Abstract
Type 1 diabetes ( T1D) is a chronic, progressive autoinflammatory disorder resulting from the breakdown of selftolerance and unrestrained ss cell-reactive immune response. Activation of immune cells is initiated in islet and amplified in lymphoid tissues, especially those pancreatic draining lymph nodes (PLNs). The knowledge of PLNs as the hub of aberrant immune response is continuously being replenished and renewed. Here we provide a PLN-centered view of T1D pathogenesis and emphasize that PLNs integrate signal inputs from the pancreas, gut, viral infection or peripheral circulation, undergo immune remodeling within the local microenvironment and export effector cell components into pancreas to affect T1D progression. In accordance, we suggest that T1D intervention can be implemented by three major ways: cutting off the signal inputs into PLNs (reduce inflammatory ss cell damage, enhance gut integrity and control pathogenic viral infections), modulating the immune activation status of PLNs and blocking the outputs of PLNs towards pancreatic islets. Given the dynamic and complex nature of T1D etiology, the corresponding intervention strategy is thus required to be comprehensive to ensure optimal therapeutic efficacy.
| Original language | English |
|---|---|
| Article number | 156 |
| Number of pages | 14 |
| Journal | Cell and Bioscience |
| Volume | 13 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 28 Aug 2023 |
| Externally published | Yes |
Keywords
- Pancreatic draining lymph nodes (PLNs)
- PLN remodeling
- Signal inputs
- Signal outputs
- Type 1 diabetes (T1D)
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