The nature of a typical clinical test for lupus nephritis (LN), an inflammation of the kidneys and a leading cause of mortality in lupus patients, is fraught with difficulty. The invasive renal biopsy can be painful and may cause kidney damage. Unfortunately, 60% of patients with the often-disabling autoimmune disorder systemic lupus erythematosus (SLE) will face this burden as they advance into potentially fatal lupus nephritis.
“Given the heterogenetic nature and unmet needs in precision diagnosis and classification of SLE/LN patients for personalized medication, identification of novel biomarkers, particularly in the form of a biomarker panel, is of paramount importance,” reports Tianfu Wu, University of Houston associate professor of biomedical engineering, in the journal Frontiers in Immunology.
So, Wu and his team met that need using the large-scale study of proteins involved in the immune system, known as immunoproteomics, combined with bioinformatics, which combines gene expression data with computer storage and analysis.
A total of 300 immunoglobulin-binding proteins were discovered in the screening, among which 77 proteins were detectable only in LN samples. Bioinformatics-assisted selection allowed the team to further identify ten potential immunoglobulin-binding proteins, which form circulating immune complexes (ICx) as potential biomarkers in LN.
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