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Beyond Autoantibodies: The Predictive and Pathogenic Role of Pro-Inflammatory Cytokines in Type 1 Diabetes | ||
| Iranian Journal of Immunology | ||
| دوره 23، شماره 2، شهریور 2026، صفحه 1-1 | ||
| نوع مقاله: Review Article | ||
| شناسه دیجیتال (DOI): 10.22034/iji.2026.108390.3096 | ||
| نویسندگان | ||
| Anil Philip Kunnath* 1؛ Sorfina Ahmad Hilmi2؛ Dinesh Kumar1 | ||
| 1IMU University | ||
| 2IMU University Malaysia | ||
| چکیده | ||
| Type 1 diabetes (T1DM) is an autoimmune disorder marked by a characteristic dysfunction of insulin-secreting beta-cells in the pancreatic islets. This destructive process is not a single event but a chronic inflammatory cascade, propelled by immune cells—including T-lymphocytes and macrophages—that release potent pro-inflammatory cytokines. This review delves into the growing body of evidence implicating specific inflammation-promoting mediators—including Interleukin-1β (IL-1β), Tumor Necrosis Factor-α (TNF-α) and Interferon-γ (IFN-γ) —as master regulators of beta-cell death. We also explore how modern analytical techniques enable precise mapping of cytokine patterns in the blood, revealing a dynamic and ongoing disease process long that precedes clinical symptoms onset. By weaving together findings from clinical and preclinical studies, this article argues that profiling these inflammatory signals provides a crucial real-time, functional readout of autoimmune activity that complements traditional, static autoantibody measurements. We conclude by discussing the significant potential of integrating cytokine data into existing models to create more robust risk stratification tools and to pave the way for interventions that could intercept the disease pathway before critical beta-cell mass is lost. | ||
| کلیدواژهها | ||
| Pro-inflammatory cytokines؛ β cells؛ Type 1 diabetes؛ Reactive oxygen species | ||
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آمار تعداد مشاهده مقاله: 31 |
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