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Published on: September 22, 2019
Intestinal Microbiota in Common Chronic Inflammatory Disorders Affecting Children
Anna Torun1, Anna Hupalowska2, Piotr Trzonkowski3
1Chair and Department of Biochemistry, Medical University of Warsaw, Warsaw, Poland.
Insights
Pediatric chronic inflammatory disorders are linked to gut microbiome changes. New immunotherapies, enhanced by gut microbiota modulation, show promise for treating conditions like inflammatory bowel disease and autoimmune diseases.
Area of Science:
- Pediatric immunology and gastroenterology.
- Microbiome research and immune system interactions.
Background:
- Rising incidence of pediatric chronic inflammatory disorders.
- Gut microbiome alterations implicated in inflammatory bowel disease (IBD), type 1 diabetes mellitus (T1DM), and celiac disease (CeD).
- Current therapies offer symptomatic relief but lack sustained improvements.
Purpose of the Study:
- Review pathogenic mechanisms of pediatric chronic inflammatory disorders.
- Summarize the role of gut microbiota disturbances.
- Explore novel therapeutic strategies targeting the microbiome and immune system.
Main Methods:
- Review of recent preclinical studies and clinical trials.
- Analysis of pathogenic mechanisms and microbiota composition.
- Evaluation of immunotherapies and microbiota modulation.
Main Results:
- Gut microbiota composition and abundance are key factors in IBD, T1DM, and CeD development.
- New approaches like engineered T cells show therapeutic potential.
- Microbiota manipulation can enhance immunotherapy responses.
Conclusions:
- Targeting the gut microbiome and immune system offers promising avenues for pediatric chronic inflammatory disorders.
- Restoring gut microbiota balance is crucial for long-term health benefits.
- Integrated therapeutic strategies hold potential for improved quality of life in affected children.
Abstract:
The incidence and prevalence rate of chronic inflammatory disorders is on the rise in the pediatric population. Recent research indicates the crucial role of interactions between the altered intestinal microbiome and the immune system in the pathogenesis of several chronic inflammatory disorders in children, such as inflammatory bowel disease (IBD) and autoimmune diseases, such as type 1 diabetes mellitus (T1DM) and celiac disease (CeD). Here, we review recent knowledge concerning the pathogenic mechanisms underlying these disorders, and summarize the facts suggesting that the initiation and progression of IBD, T1DM, and CeD can be partially attributed to disturbances in the patterns of composition and abundance of the gut microbiota. The standard available therapies for chronic inflammatory disorders in children largely aim to treat symptoms. Although constant efforts are being made to maximize the quality of life for children in the long-term, sustained improvements are still difficult to achieve. Additional challenges are the changing physiology associated with growth and development of children, a population that is particularly susceptible to medication-related adverse effects. In this review, we explore new promising therapeutic approaches aimed at modulation of either gut microbiota or the activity of the immune system to induce a long-lasting remission of chronic inflammatory disorders. Recent preclinical studies and clinical trials have evaluated new approaches, for instance the adoptive transfer of immune cells, with genetically engineered regulatory T cells expressing antigen-specific chimeric antigen receptors. These approaches have revolutionized cancer treatments and have the potential for the protection of high-risk children from developing autoimmune diseases and effective management of inflammatory disorders. The review also focuses on the findings of studies that indicate that the responses to a variety of immunotherapies can be enhanced by strategic manipulation of gut microbiota, thus emphasizing on the importance of proper interaction between the gut microbiota and immune system for sustained health benefits and improvement of the quality of life of pediatric patients.
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