CD8+ T cells with characteristic T cell receptor beta motif are detected in blood and expanded in synovial fluid of ankylosing spondylitis patients
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
29481668
DOI
10.1093/rheumatology/kex517
PII: 4903020
Knihovny.cz E-resources
- MeSH
- Spondylitis, Ankylosing genetics immunology metabolism MeSH
- CD8-Positive T-Lymphocytes immunology MeSH
- DNA genetics MeSH
- POU Domain Factors genetics metabolism MeSH
- Humans MeSH
- Polymerase Chain Reaction MeSH
- Prohibitins MeSH
- Synovial Fluid immunology metabolism MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA MeSH
- POU Domain Factors MeSH
- PHB2 protein, human MeSH Browser
- POU6F1 protein, human MeSH Browser
- Prohibitins MeSH
OBJECTIVE: The risk of AS is associated with genomic variants related to antigen presentation and specific cytokine signalling pathways, suggesting the involvement of cellular immunity in disease initiation/progression. The aim of the present study was to explore the repertoire of TCR sequences in healthy donors and AS patients to uncover AS-linked TCR variants. METHODS: Using quantitative molecular-barcoded 5'-RACE, we performed deep TCR β repertoire profiling of peripheral blood (PB) and SF samples for 25 AS patients and 108 healthy donors. AS-linked TCR variants were identified using a new computational approach that relies on a probabilistic model of the VDJ rearrangement process. RESULTS: Using the donor-agnostic probabilistic model, we reveal a TCR β motif characteristic for PB of AS patients, represented by eight highly homologous amino acid sequence variants. Some of these variants were previously reported in SF and PB of patients with ReA and in PB of AS patients. We demonstrate that identified AS-linked clones have a CD8+ phenotype, present at relatively low frequencies in PB, and are significantly enriched in matched SF samples of AS patients. CONCLUSION: Our results suggest the involvement of a particular antigen-specific subset of CD8+ T cells in AS pathogenesis, confirming and expanding earlier findings. The high similarity of the clonotypes with the ones found in ReA implies common mechanisms for the initiation of the diseases.
5 A Nasonova Research Institute of Rheumatology Moscow Russia
Adaptive Immunity Group Central European Institute of Technology Brno Czech Republic
Biological Department Lomonosov Moscow State University Moscow Russia
City Clinical Hospital 1 Pirogov Russian National Research Medical University Moscow Russia
Gynecology and Perinatology Kulakov Research Center for Obstetrics Moscow Russia
References provided by Crossref.org
Targeted depletion of TRBV9+ T cells as immunotherapy in a patient with ankylosing spondylitis
Detecting T cell receptors involved in immune responses from single repertoire snapshots