<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>47(1)</volume><submitter>Yang X</submitter><pubmed_abstract>Lupus nephritis (LN) is a frequent and serious complication of systemic lupus erythemosus (SLE). Both innate and adaptive immunity play essential roles in the initiation and progression of LN. B-lymphocyte stimulator (BLYS) and a proliferation-inducing ligand (APRIL), members of the tumor necrosis factor superfamily, bind to receptors such as B-cell activating factor receptor 3 (BR3), transmembrane activator and CAML interactor protein (TACI), and B-cell maturation antigen (BCMA). BLYS and APRIL are often overexpressed in LN, showing a positive correlation with disease activity. Therapeutic targeting of BLYS/APRIL has demonstrated efficacy in reducing LN activity. Traditional immunosuppressants often have multiple contraindications and side effects due to their broad immune-suppressing eff</pubmed_abstract><journal>Renal failure</journal><pagination>2561791</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12624907</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Biological targeted therapy for lupus nephritis-the role of BLYS and APRIL.</pubmed_title><pmcid>PMC12624907</pmcid><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Lv J</pubmed_authors><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Liu XJ</pubmed_authors><pubmed_authors>Deng Q</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Wen D</pubmed_authors><pubmed_authors>Li L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biological targeted therapy for lupus nephritis-the role of BLYS and APRIL.</name><description>Lupus nephritis (LN) is a frequent and serious complication of systemic lupus erythemosus (SLE). Both innate and adaptive immunity play essential roles in the initiation and progression of LN. B-lymphocyte stimulator (BLYS) and a proliferation-inducing ligand (APRIL), members of the tumor necrosis factor superfamily, bind to receptors such as B-cell activating factor receptor 3 (BR3), transmembrane activator and CAML interactor protein (TACI), and B-cell maturation antigen (BCMA). BLYS and APRIL are often overexpressed in LN, showing a positive correlation with disease activity. Therapeutic targeting of BLYS/APRIL has demonstrated efficacy in reducing LN activity. Traditional immunosuppressants often have multiple contraindications and side effects due to their broad immune-suppressing eff</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-05T16:33:38.428Z</modification><creation>2026-05-18T03:13:03.591Z</creation></dates><accession>S-EPMC12624907</accession><cross_references><pubmed>41249101</pubmed><doi>10.1080/0886022X.2025.2561791</doi></cross_references></HashMap>