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Updated: Aug 13, 2026

VDJ-Seq: Deep Sequencing Analysis of Rearranged Immunoglobulin Heavy Chain Gene to Reveal Clonal Evolution Patterns of B Cell Lymphoma
Published on: December 28, 2015
scRNA+VDJ-seq in SLE: Insights into autoreactive T and B cell subsets, features, and therapeutic applications
Hailin Zou1, Guangtian Tang1, Xueqi Hao1
1Department of Immunology, Center of Immuno-molecular Engineering, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi 563000, Guizhou Province, PR China.
None:
The adaptive autoimmune process in SLE is complex, and conventional techniques cannot resolve disease-associated T/B lymphocyte clones at a single-cell granularity. Single-cell RNA sequencing combined with single-cell V(D)J sequencing (scRNA+VDJ-seq) enables simultaneous profiling of cellular transcriptomes and TCR/BCR repertoires. This review highlights recent advances in scRNA+VDJ-seq in SLE and related autoimmune disorders, elucidating the link between receptor clonality, gene expression, and effector phenotypes. It delineates clonal expansion, biased V(D)J usage, and aberrant exhaustion in SLE, and compares T/B cell immune phenotypes across lupus nephritis, RA, pSS, and AS. The review also summarizes CD19 CAR-T and PD-1 agonist applications. Furthermore, it discusses AI integration with scRNA+VDJ-seq to analyze autoreactive T/B cells in SLE: from data integration to clinical translation, and assesses the clinical translational potential of this technology, offering novel targets and strategies for SLE diagnosis, personalized treatment, and prognosis.
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