Abstract

Bacillus Calmette–Guerin (BCG) is a live attenuated form of Mycobacterium bovis that was developed 100 years ago as a vaccine against tuberculosis (TB) and has been used ever since to vaccinate children globally. It has also been used as the first-line treatment in patients with nonmuscle invasive bladder cancer (NMIBC), through repeated intravesical applications. Numerous studies have shown that BCG induces off-target immune effects in various pathologies. Accumulating data argue for the critical role of the immune system in the course of neurodegenerative diseases such as Alzheimer’s disease (AD) and Parkinson’s disease (PD). In this study, we tested whether repeated exposure to BCG during the treatment of NMIBC is associated with the risk of developing AD and PD. We presented a multi-center retrospective cohort study with patient data collected between 2000 and 2019 that included 12,185 bladder cancer (BC) patients, of which 2301 BCG-treated patients met all inclusion criteria, with a follow-up of 3.5 to 7 years. We considered the diagnosis date of AD and nonvascular dementia cases for BC patients. The BC patients were partitioned into those who underwent a transurethral resection of the bladder tumor followed by BCG therapy, and a disjoint group that had not received such treatment. By applying Cox proportional hazards (PH) regression and competing for risk analyses, we found that BCG treatment was associated with a significantly reduced risk of developing AD, especially in the population aged 75 years or older. The older population (≥75 years, 1578 BCG treated, and 5147 controls) showed a hazard ratio (HR) of 0.726 (95% CI: 0.529–0.996; p-value = 0.0473). While in a hospital-based cohort, BCG treatment resulted in an HR of 0.416 (95% CI: 0.203–0.853; p-value = 0.017), indicating a 58% lower risk of developing AD. The risk of developing PD showed the same trend with a 28% reduction in BCG-treated patients, while no BCG beneficial effect was observed for other age-related events such as Type 2 diabetes (T2D) and stroke. We attributed BCG’s beneficial effect on neurodegenerative diseases to a possible activation of long-term nonspecific immune effects. We proposed a prospective study in elderly people for testing intradermic BCG inoculation as a potential protective agent against AD and PD.

Highlights

  • Bacillus Calmette–Guérin (BCG), a live attenuated form of Mycobacterium bovis, was developed 100 years ago as a vaccine against tuberculosis (TB) [1]

  • We proposed the evaluation of the association between BCG treatment and the risk of developing Alzheimer’s disease (AD) and Parkinson’s disease (PD) in three retrospective cohorts from Israel and California by comparing bladder cancer (BC) patients treated with BCG instillations following transurethral resection of bladder tumor (TURBT), with BC patients not treated with BCG

  • The mean follow-up time in the CHS cohort was similar between the BCG and BCG-free groups (2640 (±1360) vs. 2610 (±1540)), whereas the mean followup time in the Hadassah University Hospitals (HUH) cohort was significantly longer for the BCG group (2870 (±1840) vs

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Summary

Introduction

Bacillus Calmette–Guérin (BCG), a live attenuated form of Mycobacterium bovis, was developed 100 years ago as a vaccine against tuberculosis (TB) [1]. BCG is administered intradermally at birth and has been shown to protect against TB, with an effect that lasts between 15 and 20 years [2,3]. Following BCG vaccination, changes in the epigenetic signature, transcription, and hematopoietic cell function [4] are evident. These alterations reflect the BCG-induced trained innate immunity [5,6]. BCG induces the expansion of antigen-presenting cells of the adaptive immune response (e.g., dendritic and T-cells) [5,9] Changes in bone marrow-derived hematopoietic stem and progenitor cells (BM-HSPCs) and monocytes lead to an increase in cytokine secretion (e.g., IL-1β, TNFα, MCP-1, and IL-8) [7], and the activation of lymphocytes, monocytes, neutrophils [8], and natural killer (NK) cells [6].

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