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Mice lacking the membrane tyrosine kinase c-mer have been shown to have altered macro-phage cytokine production and defective phagocytosis of apoptotic cells despite normal phagocytosis of other particles. We show here that c-mer-deficient mice have impaired clearance of infused apoptotic cells and that they develop progressive lupus-like autoimmunity, with antibodies to chromatin, DNA, and IgG. The autoimmunity appears to be driven by endogenous antigens, with little polyclonal B cell activation. These mice should be an excellent model for studying the role of apoptotic debris as an immunogenic stimulus for systemic autoimmunity.
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http://dx.doi.org/10.1084/jem.20012094 | DOI Listing |
Scand J Immunol
September 2025
University Hospital "St. Ivan Rilski, " Laboratory of Clinical Immunology, Sofia, Bulgaria.
Systemic lupus erythematosus (SLE) is an example of an autoimmune disease manifesting itself in an aberrated immune response directed against nuclear, cytoplasmic and cell-surface antigens. Among patients, symptoms are frequently intensified in females during their active reproductive years, pinpointing the interaction between reproductive and immune systems. Hence, it is urgent to address the question of how SLE can influence female fertility and the impact of hormones on disease manifestation.
View Article and Find Full Text PDFBiomolecules
July 2025
Institute of Basic Research in Clinical Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou 310000, China.
Systemic lupus erythematosus (SLE) is characterized by autoimmune dysregulation, elevated autoantibody production, and persistent inflammation, predisposing patients to atherosclerosis (AS). Atherogenesis is dependent on lipid homeostasis and inflammatory processes, with the formation of lipid-laden, macrophage-derived foam cells (MDFC) essential for atherosclerotic lesion progression. Elevated cholesterol levels within lipid rafts trigger heightened pro-inflammatory responses in macrophages via Toll-like receptor 9 (TLR9).
View Article and Find Full Text PDFFront Pediatr
July 2025
Department of Pediatric Allergy and Immunology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Haploinsufficiency of A20 (HA20), caused by mutations, is a rare autoinflammatory syndrome characterized by highly variable, multisystem manifestations that often delay recognition and definitive care. The A20 protein restrains NF-κB-mediated pro-inflammatory signaling; therefore, loss-of-function variants unleash widespread inflammation that can involve virtually any organ. Fewer than 200 cases have been reported worldwide; thus, clinicians have limited phenotype-specific guidance.
View Article and Find Full Text PDFArthritis Rheumatol
August 2025
Department of Internal Medicine, Division of Rheumatology, University of Michigan, Ann Arbor, Michigan, United States.
Objective: Keratinocyte-derived interferon kappa (IFN-κ) is chronically overexpressed in human non-lesional systemic lupus erythematosus (SLE) skin. Recent evidence suggests that epidermal signals instruct the immune system in SLE, but whether epidermal IFN-κ alone is sufficient to drive lupus phenotypes has not been investigated. This study aimed to identify whether epidermal-specific overexpression of Interferon kappa (Ifnk) results in lupus-like cutaneous and systemic inflammation.
View Article and Find Full Text PDFCureus
June 2025
Department of Nephrology, Centre Hospitalier Universitaire d'Orléans, Orléans, FRA.
A 41-year-old woman without significant medical history was admitted for edema and a 10 kg weight gain. Two months earlier, she had experienced a flu-like syndrome treated with amoxicillin. At admission, she presented with severe hypertension and stage 1 acute kidney injury.
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