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Updated: Oct 16, 2025

Therapeutic Evaluation of Fecal Microbiota Transplantation in an Interleukin 10-Deficient Mouse Model
Published on: April 6, 2022
Primary immunodeficiency and the microbiome
Maryam Ali Al-Nesf1,2, David Morgan3, Vidya Mohamed-Ali4,2
1Allergy and Immunology Section, Hamad Medical Corporation, Doha, Qatar.
Purpose Of Review:
The current understanding of the relationship of the microbiota to clinical manifestation in patients with primary immunodeficiency, specifically the inflammatory processes caused by or that result in microbial dysbiosis, and their potential therapeutic options in primary immunodeficiency diseases (PID), is the basis of this review.
Recent Findings:
PIDs are heterogeneous diseases with variable presentations, genetic backgrounds, complications, and severity. The immune-mediators may be extrinsic, such as therapeutic regimens that patients are on, including immunoglobin, biologics, antibiotics and diet, or intrinsic, like cytokines, microRNA and microbiome. The microbiome in PID, in particular, appears to play a crucial role in helping the host's immune system maintain hemostatic control in the intestine. Many of the clinical manifestations and complications of PID may be attributed to inflammatory and immune dysregulatory processes connected to the imbalances of the diet-microbiota-host-immunity axis, as shown by data pointing to the loss of microbial diversity, dysbiosis, in PID.
Summary:
The gut microbiome is a promising area of study in PID. Although the connection of the microbiome to humoral immunodeficiency is evident, the possibility of utilizing the association of humoral and cellular immunodeficiency and the microbiome for therapeutic benefit is still under investigation.
Insights
Microbial dysbiosis, an imbalance in gut bacteria, is linked to inflammation and complications in primary immunodeficiency diseases (PID). Research is exploring microbiome-targeted therapies for PID, offering potential new treatment avenues.
Area of Science:
- Immunology
- Microbiology
- Gastroenterology
Background:
- Primary immunodeficiency diseases (PIDs) are a diverse group of genetic disorders affecting the immune system.
- The gut microbiome plays a critical role in maintaining host immune homeostasis, particularly in the intestine.
- Imbalances in the diet-microbiota-host-immunity axis, characterized by loss of microbial diversity and dysbiosis, are implicated in PID manifestations.
Purpose of the Study:
- To review the current understanding of the relationship between the microbiota and clinical manifestations in patients with primary immunodeficiency.
- To explore the role of microbial dysbiosis in inflammatory processes within PID.
- To discuss potential therapeutic strategies targeting the microbiome in PID.
Main Methods:
- Literature review of studies on the gut microbiome in primary immunodeficiency diseases.
- Analysis of the impact of microbial dysbiosis on immune dysregulation and inflammation in PID.
- Synthesis of current research on therapeutic interventions related to the microbiome in PID.
Main Results:
- Data suggests that alterations in microbial diversity and dysbiosis are associated with clinical manifestations and complications in PID.
- The microbiome appears crucial for maintaining intestinal immune control, and its imbalance contributes to inflammatory processes.
- While the link between the microbiome and humoral immunodeficiency is recognized, its therapeutic potential in PID is an active area of investigation.
Conclusions:
- The gut microbiome is a significant factor in the pathogenesis and clinical presentation of PID.
- Understanding the interplay between the microbiome and the immune system in PID opens avenues for novel therapeutic approaches.
- Further research is needed to fully elucidate and harness the therapeutic potential of microbiome modulation in PID, especially for combined humoral and cellular immunodeficiencies.
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