Currently, over 350 million people worldwide live with chronic inflammatory diseases, facing a range of complications that severely impact their quality of life. Among these complications is amyloidosis, a group of diseases characterized by the extracellular deposition of insoluble amyloid fibrils that disrupt tissue structure and function. One specific form, amyloid A (AA) amyloidosis, is closely linked to chronic inflammatory conditions such as rheumatoid arthritis (RA), Familial Mediterranean Fever (FMF), Crohn’s disease, and chronic infections. In this issue of , Losa et al, shows that the inflammasome adaptor ASC plays an important role in the pathogenesis of AA amyloidosis, and suggests a potential immunotherapy for treating the disease (Losa et al, 2024).
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11393065 | PMC |
http://dx.doi.org/10.1038/s44321-024-00109-y | DOI Listing |
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