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چکیده
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The global surge in diabetes presents a significant healthcare challenge. Viral infections complicate diabetes by influencing systemic metabolism and disrupting glycemic control in type 2 diabetes (T2D). High glucose levels impair macrophage activity, raising the risk of chronic infections. Viral-induced type-I immune responses initiate insulin resistance, which affects muscle, liver, and pancreatic functions. Diabetogenic viruses impair pancreatic cells or affect gut microbiota. Viral survival tactics disrupt antigen presentation and use viral miRNAs to target diabetes-related gene expression. The hidden association between latent viruses, particularly herpesviruses like Human Cytomegalovirus (HCMV), and diabetes is explored, emphasizing CMV's role in type 1 diabetes (T1D) pathogenesis. Inflammatory pathways triggered by viral infections play a critical role in islet-specific autoimmunity and the development of T1D. The HCMV’s pervasive reach, from local areas to the entire body, involves infected monocytes infiltrating organs, persisting in the bone marrow, and enabling virus spread during reactivation events. When a viral infection occurs, the immune system mounts a type 1 response characterized by the activation of CD4+ T-cells and the production of pro-inflammatory cytokines, such as interferon-gamma (IFN-γ) and tumor necrosis factor-alpha (TNF-α). These cytokines can lead to the recruitment of immune cells to pancreatic islets, resulting in inflammation and damage to insulinproducing beta cells. Furthermore, the chronic inflammation caused by sustained cytokine release can impair insulin signaling pathways. Specifically, pro-inflammatory cytokines interfere with insulin receptor substrate (IRS) proteins, leading to decreased insulin sensitivity in peripheral tissues such as muscle and adipose tissue. This cascade of events ultimately contributes to the development of insulin resistance, setting the stage for T2D. This investigation highlights the complex relationship between viral infections and diabetes. Research indicates that viral infections can increase the risk of developing T2D.
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