Introduction: Juvenile systemic lupus erythematosus (jsle) is an autoimmune disease that develops as a result of multi-level immune dysregulation, including the interferon pathway. nephropathy develops at an early stage and eventually affects 90% of patients. a renal biopsy allows one to classify lupus nephritis and determine the proper treatment. Biopsy assessment should be done not only in a light microscope but also in a transmission electron microscope (teM). its usage may reveal the presence of intracellular tubuloreticular inclusions (tris), considered as a morphological marker of interferon hyperactivity.Material and methods: renal biopsies of 10 children with jsle and nephropathy were analyzed in teM. the location, structure, and size of tris were assessed. demographic data, nephropathy manifestation, non-renal symptoms, and serological activity of lupus were analyzed.Results: all the patients were female with an average onset at 12.7 years of age and met sle criteria. nephropathy manifested with proteinuria (n = 10) and hematuria (n = 6). Glomerular filtration rate (GFr) was normal in all patients. in three children with early disease onset, it manifested with hematological disorders. tris were revealed in 7 biopsies, with the highest expression in the youngest children, with peripheral cytopenia, membranous glomerulonephritis, and lupus nephritis.Conclusions: demonstration of tris in renal biopsies of children with juvenile systemic lupus may confirm the diagnosis of lupus nephritis and is a sign of involvement of the interferon pathway at the early stage of the disease.