US researchers have identified a mechanism that causes severe gastrointestinal problems with immune-based cancer treatment.
The team from the University of Michigan Health Rogel Cancer Center also found a way to deliver immunotherapy’s cancer-killing impact without the unwelcome side effect.
The findings are published in Science.
“This is a good example of how understanding a mechanism helps you to develop an alternative therapy that’s more beneficial. Once we identified the mechanism causing the colitis, we could then develop ways to overcome this problem and prevent colitis while preserving the anti-tumor effect,” said Gabriel Nunez, Professor of Pathology at Michigan Medicine.
Immunotherapy has emerged as a promising treatment for several types of cancer.
But immune checkpoint inhibitors can also cause severe side effects, including colitis, which is inflammation in the digestive tract.
Colitis can cause severe gastrointestinal discomfort, and some patients will discontinue their cancer treatment because of it.
The problem facing researchers was that while patients were developing colitis, the laboratory mice were not. So researchers couldn’t study what was causing this side effect.
For the study, the team created a new mouse model, injecting microbiota from wild-caught mice into the traditional mouse model.
In this model, the mice did develop colitis after administration of antibodies used for tumor immunotherapy.
Now, researchers could trace back the mechanism to see what was causing this reaction.
In fact, colitis developed because of the composition of the gut microbiota, which caused immune T cells to be hyper-activated while regulatory T cells that put the brakes on T cell activation were deleted in the gut.
This was happening within a specific domain of the immune checkpoint antibodies.
Researchers then removed that domain, which they found still resulted in a strong anti-tumor response but without inducing colitis.
“Previously, there were some data that suggested the presence of certain bacteria correlated with response to therapy. But it was not proven that microbiota were critical to develop colitis. This work for the first time shows that microbiota are essential to develop colitis from immune checkpoint inhibition,” Nunez said.
To follow up what they saw in mice, researchers reanalysed previously reported data from studies of human cells from patients treated with immune checkpoint antibodies, which reinforced the role of regulatory T cells in inducing colitis.
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