This work provides an integrated theoretical and translational roadmap for next‐generation disease‐modifying OA therapies, focusing on how renewable biomaterials, engineered exosomes, and their composite systems target and regulate the pathological network to restore joint homeostasis.
Abstract
Osteoarthritis (OA) is a prevalent, chronic degenerative joint disease characterized by progressive cartilage degeneration and impaired joint function. Its rising global incidence poses a significant health and socioeconomic burden. Traditional therapies primarily offer symptomatic relief but fail to halt disease progression and are associated with notable limitations. The contemporary understanding of OA pathogenesis has evolved from a model of mechanical wear to one emphasizing systemic imbalance within the joint microenvironment, involving immune dysregulation, metabolic disturbances, cellular senescence, and the gut‐joint axis. This paradigm shift supports the development of innovative, disease‐modifying strategies. This review is structured around a unifying multi‐axis microenvironmental imbalance model for osteoarthritis. It systematically integrates the crosstalk and cascade‐amplifying mechanisms of immune dysregulation, cellular senescence, metabolic disturbances, and the gut–joint axis, clarifying that multi‐dimensional microenvironmental disruption collectively forms the pathological core of OA. We focus on how renewable biomaterials, engineered exosomes, and their composite systems target and regulate the pathological network to restore joint homeostasis, enabling a paradigm shift from symptomatic management to root‐cause intervention. This work provides an integrated theoretical and translational roadmap for next‐generation disease‐modifying OA therapies.
The bidirectional crosstalk between immune and metabolic processes during OA progression is summarized and integrating multi-omics technologies with personalized medicine may improve patient stratification and dynamic monitoring and could facilitate the future development of more personalized and potentially disease-mo...
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Biologic and regenerative interventions represent promising avenues for advancing cartilage repair and improving clinical outcomes in patients with osteoarthritis, and current evidence indicates that these therapies exert their effects through modulation of inflammatory pathways, enhancement of extracellular matrix syn...
Hai-Yuan Yue, Ahmad Alhaskawi, S. Ezzi et al.· Frontiers in Pharmacology· 0 citations
Osteoarthritis (OA) has conventionally been considered a degenerative mechanical condition; but an increasing number of studies support an alternative perception of this disease as one characterized by impaired immune homeostasis in the joint environment. The purpose of this review is to analyze the mechanisms of how t...
Bone aging is not merely a process of bone mass loss but rather a multi-level, networked degenerative phenomenon spanning molecular, cellular, tissue, and system levels. With the accelerating pace of global population aging, bone degenerative diseases have emerged as a major public health challenge. Consequently, there...
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Osteoarthritis (OA) is a heterogeneous whole-joint disorder in which pain, structural progression and treatment response often diverge from radiographic severity. This mismatch has limited disease-modifying OA drug development and highlights the need for biologically informed patient stratification. Chronic low-grade i...
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Osteoarthritis (OA) is a whole-joint disease characterized by progressive structural degeneration and chronic low-grade inflammation affecting the cartilage, synovium, subchondral bone, and immune compartments. It is a complex degenerative disorder associated with substantial morbidity, heterogeneous clinical trajector...
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