scholarly journals Novel biomarkers for the assessment of paediatric systemic lupus erythematosus nephritis

2017 ◽  
Vol 188 (1) ◽  
pp. 79-85 ◽  
Author(s):  
A. Koutsonikoli ◽  
M. Trachana ◽  
E. Farmaki ◽  
V. Tzimouli ◽  
P. Pratsidou-Gertsi ◽  
...  
2015 ◽  
Vol 16 (8) ◽  
pp. 16953-16965 ◽  
Author(s):  
Isabelle Duroux-Richard ◽  
Jimena Cuenca ◽  
Clara Ponsolles ◽  
Alejandro Badilla Piñeiro ◽  
Fernando Gonzalez ◽  
...  

Author(s):  
Hani Susianti ◽  
Kusworini Handono

Lupus Nephritis (LN) is one of the serious clinical manifestation of Systemic Lupus Erythematosus (SLE). Early detection and treatmentof renal activity may spare patients from renal damage. Conventional biomarkers such as urine sediment, proteinuria, creatinine, antidsDNA antibody and their complement levels are not specific and sensitive enough in detecting the ongoing disease activity in the lupuskidneys and early relapse of nephritis. Renal biopsy is the gold standard in providing information on the histopathology of LN, but isinvasive and it should take a serial of biopsies making it impractical when monitoring LN. Thus, some novel biomarkers are necessary toenhance the diagnostic accuracy and sensitivity of lupus renal disease, prognostic stratification, monitoring of treatment response anddetection of early renal flares as well. Some novel biomarkers have been studied in LN, however, validation on a large scale of patientswith different ethnic backgrounds is still needed.


Rheumatology ◽  
2008 ◽  
Vol 48 (5) ◽  
pp. 497-501 ◽  
Author(s):  
M. Al ◽  
L. Ng ◽  
P. Tyrrell ◽  
J. Bargman ◽  
T. Bradley ◽  
...  

Oncotarget ◽  
2017 ◽  
Vol 8 (14) ◽  
pp. 23650-23663 ◽  
Author(s):  
Guo-Cui Wu ◽  
Jun Li ◽  
Rui-Xue Leng ◽  
Xiang-Pei Li ◽  
Xiao-Mei Li ◽  
...  

F1000Research ◽  
2019 ◽  
Vol 8 ◽  
pp. 368 ◽  
Author(s):  
David S. Pisetsky

Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease whose pathogenesis can be conceptualized by a model based on a central role for immune complexes (ICs) between antinuclear antibodies and nucleic acids. According to this model, ICs can promote pathogenesis by two main mechanisms: deposition in the tissue to incite local inflammation and interaction with cells of the innate immune system to stimulate the production of cytokines, most prominently type 1 interferon. The latter stimulation results from the uptake of DNA and RNA in the form of ICs into cells and subsequent signaling by internal nucleic acid sensors for DNA and RNA. These sensors are likely important for the response to intracellular infection, although they may also be triggered during cell stress or injury by DNA or RNA aberrantly present in the cytoplasm. For IC formation, a source of extracellular DNA and RNA is essential. The current model of SLE posits that cell death is the origin of the nucleic acids in the ICs and that impairment of clearance mechanisms increases the amount of nuclear material in the extracellular space. This model of SLE is important since it points to new approaches to therapy; agents targeting interferon or the interferon receptor are examples of therapeutic approaches derived from this model. Future studies will explore novel biomarkers to monitor the operation of these mechanisms and to elucidate other steps in pathogenesis that can be targeted for therapy.


2021 ◽  
Vol 22 (5) ◽  
Author(s):  
Chunli Rong ◽  
Huafeng Xu ◽  
Changxin Yan ◽  
Feng Wei ◽  
Haizhou Zhou ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document