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Multiple indirect cellular and microbiome mediators

Molecular classification
Other
01

Overview

The designation Multiple indirect cellular and microbiome mediators refers to a therapeutic paradigm where the clinical efficacy is derived from systemic or ecological changes rather than binding to a specific human protein target. This is particularly relevant for microbiome-directed therapies, where the target is the collective genome and metabolic activity of trillions of microorganisms (Cani, P. D., 2018, Gut). Interventions such as fecal microbiota transplants or certain non-absorbed antibiotics work by reshaping the microbial landscape, which in turn alters the profile of signaling metabolites like short-chain fatty acids and bile acids (Surawicz et al., 2013, American Journal of Gastroenterology). These metabolites interact with various host receptors to modulate inflammation, glucose homeostasis, and gut barrier function (Forslund et al., 2015, Nature). Consequently, this category encompasses treatments for diverse conditions ranging from enteric infections to metabolic and autoimmune diseases. Because the mechanism involves a complex network of indirect interactions, identifying a single molecular target is often impossible or biologically inaccurate.

Other names
Microbiome-mediated pathwaysIndirect cellular mediatorsNon-specific microbial modulationCommensal microbiota modulation
02

Mechanism of action

Modulation of the gut microbiota composition and the subsequent production of bioactive metabolites (e.g., short-chain fatty acids, bile acids) that influence host physiological pathways (Nature Reviews Microbiology, 2013).

03

Biological functions

Microbiome modulationImmune response regulationMetabolic homeostasisGut barrier maintenance
04

Disease associations

InfectionInflammationMetabolic diseaseGastrointestinal disorders
05

Safety considerations

Risk of systemic infection in immunocompromised patientsUnintended shifts in microbial ecology (dysbiosis)High inter-individual variability in therapeutic responsePotential for transfer of antibiotic resistance genes
06

Interacting drugs

Rifaximin

4 more in the full profile.

07

Biomarkers

Microbial alpha-diversity indexFecal calprotectinShort-chain fatty acid (SCFA) concentrationSecondary bile acid levels

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