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[The intestinal microbiota composition in patients with multiple sclerosis receiving different disease-modifying
I N Abdurasulova1, E A Tarasova2, I G Nikiforova3
1Institute of Experimental Medicine, St-Petersburg, Russia; St-Petersburg State Pediatric Medical University, St-Petersburg, Russia.
Aim:
To describe characteristics of the intestinal microbiota in patients with multiple sclerosis (MS) treated with glatiramer acetate (GA) or fingolimode (FG) for understanding causal relationships between gut microbiota and autoimmune processes in MS patients.
Material And Methods:
The study included 34 patients treated with GA (n=17) or FG (n=17). GA was used in a dose of 20 mg/kg subcutaneously once a day, FG in a dose of 0.5 mg daily. All patients were examined during remission. To assess the composition of gut microbiota, bacteriological and real-time PCR techniques were used. DNA was extracted from feces using DNA-EXPRESS kit.
Results And Conclusion:
There was a decrease in numbers of Escherichia coli with normal enzymatic activity, which was replaced by atypical forms of E. coli, Enterobacter spp. and fungi of the genus Candida, and, during treatment with GA, by atypical forms of E. coli, Proteus spp., Parvimonas micra. These differences indicate the effect of the therapy on the intestinal microbiota composition.
Insights
Multiple sclerosis (MS) therapies, glatiramer acetate (GA) and fingolimod (FG), alter gut microbiota composition. These treatments reduced beneficial bacteria, increasing opportunistic pathogens like E. coli and fungi.
Area of Science:
- Microbiology
- Immunology
- Neurology
Background:
- Multiple sclerosis (MS) is an autoimmune disease affecting the central nervous system.
- The gut microbiota plays a role in immune system regulation and may influence autoimmune processes.
- Understanding the impact of MS therapies on gut microbiota is crucial for developing targeted treatments.
Purpose of the Study:
- To characterize the intestinal microbiota in MS patients treated with glatiramer acetate (GA) or fingolimod (FG).
- To investigate potential causal relationships between gut microbiota alterations and autoimmune processes in MS.
- To assess the influence of specific MS immunomodulatory drugs on gut microbial composition.
Main Methods:
- Fecal samples were collected from 34 MS patients (17 on GA, 17 on FG) during remission.
- Bacteriological and real-time PCR techniques were employed to analyze gut microbiota composition.
- DNA extraction from fecal samples was performed using the DNA-EXPRESS kit.
Main Results:
- A decrease in Escherichia coli with normal enzymatic activity was observed.
- Atypical forms of E. coli, Enterobacter spp., and Candida spp. increased in patients.
- GA treatment was associated with atypical E. coli, Proteus spp., and Parvimonas micra.
Conclusions:
- Glatiramer acetate and fingolimod therapies significantly alter the intestinal microbiota composition in MS patients.
- These alterations include a reduction in specific beneficial bacteria and an increase in opportunistic pathogens.
- The observed changes suggest a link between MS immunomodulatory treatments and gut microbial dysbiosis.
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