Background: Takayasu arteritis (TA) is a large-vessel vasculitis with an incompletely understood pathogenesis, in which genetic factors are thought to play an important role. Cytokine-mediated immune pathways, particularly those involving Th1 and Th17 responses, have been implicated in the immunopathogenesis of TA, mak...
Maja Stojanović, Ž. Jovičić, Ana Drazic et al.· Immuno· 0 citations
Granulomatous-lymphocytic interstitial lung disease (GLILD) develops in 10–30% of patients with common variable immunodeficiency (CVID) as a consequence of immune dysregulation. Therefore, immunoglobulin (Ig) M, produced by apoptosis-resistant plasmablasts in extrafollicular sites in the lungs, and serum soluble in...
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 (IEI) comprise a broad spectrum of disorders caused by genetic defects impairing innate and adaptive immunity, non-hematopoietic cell–mediated responses, and immune regulation. The Clinic of Allergy and Immunology at the University Clinical Center of Serbia serves as a national reference cente...
Maja Stojanović· Journal of Human Immunity· 0 citations
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