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Multiple immune cell populations and inflammatory pathways refers to the integrated network of leukocytes—including T cells, B cells, myeloid cells, and innate lymphoid cells—and the intracellular signaling cascades that govern their activation and effector functions (Medzhitov, R., Nature, 2008). These pathways, such as the NF-κB, JAK-STAT, and Toll-like receptor (TLR) signaling routes, coordinate the production of cytokines and chemokines to mount a defense against pathogens (Taniguchi & Karin, Cell, 2018). In many chronic diseases, these systems become dysregulated, leading to persistent tissue damage and functional impairment (StatPearls, Inflammation, 2023). Therapeutic strategies targeting this broad system often utilize corticosteroids or multi-target immunosuppressants to dampen overactive immune responses (Journal of Allergy and Clinical Immunology, 2010). However, because this target encompasses the entire immune apparatus, pharmacological modulation carries significant risks of systemic immunosuppression and increased susceptibility to infection. Understanding the interplay between these diverse components is crucial for developing precision medicines that can selectively dampen pathological inflammation without compromising overall host immunity.
Broad-spectrum modulation of gene transcription, cytokine production, and leukocyte proliferation and activation (Journal of Allergy and Clinical Immunology, 2010).
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