Could the gut be involved in the development of multiple sclerosis?

Could the gut be involved in the development of multiple sclerosis?
iStock-Pornpak Khunatorn

The gut has long been suspected to play a role in autoimmune disease; a research team has now identified evidence of a potential mechanism.

Currently, it is incompletely understood which factors in patients with multiple sclerosis (MS) act as a trigger for the immune system to attack the brain and spinal cord. The new research has now made a link between the gut and the development of multiple sclerosis.

A potential factor is described by a research team in the journal Proceedings of the National Academy of Sciences.

The medical researchers used an animal model to show that the protein Smad7 mobilises immune cells in the intestines which, in turn, trigger inflammation in the central nervous system.

Analyses of intestinal tissue samples taken from MS patients confirmed the results.

The study was conducted at the Department of Neurology and the Centre of Neuroimmunology at St. Josef-Hospital, university hospital of Ruhr-Universität Bochum.

Activating immune cells in the intestines

The research team initially analysed the signal protein Smad7 in intestinal immune cells in mice, or more precisely: in T-cells.

The researchers compared genetically modified mice with a normal and those with a particularly high quantity of Smad7 in T-cells as well as mice without any Smad7 in T-cells. They monitored if the animals developed opticospinal encephalomyelitis – a disease that mimics MS in humans.

The strongest clinical MS-like symptoms occurred in animals with an increased Smad7 level in T-cells.

In their intestines, T-cells were more frequently activated, which then migrated into the central nervous system where they triggered inflammation. Moreover, the ratio of protective regulatory T-cells to pathogenic autoreactive T-cells had changed. In mice that didn’t have any Smad7 protein, no clinical signs of a MS-like disease occurred.

Results confirmed using tissue samples from patients

In the next step, the researchers analysed tissue samples taken from the intestines of 27 MS patients and compared them with samples taken from 27 healthy individuals. In the patients, they identified changes similar to those in the animal model.

The signal protein Smad7 occurred more frequently in intestinal mucosa samples of MS patients than in those of healthy individuals; in addition, an abnormal ratio of regulatory to pathogenic mechanisms was identified in intestinal mucosa samples in patients.

Neurologist on the study, Professor Ingo Kleiter, at Marianne-Strauß-Klinik in Berg, said: “For other autoimmune diseases such as Crohn’s and other inflammatory bowel diseases, researchers are already aware that Smad7 offers a promising therapeutic target; our results suggest that the same is true for multiple sclerosis.”.

“Researchers are increasingly exploring intestinal involvement in the progression and development of multiple sclerosis,” adds Simon Faissner.

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