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pmid:37422617

CD8 + T-cell marker genes reveal different immune subtypes of oral lichen planus by integrating single-cell RNA-seq and bulk RNA-sequencing.

Jinhao Zhang · Gaoge Peng · Hao Chi · Jinyan Yang · Xixi Xie · Guobin Song · Lisa Jia Tran · Zhijia Xia · Gang Tian

BMC oral health · 2023 doi:10.1186/s12903-023-03138-0

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

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title
CD8 + T-cell marker genes reveal different immune subtypes of oral lichen planus by integrating single-cell RNA-seq and bulk RNA-sequencing.
doi
10.1186/s12903-023-03138-0
pmid
37422617
authors array · 9 items
[0]
Jinhao Zhang
[1]
Gaoge Peng
[2]
Hao Chi
[3]
Jinyan Yang
[4]
Xixi Xie
[5]
Guobin Song
[6]
Lisa Jia Tran
[7]
Zhijia Xia
[8]
Gang Tian
journal
BMC oral health
year
2023
abstract
BACKGROUND: Oral lichen planus (OLP) is a local autoimmune disease induced by T-cell dysfunction that frequently affects middle-aged or elderly people, with a higher prevalence in women. CD8 + T cells, also known as killer T cells, play an important role in the progression and persistence of OLP. In order to identify different OLP subtypes associated with CD8 + T cell pathogenesis, consensus clustering was used. METHODS: In this study, we preprocessed and downscaled the OLP single-cell dataset GSE211630 cohort downloaded from Gene Expression Omnibus (GEO) to finally obtain the marker genes of CD8 + T cells. Based on the expression of marker genes, we classified OLP patients into CMGs subtypes using unsupervised clustering analysis. The gene expression profiles were analyzed by WGCNA using the "WGCNA" R package based on the clinical disease traits and typing results, and 108 CD8 + T-cell related OLP pathogenicity-related genes were obtained from the intersection. Patients were once again classified into gene subtypes based on intersection gene expression using unsupervised clustering analysis. RESULTS: After obtaining the intersecting genes of CD8 + T cells related to pathogenesis, OLP patients can be precisely classified into two different subtypes based on unsupervised clustering analysis, and subtype B has better immune infiltration results, providing clinicians with a reference for personalized treatment. CONCLUSIONS: Classification of OLP into different subtypes improve our current understanding of the underlying pathogenesis of OLP and provides new insights for future studies.
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With 11 CMGs expression profiles, we used an unsupervised clustering algorithm(“ConsensusClusterPlus” R package) [21] with 1,000 iterations to classify 14 OLP samples(Including samples GSM946260, GSM946261, GSM946262, GSM946263, GSM946264, GSM946265, GSM946266 of dataset GSE38616 and GSM260095, GSM260096, GSM260097, GSM260098, GSM260099, GSM260100, GSM260101 of dataset GSE52130)into 2 clusters.
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sections[7] "Unsupervised clustering of OLP patients" paragraph 2
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With 11 CMGs expression profiles, we used an unsupervised clustering algorithm(“ConsensusClusterPlus” R package) [21] with 1,000 iterations to classify 14 OLP samples(Including samples GSM946260, GSM946261, GSM946262, GSM946263, GSM946264, GSM946265, GSM946266 of dataset GSE38616 and GSM260095, GSM260096, GSM260097, GSM260098, GSM260099, GSM260100, GSM260101 of dataset GSE52130)into 2 clusters.
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Unsupervised consensus clustering of CD8 + T-cell-related marker-gene expression classified OLP patients into two subtypes, with subtype B showing greater immune infiltration.
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After obtaining the intersecting genes of CD8 + T cells related to pathogenesis, OLP patients can be precisely classified into two different subtypes based on unsupervised clustering analysis, and subtype B has better immune infiltration results, providing clinicians with a reference for personalized treatment.
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Unsupervised consensus clustering of CD8 + T-cell-related marker-gene expression classified OLP patients into two subtypes, with subtype B showing greater immune infiltration.
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Immune microenvironment and molecular mechanism of oral lichen planus [Single cell RNA-Seq]
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37422617", "kind": "science-record", "revision": 3, "content_hash": "sha256:bfd553af91a4b6751012c37192400ac64c950039e035b6f362de5e3c20cbc5fd", "created_at": "2026-11-01T19:02:11Z", "updated_at": "2026-11-01T21:31:08Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "CD8 + T-cell marker genes reveal different immune subtypes of oral lichen planus by integrating single-cell RNA-seq and bulk RNA-sequencing.", "doi": "10.1186/s12903-023-03138-0", "pmid": "37422617", "authors": ["Jinhao Zhang", "Gaoge Peng", "Hao Chi", "Jinyan Yang", "Xixi Xie", "Guobin Song", "Lisa Jia Tran", "Zhijia Xia", "Gang Tian"], "journal": "BMC oral health", "year": 2023, "abstract": "BACKGROUND: Oral lichen planus (OLP) is a local autoimmune disease induced by T-cell dysfunction that frequently affects middle-aged or elderly people, with a higher prevalence in women. CD8 + T cells, also known as killer T cells, play an important role in the progression and persistence of OLP. In order to identify different OLP subtypes associated with CD8 + T cell pathogenesis, consensus clustering was used.\nMETHODS: In this study, we preprocessed and downscaled the OLP single-cell dataset GSE211630 cohort downloaded from Gene Expression Omnibus (GEO) to finally obtain the marker genes of CD8 + T cells. Based on the expression of marker genes, we classified OLP patients into CMGs subtypes using unsupervised clustering analysis. The gene expression profiles were analyzed by WGCNA using the \"WGCNA\" R package based on the clinical disease traits and typing results, and 108 CD8 + T-cell related OLP pathogenicity-related genes were obtained from the intersection. Patients were once again classified into gene subtypes based on intersection gene expression using unsupervised clustering analysis.\nRESULTS: After obtaining the intersecting genes of CD8 + T cells related to pathogenesis, OLP patients can be precisely classified into two different subtypes based on unsupervised clustering analysis, and subtype B has better immune infiltration results, providing clinicians with a reference for personalized treatment.\nCONCLUSIONS: Classification of OLP into different subtypes improve our current understanding of the underlying pathogenesis of OLP and provides new insights for future studies.", "claims": [{"id": "claim-method", "statement": "With 11 CMGs expression profiles, we used an unsupervised clustering algorithm(“ConsensusClusterPlus” R package) [21] with 1,000 iterations to classify 14 OLP samples(Including samples GSM946260, GSM946261, GSM946262, GSM946263, GSM946264, GSM946265, GSM946266 of dataset GSE38616 and GSM260095, GSM260096, GSM260097, GSM260098, GSM260099, GSM260100, GSM260101 of dataset GSE52130)into 2 clusters.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37422617", "locator": "sections[7] \"Unsupervised clustering of OLP patients\" paragraph 2", "quote": "With 11 CMGs expression profiles, we used an unsupervised clustering algorithm(“ConsensusClusterPlus” R package) [21] with 1,000 iterations to classify 14 OLP samples(Including samples GSM946260, GSM946261, GSM946262, GSM946263, GSM946264, GSM946265, GSM946266 of dataset GSE38616 and GSM260095, GSM260096, GSM260097, GSM260098, GSM260099, GSM260100, GSM260101 of dataset GSE52130)into 2 clusters."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets analyzed in the current study are available in the GEO (https://www.ncbi.nlm.nih.gov/geo/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37422617", "locator": "sections[26] \"Data Availability\" paragraph 2", "quote": "The datasets analyzed in the current study are available in the GEO (https://www.ncbi.nlm.nih.gov/geo/)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Unsupervised consensus clustering of CD8 + T-cell-related marker-gene expression classified OLP patients into two subtypes, with subtype B showing greater immune infiltration.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37422617", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "After obtaining the intersecting genes of CD8 + T cells related to pathogenesis, OLP patients can be precisely classified into two different subtypes based on unsupervised clustering analysis, and subtype B has better immune infiltration results, providing clinicians with a reference for personalized treatment."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Unsupervised consensus clustering of CD8 + T-cell-related marker-gene expression classified OLP patients into two subtypes, with subtype B showing greater immune infiltration.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37422617"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE211630"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE211630"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37422617", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12903-023-03138-0", "sha256": 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"resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE38616", "version": null, "note": "The datasets analyzed in the current study are available in the GEO (https://www.ncbi.nlm.nih.gov/geo/).", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets analyzed in the current study are available in the GEO (https://www.ncbi.nlm.nih.gov/geo/).", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM946253", "GSM946254", "GSM946255", "GSM946256", "GSM946257", "GSM946258", "GSM946259", "GSM946260", "GSM946261", "GSM946262", "GSM946263", "GSM946264", "GSM946265", "GSM946266"], "sample_count": 14, "group_sizes": null, "group_sizes_basis": null, "platform": "6244", "taxon": "Homo sapiens", "title": "Expression data from primary tissue, human oral mucosa (mRNA data)", "resolution_checked_at": "2026-11-01T18:06:44Z", "resolution_check": 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"pca", "label": "Principal component analysis", "dsl_operations": ["pca_fit"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["wide_numeric_matrix"], "evidence": {"score": 0.8, "band": "high", "quote": "principal component analysis"}}, {"id": "method-2", "family": "correlation_analysis", "specific": "spearman", "label": "Correlation analysis", "dsl_operations": ["spearman_rho"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["paired_numeric_columns"], "evidence": {"score": 0.8, "band": "high", "quote": "Spearman correlation"}}, {"id": "method-3", "family": null, "specific": null, "label": "Unsupervised consensus clustering using the ConsensusClusterPlus R package", "dsl_operations": [], "missing_operations": [], "expressible": null, "parameters": {}, "data_shapes": [], "evidence": {"score": 1.0, "band": "verbatim", "quote": "With 11 CMGs expression profiles, we used an unsupervised clustering algorithm(“ConsensusClusterPlus” R package) [21] with 1,000 iterations to classify 14 OLP samples(Including samples GSM946260, GSM946261, GSM946262, GSM946263, GSM946264, GSM946265, GSM946266 of dataset GSE38616 and GSM260095, GSM260096, GSM260097, GSM260098, GSM260099, GSM260100, GSM260101 of dataset GSE52130)into 2 clusters."}}], "targets": [], "gaps": ["method.reader_named_unmapped"]}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": 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