scholarly journals Murine Membranous Nephropathy: Immunization with α3(IV) Collagen Fragment Induces Subepithelial Immune Complexes and FcγR-Independent Nephrotic Syndrome

2012 ◽  
Vol 188 (7) ◽  
pp. 3268-3277 ◽  
Author(s):  
Jun-Jun Zhang ◽  
Mahdi Malekpour ◽  
Wentian Luo ◽  
Linna Ge ◽  
Florina Olaru ◽  
...  
Vestnik ◽  
2021 ◽  
pp. 155-157
Author(s):  
Л.П. Мамедова ◽  
А.К. Беисбекова

Мембранозная нефропатия является иммунологически обусловленной не воспалительной гломерулопатией, имеет прогрессирующее стадийное течение и характеризуется дистрофическими и склеротическими процессами. Мембранозная нефропатия - это поражение почечных клубочков (основные функциональные единицы почек), возникающее вследствие оседания на стенках почечных капилляров иммунных комплексов. Это приводит к утолщению и дальнейшему расслоению базальных мембран и стенок сосудов в клубочках. Основным клиническим проявлением МН является нефротический синдром (отеки по всему телу, наличие белка в моче и высокий холестерин в крови). Membranous nephropathy is an immunologically determined non-inflammatory glomerulopathy, has a progressive stage course and is characterized by dystrophic and sclerotic processes. Membranous nephropathy is a lesion of the renal glomeruli (the main functional units of the kidneys) that occurs due to the settling of immune complexes on the walls of the renal capillaries. This leads to thickening and further delamination of the basal membranes and vascular walls in the glomeruli. The main clinical manifestation of MN is nephrotic syndrome (edema throughout the body, the presence of protein in the urine and high cholesterol in the blood).


2021 ◽  
Vol 14 (3) ◽  
pp. e240288
Author(s):  
Gabriela F Santos ◽  
Paul Ellis ◽  
Daniela Farrugia ◽  
Alice M Turner

We report a 64-year-old caucasian woman diagnosed with membranous nephropathy secondary to alpha-1 antitrypsin deficiency (AATD). AATD is a rare autosomal codominant genetic disorder. Its clinical manifestations are mostly observed in the lungs, with early-onset emphysema. Nephropathy due to AATD is still very rare and only a few cohort studies have been reported. It has been recognised that alpha-1 antitrypsin has a protective role in the kidneys which enhances the possibility of development of kidney failure, such as nephrotic syndrome, in cases of AATD. Further clinical investigation is needed to understand the relationship between the development of nephropathy, namely membranous nephropathy, and AATD.


1997 ◽  
Vol 58 (8) ◽  
pp. 1864-1868 ◽  
Author(s):  
Kentaro EMOTO ◽  
Tadateru TAKAHASHI ◽  
Yoshitaka KATO ◽  
Takayuki NOMIMURA ◽  
Ichiro OMORI ◽  
...  

Pharmacology ◽  
2013 ◽  
Vol 91 (5-6) ◽  
pp. 259-266 ◽  
Author(s):  
Hang Yuan ◽  
Nian Liu ◽  
Guang-Dong Sun ◽  
Ye Jia ◽  
Ping Luo ◽  
...  

2010 ◽  
pp. 3985-3988
Author(s):  
Dwomoa Adu

Membranous nephropathy, which accounts for 20 to 30% of cases of the nephrotic syndrome in adults, is defined histologically by the presence of subepithelial immune deposits on the outer surface of the glomerular basement membrane. The immune mechanisms that lead to this are uncertain, and most cases are of unknown cause (idiopathic), but the condition can be associated with autoimmune diseases (systemic lupus erythematosus), malignancy (in 10% of cases, most commonly lung and prostate cancer), drugs, and infections....


2020 ◽  
Vol 147 ◽  
pp. 104359 ◽  
Author(s):  
Jun Zhang ◽  
Dan Luo ◽  
Zhiming Lin ◽  
Wenying Zhou ◽  
Jialing Rao ◽  
...  

1978 ◽  
Vol 298 (3) ◽  
pp. 126-129 ◽  
Author(s):  
Roland J. Levinsky ◽  
Peter N. Malleson ◽  
T. Martin Barratt ◽  
John F. Soothill

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