Combining discoveries in cancer immunology with sophisticated genetic engineering, Columbia University researchers have created a sort of “bacterial suicide squad” that targets tumours, attracting the host’s own immune cells to the cancer to destroy it.
The new work, published today in Science Advances, marks a major step forward in efforts to enlist non-pathogenic bacteria to combat cancer.
Scientists have known for years that some species of bacteria can thrive inside tumours.
“It’s been speculated that this is due to the low pH, necrotic and immune-excluded environment … that’s unique to the core of a tumour and supports bacterial growth while preventing clearance of bacteria by immune cells,” says Nicholas Arpaia, PhD, assistant professor of microbiology and immunology at Columbia’s Vagelos College of Physicians and Surgeons and senior author on the new paper.
In an ongoing collaboration with Tal Danino, PhD, associate professor of biomedical engineering at Columbia Engineering, Dr Arpaia has been building an anti-tumour strategy around that phenomenon.
At the core of the approach is a probiotic strain of the bacterium E coli, engineered with a synchronised lysis circuit.
Once the bacterial cells reach a quorum inside a tumour, the circuit triggers, causing most of the bacteria to lyse, or break apart, releasing their contents.
Previously, the investigators have added genes to the microbes encoding proteins that block tumour cell growth, or that flag the tumour for digestion by immune cells.
“My graduate student, Thomas [Savage], had the idea of potentially utilising this platform to deliver chemokines,” says Dr Arpaia, who is also a member of the Herbert Irving Comprehensive Cancer Center (HICCC) at NewYork-Presbyterian/Columbia University Irving Medical Center.
Immunologists have found that different chemokines, immune system inhaling proteins, attract different types of immune cells and stimulate them to respond in specific ways.
In the new work, the team included a mutated version of a human chemokine gene that attracts “killer” T cells.
“Although T cell responses that are specific to tumour-derived antigens are primed, sometimes what will happen is that despite there being primed anti-tumour T cells, they fail to be recruited into the tumour environment,” says Dr Arpaia.
To further augment therapeutic efficacy, the researchers added a second bacterial strain expressing another chemokine, this time to attract dendritic cells.
“By coupling this with chemokines that drive the infiltration and activation of dendritic cells, a critical innate immune cell type, detection of tumour antigens is increased,” says Dr Arpaia.
Activated dendritic cells eat the tumour cells, then present their antigens to the T cells, which can then recognise the tumour cells better and respond to them more reliably.
The new work involved collaborators from the Department of Pathology and Cell Biology, the HICCC and the Data Science Institute at Columbia, and also built on a long series of previous findings by others.
“Through decades of research that’s allowed us to understand how an immune response develops, [we’re] developing therapeutics that specifically target each one of those discrete steps,” says Dr Arpaia.
In mouse models of cancer, the engineered bacteria induce robust immune responses against tumours that have been injected directly with the bacteria, as well as more distant tumours that weren’t injected.
Delivering the bacteria intravenously also works.
“What we see is that the bacteria will only colonise the tumour environment, and they only reach a sufficient level of quorum to induce lysis within the tumour, so we can’t detect bacteria in other healthy organs,” says Dr Arpaia.
The scientists continue to tinker with the system to optimise it, while also laying the groundwork to take it into clinical trials.
Dr Arpaia and some of his collaborators have applied for a patent on the approach.
Source: Columbia University
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