Results 51 to 60 of about 9,499 (196)
The Intensity of PLA2R and C4d Immunoexpression in Primary Membranous Nephropathy
INTRODUCTION[|]Antibodies against the phospholipase A2 receptor (PLA2R) on podocyte membranes result in the formation of immune complexes that cause loss of function of the glomerular basement membrane in primary membranous nephropathy (PMN). It has also
Deniz Filinte +5 more
doaj +1 more source
ABSTRACT Background and Aims Long COVID, also known as post‐acute sequelae of SARS‐CoV‐2 infection (PASC), is a multisystem condition characterized by persistent symptoms that continue beyond the acute phase of infection. Growing evidence indicates that sustained immune dysregulation involving cytokine‐mediated inflammation, complement activation ...
Emmanuel Ifeanyi Obeagu
wiley +1 more source
Study of the variables associated with local complement activation in IgA nephropathy
Objectives: 1. To identify the variables that are associated with urinary levels of properdin, MBL, C4d, and C5b-9 in patients with idiopathic IgA nephropathy. 2. To analyse whether urinary levels of MBL and/or C4d are useful for identifying the presence
Alfons Segarra-Medrano +6 more
doaj +1 more source
Lupus nephritis (LN), occurring in approximately 50% of individuals with systemic lupus erythematosus (SLE), significantly influences therapy and prognosis.
Mahmoud M. Elnokeety +2 more
doaj +1 more source
Refractory ascites (RA) post‐pediatric LT is stratified into two subtypes: Type I (portal hypertension‐driven) and Type II (immune‐mediated). Type I is linked to low GRWR and hypersplenism, while Type II involves ABO incompatibility and early T‐cell activation (elevated sIL‐2R). Type II increases rejection risk (OR = 2.212).
Bingran Wang +15 more
wiley +1 more source
Analyses of the clinical and immunological characteristics of patients with lupus erythematosus
Background: Lupus erythematosus (LE) is a broad-spectrum, heterogeneous disease. At one end of the spectrum is the cutaneous LE (CLE) without systemic involvement, and at the other end is the systemic LE (SLE) with multisystem involvement.
Min Deng +4 more
doaj +1 more source
Serum galactose‐deficient IgA1 levels at 3 and 6 months predicted recurrent IgA nephropathy after kidney transplantation. Recipients without recurrence showed a rapid decline in galactose‐deficient IgA1 after transplantation. Early identification of recurrence risk provided a potential window for targeted post‐transplant intervention.
Ronghai Deng +10 more
wiley +1 more source
İGA nefropatisinde mezengiyal ve arteriolar C4D depolanmasının prognoz ile ilişkisi
İmmunglobulin A (IgA) nefropatisi, bütün dünyada en sık görülen primer glomerülonefrittir. IgA nefropatisi geniş bir klinik çeşitlilik göstermektedir. Asemptomatik hematüriden hızlı ilerleyici glomerülonefrite kadar farklı şiddetlerde klinikle prezente ...
YASEMİN AKTAŞ SAVRUN
core +1 more source
Background We aimed to investigate the involvement of the classical/lectin complement pathway in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) by exploring the complement activation fragment C4d in association to AAV activity ...
Anna Juto +8 more
doaj +1 more source
Case series: Kikuchi‐Fujimoto disease with diagnostic overlap
Kikuchi‐Fujimoto disease (KFD) is a rare, self‐limiting necrotizing lymphadenitis that poses significant diagnostic challenges due to its overlap with tuberculosis, systemic lupus erythematosus (SLE), and malignancy. We present four cases highlighting distinct diagnostic complexities: KFD mimicking tuberculosis with concomitant latent TB infection and ...
Ecem Kalemoglu +6 more
wiley +1 more source

