Tooluniverse Immune Repertoire Analysis

ToolUniverse Immune Repertoire Analysis

Comprehensive skill for analyzing T-cell receptor (TCR) and B-cell receptor (BCR) repertoire sequencing data to characterize adaptive immune responses, clonal expansion, and antigen specificity.

Domain Reasoning

Repertoire diversity reflects immune history. High clonality — a few clones dominating — indicates antigen-driven expansion, as seen in active infection, tumor-infiltrating lymphocytes, or chronic stimulation. Low diversity points to immunodeficiency or treatment-induced lymphopenia. Always compare observed metrics against healthy donor reference distributions before drawing conclusions; a Shannon entropy of 7 is unremarkable in a healthy adult but alarming post-chemotherapy.

LOOK UP DON'T GUESS

• Clonotype frequency thresholds, CDR3 length ranges, and convergence ratios: query IEDB or VDJdb; do not assume values from memory.
• Epitope specificities for expanded clones: search iedb_search_tcell_assays and BVBRC_search_epitopes; never infer antigen identity from CDR3 alone.
• V gene family usage biases in healthy donors: retrieve published reference data or query ImmPort; do not assume baseline distributions are uniform.
• Sequencing depth adequacy: compute rarefaction curves from the actual data; do not guess whether depth is sufficient.

Overview

Adaptive immune receptor repertoire sequencing (AIRR-seq) enables comprehensive profiling of T-cell and B-cell populations through high-throughput sequencing of TCR and BCR variable regions. This skill provides an 8-phase workflow for:

• Clonotype identification and tracking
• Diversity and clonality assessment
• V(D)J gene usage analysis
• CDR3 sequence characterization
• Clonal expansion and convergence detection
• Epitope specificity prediction
• Integration with single-cell phenotyping
• Longitudinal repertoire tracking

Core Workflow

Phase 1: Data Import & Clonotype Definition

Load AIRR-seq data from common formats (MiXCR, ImmunoSEQ, AIRR standard, 10x Genomics VDJ). Standardize columns to: cloneId, count, frequency, cdr3aa, cdr3nt, v_gene, j_gene, chain. Define clonotypes using one of three methods:

• cdr3aa: Amino acid CDR3 sequence only
• cdr3nt: Nucleotide CDR3 sequence
• vj_cdr3: V gene + J gene + CDR3aa (most common, recommended)

Aggregate by clonotype, sort by count, assign ranks.

Phase 2: Diversity & Clonality Analysis

Calculate diversity metrics for the repertoire:

• Shannon entropy: Overall diversity (higher = more diverse)
• Simpson index: Probability two random clones are same
• Inverse Simpson: Effective number of clonotypes
• Gini coefficient: Inequality in clonotype distribution
• Clonality: 1 - Pielou's evenness (higher = more clonal)
• Richness: Number of unique clonotypes

Generate rarefaction curves to assess whether sequencing depth is sufficient.

Phase 3: V(D)J Gene Usage Analysis

Analyze V and J gene usage patterns weighted by clonotype count:

• V gene family usage frequencies
• J gene family usage frequencies
• V-J pairing frequencies
• Statistical testing for biased usage (chi-square test vs. uniform expectation)

Phase 4: CDR3 Sequence Analysis

Characterize CDR3 sequences:

• Length distribution: Typical TCR CDR3 = 12-18 aa; BCR CDR3 = 10-20 aa
• Amino acid composition: Weighted by clonotype frequency
• Flag unusual length distributions (may indicate PCR bias)

Phase 5: Clonal Expansion Detection

Identify expanded clonotypes above a frequency threshold (default: 95th percentile). Track clonotypes longitudinally across multiple timepoints to measure persistence, mean/max frequency, and fold changes.

Phase 6: Convergence & Public Clonotypes

• Convergent recombination: Same CDR3 amino acid from different nucleotide sequences (evidence of antigen-driven selection)
• Public clonotypes: Shared across multiple samples/individuals (may indicate common antigen responses)

Phase 7: Epitope Prediction & Specificity

Query epitope databases for known TCR-epitope associations:

• IEDB (iedb_search_tcell_assays): Search T-cell assay records by sequence or MHC class; use iedb_search_epitopes with sequence_contains for motif search
• BVBRC (BVBRC_search_epitopes): Best for organism-based epitope discovery (e.g., taxon_id="2697049" for SARS-CoV-2); returns epitope sequences with T-cell/B-cell assay counts
• VDJdb (manual): https://vdjdb.cdr3.net/search
• PubMed literature (PubMed_search_articles): Search for CDR3 + epitope/antigen/specificity
• IEDB detail tools: iedb_get_epitope_antigens (link epitope→antigen), iedb_get_epitope_mhc (MHC restriction)

Phase 8: Integration with Single-Cell Data

Link TCR/BCR clonotypes to cell phenotypes from paired single-cell RNA-seq:

• Map clonotypes to cell barcodes
• Identify expanded clonotype phenotypes on UMAP
• Analyze clonotype-cluster associations (cross-tabulation)
• Find cluster-specific clonotypes (>80% cells in one cluster)
• Differential gene expression: expanded vs. non-expanded cells

ToolUniverse Tool Integration

Key Tools Used:

• iedb_search_tcell_assays - T-cell assay records (sequence, MHC class filters)
• iedb_search_bcell - B-cell assay records
• iedb_search_epitopes - Epitope motif search via sequence_contains
• BVBRC_search_epitopes - Organism-based epitope discovery (best for pathogen-specific queries)
• NCBI_SRA_search_runs - Find public TCR/BCR-seq datasets (use strategy="AMPLICON")
• ImmPort_search_studies - NIAID immunology studies (vaccine trials, flow cytometry)
• PubMed_search_articles - Literature on TCR/BCR specificity
• UniProt_get_entry_by_accession - Antigen protein information

Integration with Other Skills:

• tooluniverse-single-cell - Single-cell transcriptomics
• tooluniverse-rnaseq-deseq2 - Bulk RNA-seq analysis
• tooluniverse-variant-analysis - Somatic hypermutation analysis (BCR)

Quick Start

from tooluniverse import ToolUniverse

# 1. Load data
tcr_data = load_airr_data("clonotypes.txt", format='mixcr')

# 2. Define clonotypes
clonotypes = define_clonotypes(tcr_data, method='vj_cdr3')

# 3. Calculate diversity
diversity = calculate_diversity(clonotypes['count'])
print(f"Shannon entropy: {diversity['shannon_entropy']:.2f}")

# 4. Detect expanded clones
expansion = detect_expanded_clones(clonotypes)
print(f"Expanded clonotypes: {expansion['n_expanded']}")

# 5. Analyze V(D)J usage
vdj_usage = analyze_vdj_usage(tcr_data)

# 6. Query epitope databases
top_clones = expansion['expanded_clonotypes']['clonotype'].head(10)
epitopes = query_epitope_database(top_clones)

Reasoning Framework for Result Interpretation

Evidence Grading

Interpretation Guidance

• Clonality metrics: Shannon diversity measures overall repertoire complexity (higher = more diverse, typical range 5-12 for healthy blood). Gini coefficient ranges from 0 (perfectly even) to 1 (single dominant clone); values > 0.3 suggest clonal expansion. Clonality (1 - Pielou's evenness) > 0.2 indicates moderate clonal dominance; > 0.5 suggests strong oligoclonal expansion (common in active infection or tumor-infiltrating lymphocytes).
• V(D)J usage significance: Biased V or J gene usage (chi-square p < 0.01 vs expected uniform distribution) may indicate antigen-driven selection. However, baseline V gene usage is not uniform even in healthy repertoires due to genomic proximity and recombination efficiency. Compare against healthy donor reference distributions rather than uniform expectation when possible.
• CDR3 convergence meaning: Convergent recombination (same CDR3 amino acid from different nucleotide sequences) is strong evidence of antigen-driven selection because independent recombination events converged on the same receptor. Public clonotypes (shared across individuals) further strengthen this inference. A convergence ratio > 2 (nucleotide variants per amino acid sequence) for expanded clones is noteworthy.
• Sequencing depth: Rarefaction curves that plateau indicate sufficient depth. If the curve is still rising, richness and diversity estimates are underestimates. Minimum recommended depth: 50,000-100,000 total reads for bulk TCR-seq.
• Longitudinal tracking: Persistent clones across timepoints with stable or increasing frequency indicate antigen-driven maintenance. Transient expansions that disappear may reflect acute responses.

Synthesis Questions

1. Does the observed clonal expansion pattern (Gini coefficient, top-clone frequency) match the expected immune context (e.g., post-vaccination expansion, tumor-infiltrating lymphocyte oligoclonality)?
2. Are convergent CDR3 sequences found across multiple individuals in the cohort, suggesting a public response to a shared antigen?
3. Do expanded clonotypes show biased V gene usage consistent with known antigen-specific repertoire features (e.g., TRBV20-1 enrichment in CMV-specific responses)?
4. Is the sequencing depth sufficient (rarefaction plateau reached) to reliably estimate diversity metrics and detect low-frequency expanded clones?
5. For longitudinal data, do clonal dynamics (expansion, contraction, persistence) correlate with clinical outcomes or treatment response?

References

• Dash P, et al. (2017) Quantifiable predictive features define epitope-specific T cell receptor repertoires. Nature
• Glanville J, et al. (2017) Identifying specificity groups in the T cell receptor repertoire. Nature
• Stubbington MJT, et al. (2016) T cell fate and clonality inference from single-cell transcriptomes. Nature Methods
• Vander Heiden JA, et al. (2014) pRESTO: a toolkit for processing high-throughput sequencing raw reads of lymphocyte receptor repertoires. Bioinformatics

See Also

• ANALYSIS_DETAILS.md - Detailed code snippets for all 8 phases
• USE_CASES.md - Complete use cases (immunotherapy, vaccine, autoimmune, single-cell integration) and best practices