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These compounds are often classified as nutraceuticals or dietary supplements, which are not subject to the same rigorous testing and regulatory requirements as pharmaceutical drugs.200 However, for senomorphic therapies to be used as effective interventions, they will likely need to undergo extensive clinical testing and receive approval from health authorities like the FDA or EMA.126 Regulatory frameworks may need to be adapted to accommodate new therapeutic paradigms based on modulating senescence

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The extent to which ADE contributes to COVID-19 immunopathology is being actively investigated

Autoimmune disease-related hub genes are potential biomarkers and associated with immune microenvironment in endometriosis