<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Liu Q</submitter><pubmed_abstract>Lupus nephritis (LN), the most severe complication of systemic lupus erythematosus (SLE), arises from systemic immune dysregulation and renal damage. While renal immune perturbations are well-studied, systemic signatures specific to LN pathogenesis remain unclear. Integrated single-cell RNA and immune repertoire analysis of 177,259 peripheral blood mononuclear cells (PBMCs) from healthy donors and SLE patients (including active LN and non-nephritis controls) revealed LN-specific circulating immune signatures, including κ light-chain preference in naive B cells and distinct clonal expansion in CD8&lt;sup>+&lt;/sup> effector T cells. These clonally expanded CD8&lt;sup>+&lt;/sup> effector T cells exhibited transcriptional variations indicating increased migratory capacity and exhaustion, along with prefe</pubmed_abstract><journal>Communications biology</journal><pagination>155</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12868680</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Single-cell profiling unveils nephritis-related circulating immunological signatures in systemic lupus erythematosus patients.</pubmed_title><pmcid>PMC12868680</pmcid><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Xie X</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Li P</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Hao S</pubmed_authors><pubmed_authors>Bai X</pubmed_authors><pubmed_authors>Cai G</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Cheng T</pubmed_authors><pubmed_authors>Lin H</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Guo C</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Deng Y</pubmed_authors><pubmed_authors>Shang S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell profiling unveils nephritis-related circulating immunological signatures in systemic lupus erythematosus patients.</name><description>Lupus nephritis (LN), the most severe complication of systemic lupus erythematosus (SLE), arises from systemic immune dysregulation and renal damage. While renal immune perturbations are well-studied, systemic signatures specific to LN pathogenesis remain unclear. Integrated single-cell RNA and immune repertoire analysis of 177,259 peripheral blood mononuclear cells (PBMCs) from healthy donors and SLE patients (including active LN and non-nephritis controls) revealed LN-specific circulating immune signatures, including κ light-chain preference in naive B cells and distinct clonal expansion in CD8&lt;sup>+&lt;/sup> effector T cells. These clonally expanded CD8&lt;sup>+&lt;/sup> effector T cells exhibited transcriptional variations indicating increased migratory capacity and exhaustion, along with prefe</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-15T06:07:51.282Z</modification><creation>2026-07-01T03:07:45.47Z</creation></dates><accession>S-EPMC12868680</accession><cross_references><pubmed>41490945</pubmed><doi>10.1038/s42003-025-09431-8</doi></cross_references></HashMap>