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Omics · dataset · 2026

Table 5_Single-cell profiling of peripheral immune remodeling in BK polyomavirus–associated nephropathy after kidney transplantation.xlsx

Listed in ZivaHub and Deakin Research Online and DMU Figshare and HKU DataHub and Swinburne Figshare and DaYta Ya Rona and SUNScholarData and figshare and Loughborough Research Repository and GRANTS Data and UP Research Data Repository — shown once because both records carry DOI 10.3389/fimmu.2026.1939071.s002

<p>BK polyomavirus–associated nephropathy (BKPyVAN) remains a major cause of allograft dysfunction after kidney transplantation.

Description

To define peripheral immune signatures associated with distinct clinical states of BKPyV infection, we performed single-cell RNA sequencing of peripheral blood mononuclear cells from kidney transplant recipients across three clinical states: stable graft function (n = 1), BKPyV DNAemia (n = 2), and biopsy-proven BKPyVAN (n = 3).

We identified 17 immune cell populations and observed remodeling of both the innate and adaptive compartments. Monocyte subsets differed across clinical states, with CD16<sup>+</sup> non-classical monocytes enriched in BKPyV DNAemia and inflammatory monocytes more abundant in BKPyVAN. CD8<sup>+</sup> T-cell frequency was higher in BKPyVAN than in BKPyV DNAemia, while NK-cell frequency was lower in BKPyV DNAemia and BKPyVAN than in Stable, consistent with altered antiviral surveillance.

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A rare but transcriptionally distinct population, termed Activated Effector Cells (AECs), comprised only 0.60% of cells in BKPyVAN (104 of 17,238 cells) yet accounted for 12.15% of cluster-associated marker calls, the highest among the 17 populations, and displayed marked enrichment of cell cycle and RNA metabolic pathways. Across multiple lineages, AUC-based gene set enrichment analysis revealed convergent activation of RNA processing and intracellular transport pathways.

Pseudobulk differential expression and permutation testing supported condition-associated transcriptional signatures, and leading-edge gene analysis identified candidate transcriptional readouts, including cell cycle regulators, inflammatory mediators, and RNA processing genes, with potential utility for blood-based monitoring. These findings reveal peripheral immune remodeling across the clinical states of BK polyomavirus infection and highlight the value of resolving rare, transcriptionally distinct immune populations, providing a rationale for noninvasive, transcriptomics-informed monitoring and risk stratification strategies.</p>

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Immunology 72% · RNA sequencing 75% · Sequencing 75% · Tabular 65%
Provenance · 11 source records, 77 field assertions
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