Enteropathy represents one of the most frequent noninfectious clinical manifestations of common variable immunodeficiency (CVID), with underlying pathophysiological mechanisms that remain insufficiently understood. Patients with CVID-associated enteropathy (CVID-E) have a significantly higher frequency of liver inv...
Jelena Ljubicic, Ivan Ranković, U. Karić et al.· Journal of Human Immunity· 0 citations
Sarcoidosis and granulomatosis with polyangiitis (GPA) are the most common non-infectious causes of granulomatous lung disease. However, they can sometimes be difficult to distinguish due to overlapping clinical, radiological, and histopathological features. A 54-year-old man was considered to have sarcoidosis in 2018....
Aleksandra Dašić, Dragan Vasin, Maja Stojanović et al.· Diseases· 0 citations
Undifferentiated systemic autoinflammatory diseases (uSAID) are characterized by recurrent fever and systemic inflammation without a definitive molecular diagnosis. Increasing use of next-generation sequencing frequently identifies variants of uncertain significance (VUS), further complicating diagnosis. Therefore,...
Anica Kisić, Rada Mišković, Srđa Janković et al.· Journal of Human Immunity· 0 citations
Evaluated biomarkers of immunoglobulin (Ig) M and sIL-2R showed a potential role for IgM in disease pathogenesis, and higher sIL-2R levels reinforce the concept of immune dysregulation as a key feature of this CVID phenotype.
Aleksandra Dašić, Rada Mišković, S. Janković et al.· Journal of Human Immunity· 0 citations
22q11.2 deletion syndrome (22q11.2 DS) is one of the most common microdeletion syndromes, characterized by congenital anomalies and variable immune dysfunction secondary to thymic hypoplasia. The resulting immune dysregulation frequently predisposes affected individuals to autoimmune manifestations, including immun...
Ana Drazic, S. Pasic, Maja Stojanović et al.· Journal of Human Immunity· 0 citations
Inborn errors of immunity (IEIs) frequently present with rheumatologic and autoimmune manifestations that closely mimic common polygenic conditions, including systemic lupus erythematosus, juvenile idiopathic arthritis, and vasculitis, posing significant challenges to early recognition and diagnosis. Current data indic...
Rada Mišković· Journal of Human Immunity· 0 citations
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