• interferon inducers
• urinary bladder neoplasms
• immunotherapy
• B-lymphocytes
• adjuvants, immunologic

The observation that microbes could curb cancer growth was made over 4000 years ago when incisions on tumors led to infection mediated spontaneous regression. In modern medicine, the therapeutic potential of microbes, or their components, against cancer was first demonstrated by William Coley in 1891. Although Coley’s toxins did not come into wide clinical practice due to inconsistencies in the type of cancers treated, routes of administration and variable outcomes from this clinical experience established the proof-of-concept that stimulating the immune system using microbes or their components can be an adjunctive treatment to surgery and cytotoxic therapy. Although this was followed by sporadic successes in other solid tumors, a major success pioneering the field of cancer immunotherapy was introduction of intravesical administration of BCG for the treatment of non-muscle invasive bladder cancer (NMIBC).1 This was one of the very few initial testaments of benefits from weakened or modified microbes and their specific molecular patterns for antitumor immune sensitization. Despite ongoing global shortages, BCG immunotherapy remains the gold-standard treatment for NMIBC. Over the last 100 years, BCG vaccine has been the only tuberculosis (TB) preventative strategy and is quite eloquently described as ‘the vaccine that keeps on giving’.2 Infant/childhood BCG vaccination via intradermal administration continues to be practiced in several countries to prevent TB.2 An intriguing association between BCG vaccination and incidence from the ongoing COVID-19 is a recent stirring although a controversial observation. Countries with national vaccination programs (eg, India, Korea, Japan) for TB prevention, using BCG vaccine, showed a much lower morbidity and mortality from severe COVID-19 compared with those (eg, Italy, USA, UK) that do not have such policies.3 Although this observation was not confirmed by others,4 an immediate response to this ecological finding was initiation of COVID-19 clinical trials evaluating BCG (https://clinicaltrials.gov/ct2/results?cond=BCG+and+COVID-19) and its recombinant form VPM1002 (https://clinicaltrials.gov/NCT04387409), to protect healthcare workers and the elderly.

BCG remains as one of the best-known vaccines associated with beneficial and heterologous protection from other diseases. The ‘pathogen agnostic’ effects of BCG span from reducing sepsis associated mortality,2 protection against other forms of TB, potentiating antiviral (Respiratory syncitial virus, yellow fever caused by an RNA virus) immune responses and most importantly reducing cancer recurrence and progression.5 This non-specific effect of BCG is described to be at least partially mediated via innate immune memory/trained immunity through microbe-induced epigenetic changes in cells of the innate and adaptive immune systems.5 While trial outcomes from BCG vaccination induced protection of healthcare workers from COVID-19 are awaited to further support this interesting and promising association, several questions arise: (1) Is this protective effect age- and sex-dependent? (2) How long does the protection last? (3) Can BCG synergize with currently approved immunomodulatory agents? (4) Given the variability in immune cell composition across tissues, is the effect location/tissue type dependent? (5) Does the dose, route, duration, number and frequency of administration weigh on the effect? (6) Does the host genetics influence response? (7) Will the strain of BCG vaccine induce a variable response? (8) Will lung associated comorbidities cause a deleterious effect due to a chronic inflammatory state and most importantly (9) How could these investigations impact NMIBC treatment?

While revisiting the parallels of antiviral and anticancer immunity, interferons (IFN) undoubtedly lie at a major intersection between these two pathologies. Viral infection antagonizes cytosolic innate sensing pathways such as the Retinoic acid-inducible gene (RIG-1) and cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS)-STimulator of INterferon Genes (STING) pathways to evade protective IFN response. Mimicking such viral immune evasion mechanisms, cancer cells often adapt to an impaired IFN-1 signaling and thus modulate the associated microenvironment toward a suppressive phenotype conducive to their growth and metastasis. Both type I and II IFN (IFN-α/β and IFN-γ, respectively) are critical to these effects and, therefore, effort has focused on their direct or indirect activation via vaccination and/or therapeutic introduction in order to induce or magnify a protective IFN response.

This brings us to the question; How does BCG impart its non-specific protective effect against viral infections or its anticancer effect and are they IFN dependent? Studies from Netea and colleagues have extensively investigated and explained this concept and role of innate immune memory within macrophages.5 Yao et al further demonstrated that at mucosal sites, CD8⁺ T cell help was indispensable for priming of such memory within the lung resident alveolar macrophages.6 Subsequent downstream effects extrinsic to macrophages, such as chemokine mediated immune cell recruitment to the site of infection/inflammation, further activation of the adaptive immune responses and the influence of tissue specific immune microenvironment are some key factors to the overall favorable outcomes that depend on the initial magnitude of macrophage priming. In our effort to further gain a deeper understanding of BCG induced protective effects and enhance them, we must consider the unique pathogenesis of Mycobacterial infection and host responses towards controlling its spread. One such unique feature that is seen across the spectrum of various TB states, is granuloma formation.7 Granuloma formation is considered to be a hallmark of Mycobacterial infection. Mycobacterium tuberculosis (MTB) induced granuloma and is constituted by an aggregate of macrophages and lymphocytes and develops as a result of host immune responses to contain the bacterial spread. Interestingly, TB associated/pathogenic Mycobacteria-induced protective, chronic granuloma also exhibits remarkable similarities to an ectopic/tertiary lymphoid structure (TLS), a predominant feature of mucosa associated lymphoid tissue containing innate and adaptive immune cells with similar architecture as seen in a canonical germinal center in secondary lymphoid organs.7 Indeed, IFN-1 signaling and downstream immune cell chemotaxis to the site of infection, are central to the formation of these TLSs and maturation of B cells including antibody class switching and affinity maturation within these.8

Following birth, TLSs develop at mucosal sites (eg, respiratory, gut and urogenital tract). TLSs also form as a result of exposure to normal commensal and pathogenic microbes and chronic inflammation (eg, chronic obstructive pulmonary disease; COPD and cancer) and generally provide heterologous humoral immune protection.8 Higher frequency of these TLSs, also known as induced bronchus associated lymphoid tissues (iBALTs) in the respiratory mucosa, is protective against respiratory infections such as Influenza A virus, severe acute respiratory syndrome coronavirus (SARS-CoV) and MTB.8 The proximity of vaccine-induced iBALTs to respiratory pathogens leads to rapid B-cell maturation, antibody production and T cell priming. Mucosal delivery of BCG (either lung or bladder) also leads to delayed granuloma/iBALT formation as well as B cell activation, reminiscent of pathogenic Mycobacteria-associated granuloma. In contrast, pathogenic iBALTs also develop in autoimmune diseases and in respiratory pathologies such as asthma, smoking, hypertension, COPD. Irrespective of the initial insult/challenge, IFN-1 is critical to TLS organogenesis.8

Similar to mucosal vaccination associated granuloma formation, in the case of NMIBC, BCG delivered into the bladder lumen/mucosa also leads to granuloma formation.9 10 To compensate for lack of response to BCG given its inability to induce IFN-1 activation, exogenously delivered recombinant IFN-α has been extensively evaluated in this cancer.10 Adenoviral vector expressing IFN-α2b is also currently in phase III trials (https://clinicaltrials.gov/NCT02773849). Over the past few years, several studies have been conducted to identify factors underlying reduced efficacy of BCG to activate an IFN-1 response.

BCG is derived via attenuation of Mycobacterium bovis. The loss of early secretory antigenic target secretion system-1 (ESX-1), one of the immunodominant antigens, as a result of attenuation for vaccine preparation, impairs the ability of BCG to activate the cGAS-STING/IRF3, RIG/MAVS/IRF7 cytosolic nucleic acid sensing pathways.11 As such, there is minimal IFN-β production, while some protection is imparted through cytokine induction and downstream immunological effects via NLRP3 inflammasome activation within macrophages, dendritic cells and epithelial cells.11 To compensate for this IFN-1 activation defect, several recombinant versions of BCG have been generated. VPM1002 is a promising recombinant BCG that activates the AIM2 inflammasome and the STING pathway and has also been demonstrated to impart significantly higher protection over conventional BCG in phase I and II trials.12 Indeed, VPM1002 is also being trialed in healthcare workers and the elderly to protect against severe COVID-19 . While the outcomes of these trials are awaited, based on previous studies, it is relevant and timely to hypothesize that mucosal delivery of BCG combined with a STING pathway activator as an adjuvant may lead to the desired neogenesis of iBALTs in the respiratory mucosa that may offer enhanced or better protection against COVID-19 (figure 1). Most importantly, as the positive impact of B cells in antitumor immunity is being recognized, specifically those that are associated with TLSs formed post immune checkpoint blockade therapy in sarcoma, melanoma and lung cancer, further research is warranted towards their therapeutic induction across cancers.13 Heterologous protection similar to BCG-induced trained immunity has also been reported with respect to measles and polio vaccines.14 15 Given the critical role of dendritic cells in TLSs and their potent IFN-1 producing characteristic, microbe-based therapeutics, such as oncolytic viruses could also investigate similar immune memory associated effects to increase durable antitumor immune response.

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Figure 1

Hypothetical diagram showing enhanced protection by intranasally delivered BCG (in combination with a sting pathway activator) or with recombinant BCG (VPM1002), against SARS-CoV2 viral infection. iBALT, induced bronchus associated lymphoid tissue; STING, STimulator of INterferon Genes; TLS, tertiary lymphoid structure; DC, Dendritic cell; SARS-CoV2, Severe acute respiratory syndrome-coronavirus 2.

The wide spectrum of protection using BCG vaccine against non-related pathogens and cancer to enhance innate immunity and bridge adaptive immune responses, emphasizes the urgent need to revisit such microbe-based combination therapeutics for cancer treatment, specifically via local administration. Unfortunately, the ongoing global shortage of BCG has affected routine management of patients with bladder cancer in addition to compromising infant vaccination in some countries. The lessons learned from BCG-induced non-specific protection across infectious and non-infectious diseases could be adapted toward development of similar microbe-based therapies such as oncolytic viruses, Bifidobacteria and others that activate IFN-1 via the STING pathway and potentially mediate innate immune sensitization for immune checkpoint blockade via induction of TLS formation.