inflammatory cytokines than non-BCG-trained cells when challenged by a secondary and potentially unrelated stimulus7,14, thus increasing the capacity of the innate immune cells to mount a faster and augmented response to such a secondary stimulation.
Emerging data have identified a key role for the stimulator of interferon genes (STING) pathway in mediating innate immune responses123,124. STING is a cytosolic receptor, and activation of STING induces potent cytokine and cellular immune responses against microbial infection123. STING-dependent signalling is activated by binding cyclic dinucleotides either secreted by intracellular bacteria or distinct host cyclic dinucleotides generated by host cell receptors after recognition of cytosolic double-stranded DNA125,126,127. STING agonists might, therefore, be a novel class of vaccine adjuvants capable of inducing cellular immune responses and protective efficacy against intracellular pathogens. Studies of a recombinant BCG that released high levels of STING agonist demonstrated a significantly augmented pro-inflammatory cytokine response (TNF, IL-6 (P < 0.05); IL-1β (P < 0.001)) in vitro in murine macrophages challenged with M. tuberculosis128. Attenuation of M. bovis for clinical use as BCG results in the loss of the early secretory antigenic target system (ESX-1), which is critical for activation of the STING pathway129. This loss potentially limits subsequent BCG responsiveness owing to reduced induction of immune cell-recruiting chemokines. To compensate, several recombinant versions of the BCG vaccine have been produced. One example is the VPM1002 vaccine, which activates the STING pathway and has been shown to be potentially more immunogenic than conventional BCG: in a phase II trial with a 6-month follow-up, 48 HIV-unexposed newborn infants were vaccinated with either VPM1002 (n = 36) or BCG Danish strain (n = 12)130. Although both vaccines induced IL-17 responses, VPM1002 vaccination led to a significant increase in CD8+IL-17+ T cells at day 14 (P = 0.0156) and month 6 (P = 0.0002) compared with BCG130. Trials are currently investigating whether VPM1002 can protect health-care workers131,132 and the elderly133 against severe COVID-19 (Table 1).
Trained immunity and bladder cancer
Trained immunity might also have a role in the effect of intravesical BCG for NMIBC as an anti-tumour mechanism66. This role is not well defined; data on epigenetic modifications in innate immune cells during intravesical BCG instillations are lacking. However, increased cytokine134,135,136 and chemokine137,138 production by innate immune cells during intravesical BCG therapy is well described and might indirectly support a role for trained immunity in the mechanisms of BCG immunotherapy for NMIBC.
Further support for the role of trained immunity comes from studies evaluating the role of recombinant BCG and STING agonists in bladder cancer. The STING signalling pathway not only mediates innate immune responses against microbial infection but is also important for the anti-cancer immune response. Activation of the STING signalling pathway by tumour-derived DNA results in production of type I interferon and other pro-inflammatory cytokines that stimulate cross-presentation of tumour antigens and mobilization of tumour-specific CD8+ T cells126. Thus, STING agonists have the potential to induce an anti-tumour immune response. Studies have evaluated the effect of BCG in combination with a STING agonist in cell-line models representing human monocytes, the bladder cancer cell line RT112 and primary bladder epithelial cells139. They showed a >20-fold increase in immune cell recruiting chemokines including CXCL10 as a result of synergistic effect of BCG and the STING agonist139. In another study, use of a recombinant BCG strain overexpressing a STING agonist stimulated epigenetic changes that promoted enhanced anti-tumour immunity compared with wild-type BCG in rat NMIBC tumour models140. A significantly reduced number of immunosuppressive M2 macrophages and increased pro-inflammatory M1 macrophages (P < 0.01) was observed with the recombinant BCG strain compared with wild-type BCG. Additionally, myeloid cells treated with the recombinant BCG strain exhibited enhanced phagocytosis and autophagy to a greater degree than wild-type BCG. These findings highlight the improved ability of BCG to elicit trained immunity when combined with a STING agonist.
BCG in the COVID-19 era
The COVID-19 pandemic is a public health crisis caused by infection with SARS-CoV-2. COVID-19 has reached at least 212 countries and territories, with a global death toll of more than 3 million at the time of writing (7 May 2021)5. The outbreak of COVID-19 has placed extraordinary demands on health-care systems whilst also triggering a global recession that is set to exceed that of the 2008 financial crisis141,142. Furthermore, the pandemic is predicted to last ~2 years, with further waves of infection occurring during winter or when quarantine regulations are relaxed143.
The pandemic has transformed cancer care, including that of patients with high-risk NMIBC. In particular, urologists must balance patients’ risk of acquiring COVID-19 as a result of hospital visits for intravesical BCG instillations with the risks of recurrence and/or progression due to deferred treatment. Data show that people over the age of 65 years are at an increased risk of developing acute respiratory distress syndrome after contracting COVID-19 (HR 3.26; 95% CI 2.08–5.11)144; the majority of patients with high-risk NMIBC fall into this age group and should, therefore, be regarded as an at-risk demographic145.
Several expert panels have produced recommendations for the use of intravesical BCG during the pandemic (Fig. 4). All agree that patients with high-risk NMIBC should receive induction BCG146,147 because the risk of recurrence and progression can be reduced by up to 70% and 26%, respectively91,93. With regard to maintenance BCG, attempts should be made to provide patients with at least the first 3-week maintenance regimen and at least two out of the three doses of a maintenance course are acceptable in order to minimize the number of hospital visits147. For those patients who have completed more than a year of maintenance therapy, further doses can be safely discontinued148. When managing BCG-related adverse effects, urologists should have a low threshold for testing pyrexial patients for COVID-19 (ref.147).
COVID-19 and BCG vaccination
Given the non-specific protective effects of BCG vaccination against viral infection, these benefits have been hypothesized to extend to protection against COVID-19 through the induction of trained immunity.
Several ecological studies have proposed a correlation between BCG vaccination policies and COVID-19-related mortality and morbidity16,17,18,19. For instance, countries with a BCG vaccination programme for TB had a lower daily incidence of COVID-19 (0.8 per million) than countries without such a programme (34.8 per million)16. Furthermore, both mortality and crude case fatality rate were lower in countries with a BCG vaccination programme compared with those without (0.08 per million and 4.1% versus 34.8 per million and 5.1% respectively). Similarly, the presence of mandatory national polices for universal BCG vaccination was associated with flattened growth curves for confirmed cases of COVID-19 and resulting deaths in the first 30-day period of country-wise outbreaks17. Overall, countries including BCG in their national vaccination programmes had a significantly lower incidence of COVID-19 cases (mean cases per population ratio: 0.0147 ± 0.027 versus 0.1892 ± 0.244, P < 0.0001) and mortality (mean of deaths per population ratio: 0.0004 ± 0.001 versus 0.0113 ± 0.020, P < 0.0001) than countries that excluded it18. Subsequently, an assessment of the global linkage between BCG vaccination and COVID-19 mortality19 showed a strong correlation between the BCG index (an estimation of the degree of universal BCG vaccination deployment in a country) and COVID-19 mortality (r2 = 0.99, P = 8 × 10−7), indicating that every 10% increase in the BCG index was associated with a 10.4% reduction in COVID-19 mortality.
Although intriguing, these findings must be interpreted with caution, as ecological studies carry inherent limitations. First, any risk reduction seen as a result of BCG vaccination applies to a population rather than an individual. Second, these studies are susceptible to bias from confounders such as differences in national demographics, reporting biases, testing rates for COVID-19 and the stage of the pandemic in each country. For example, an analysis of the COVID-19 spread rate in 74 countries stratified according to BCG vaccination policy (no policy, past universal vaccination policy or current universal policy)149 reported that, although a lower COVID-19 spread rate and mortality was observed in countries with a current universal vaccination policy compared with countries with no or prior universal vaccination policy, adjusting for COVID-19 testing rates meant that those countries with high testing rates (defined as 10 or more tests per thousand inhabitants) no longer showed a significant association between BCG policy and COVID-19 spread rate. Accordingly, in a study of Israeli adults aged 35–41 years with COVID-19-compatible symptoms, individuals born during a period of universal BCG vaccination had similar rates of positive COVID-19 test results to those who were born after cessation of universal vaccination (11.7% versus 10.4%, 95% CI −0.3–2.9%; P = 0.09)150. Likewise, a preliminary study was unable to demonstrate an association between COVID-19 case fatality and BCG vaccination before 1980 (P = 0.258) or with year of establishment of universal vaccination (P = 0.852)151. Several other studies have also failed to demonstrate a correlation between vaccination policy and SARS-CoV-2 infection152,153,154.
A 2021 study has attempted to reconcile the conflicting findings from different studies regarding protection of BCG against COVID-19 (ref.155). By modelling the effect of BCG vaccination across different times during the pandemic the authors show that the protective effect of BCG vaccination against COVID-19 is strongest during the early stages of the pandemic. This protection gradually dissipates in later stages as governments introduce social distancing and other preventative measures.
Although results from ecological studies are conflicting, clinical data to support the hypothesis that BCG offers protection against COVID-19 are emerging. In a retrospective study, volunteers who received the BCG vaccine within the past 5 years had a lower incidence of self-reported sickness (20.7% versus 31.1%, P < 0.05) and extreme fatigue (8.3% versus 18.9%, P < 0.01) during the COVID-19 pandemic compared with those who had never received the vaccine156. Data from 120 consecutive adult patients with COVID-19 from a predominantly Latino and Hispanic population receiving care at a major federally qualified health centre demonstrated that BCG-vaccinated patients were less likely to require hospital admission during the disease course than non-BCG-vaccinated individuals (3.7% vs 15.8%, P = 0.019). This association remained unchanged after adjusting for demographics and comorbidities (P = 0.017) using multivariate regression analysis157. Accordingly, a study that assessed morbidity due to SARS-CoV-2 infections in a large cohort of health-care professionals from a multi-site Los Angeles health-care organization20 reported that almost 30% of the study participants had a history of BCG vaccination, and that BCG vaccination was associated with a decrease in self-reported COVID-19 diagnoses (1.9% versus 2.9%; P = 0.029), reduced seroprevalence of anti-SARS-CoV-2 IgG (2.7% versus 3.8%; P = 0.044) and a decrease in COVID-19-specific symptoms (75.6% versus 72.7%; P = 0.017).
Ultimately, these findings need confirmation and phase III–IV trials are currently underway to establish whether BCG vaccination of health-care workers and the elderly could protect them from COVID-19 (Table 1). If proved effective, BCG vaccines could be repurposed to provide a rapid response to the pandemic158. However, the relevance of these trials has been called into question now that COVID-19-specific vaccinations are available. Published efficacy data from the BioNTech/Pfizer159 and Moderna160 trials indicate vaccine efficacy rates of approximately 95%, with a third vaccine from The University of Oxford/AstraZeneca providing at least 62% protection161. Following the launch of national COVID-19 vaccination programmes in several countries, the question of whether such BCG trials ought to continue should be considered. Several important arguments have been made in support of continuing these trials162. First, the duration of protection conferred by COVID-19 vaccines and the extent to which the vaccine response is affected by co-morbidities and frailty in the elderly is unknown. One possibility is that a combination of BCG with a COVID-19-specific vaccine might aid the immune response and induce lasting protection. Furthermore, global demand for COVID-19 vaccines is likely to vastly outstrip available supply, with the vaccine remaining inaccessible to almost one-quarter of the world’s population until 2022 (ref.163). By contrast, BCG vaccines are widely available and might be useful to bridge the gap until production of COVID-19 vaccines is able to meet demand. Finally, establishing whether BCG vaccination is able to protect against COVID-19 severity might provide a tool for use against emerging pathogens in future pandemics.
The outlook for BCG vaccination for COVID-19
Until results from these trials are published, BCG vaccination should only be used for COVID-19 in a trial setting, according to the WHO guidance164; the BCG vaccine is already in short supply and use outside this setting risks jeopardizing supplies for TB prevention in endemic areas.
If trials demonstrate a positive treatment effect, a major concern for urologists f141and their patients will be how the supply of BCG for bladder cancer is affected. Urologists have faced global shortages of BCG for a decade and, in the short term, this shortage could be further exacerbated if BCG is repurposed for the COVID-19 effort. However, notably, the dose of BCG used for vaccination is 1/500th the dose used for bladder cancer treatment, meaning that, in theory, at least 500 subjects could be vaccinated from a single vial of BCG165. Furthermore, the renewed interest in BCG might encourage manufacturers who have hitherto been reluctant to increase production (or indeed, have left the market28) to become newly incentivized to increase BCG production, benefitting patients with bladder cancer and also increasing available vaccine supplies for TB prevention in endemic areas.
A century after the first use of BCG in humans, the vaccine has become established for the prevention of disseminated forms of TB and is also used intravesically as the standard treatment for high-risk NMIBC. Besides its use in TB and bladder cancer, the BCG vaccine might have beneficial non-specific effects and the mechanisms involved in such effects are now becoming better understood. Phase IV trials are currently underway to prospectively measure the role of these non-specific effects on protection against SARS-CoV-2 infection. Nevertheless, many questions regarding the mechanism of action of BCG remain, and it is hoped that these trials might provide new insights to improve our understanding of how to modulate the host response to prevent damage whilst protecting against infections, including COVID-19.
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S.B. declares that he has acted as a consultant for Ferring, Sanofi, ArTara and FerGene. P.C.B. declares that he is an advisory board member or equivalent for AbbVie, Asieris, AstraZeneca, Astellas, Bayer, Biosyent, BMS, EMD-Serono, Ferring, Fergene, H3-Biomedicine, Janssen, Merck, Roche, Sanofi, Urogen. He has received grant support or honoraria from iProgen, Sanofi, Bayer and GSK. P.C.B also holds a patent with Decipher Biosciences. J.J.M. declares that he acts as a consultant for Merck, AstraZeneca, Ferring, Cold Genesys, Janssen, Nucleix and Foundation Medicine. He has received research funding from AbbVie, Tesaro and Epizyme. D.M. declares that he has received grant support from AstraZeneca, Rainer Pharmaceuticals and honoraria from Janssen, Rainier Pharmaceuticals and H3 biomedicine. T.J.B. declares that he has acted as a consultant for FerGene, Genesis Biotechnology and Photocure. G.D.S declares that he is a member of clinical trial protocol committees for Merck, BMS, Janssen, Cold Genesys, Pfizer, PhotoCure and Fidia. He is or has been a scientific advisor/consultant within the past 5 years for Heat Biologics, Cold Genesys, PhotoCure, Merck, Roche/Genentech, Ciclomed, Taris Biomedical, MDxHealth, Fidia Farmaceuticals, Urogen, Ferring, Aduro, Boston Scientific, Bristol Myers Squibb, AstraZeneca, Pfizer, Janssen, Epivax Oncology, Natera, FKD, Ferring, EnGene Bio, SesenBio, BioCanCell, Nucleix, Ipsen, Combat Medical, Astellas, Fergene, Dendreon, AbbVie and Seattle Genetics. A.M.K. is a consultant or advisory board member for Abbott Molecular, Arquer Diagnostics, ArTara Therapeutics, Asieris Pharmaceuticals, AstraZeneca, BioClin Therapeutics, Bristol Myers Squibb, Cepheid, Cold Genesys, Eisai, Engene, Ferring Pharmaceuticals, FerGene, Imagine Pharma, Janssen, MDxHealth, Medac, Merck, Pfizer, Photocure, ProTara Therapeutics, Roviant Sciences, Seattle Genetics, Sessen Bio, Theralase Technologies, TMC Innovation and US Biotest. A.M.K. has received grants and/or research support from Adolor Corporation, Bristol Myers Squibb, FKD Industries, Heat Biologics, Merck, Photocure, SWOG/NIH, Specialized Programs of Research Excellence (SPORE) and AIBCCR. A.M.K. also holds the patent for Cytokine Predictors of Response to Intravesical Therapy (CyPRIT) joint with UT MD Anderson Cancer Center. The other authors declare no competing interests.
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Lobo, N., Brooks, N.A., Zlotta, A.R. et al. 100 years of Bacillus Calmette–Guérin immunotherapy: from cattle to COVID-19. Nat Rev Urol 18, 611–622 (2021). https://doi.org/10.1038/s41585-021-00481-1
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