Literature DB >> 33616082

Immunopathogenic CSF TCR repertoire signatures in virus-associated neurologic disease.

Satoshi Nozuma1, Yoshimi Enose-Akahata1, Kory R Johnson2, Maria Chiara Monaco1, Nyater Ngouth1, Abdel Elkahloun3, Joan Ohayon4, Jun Zhu5, Steven Jacobson1.   

Abstract

In this study, we examined and characterized disease-specific TCR signatures in cerebrospinal fluid (CSF) of patients with HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). TCR β libraries using unique molecular identifier-based methodologies were sequenced in paired peripheral blood mononuclear cells (PBMCs) and CSF cells from HAM/TSP patients and normal healthy donors (NDs). The sequence analysis demonstrated that TCR β repertoires in CSF of HAM/TSP patients were highly expanded and contained both TCR clonotypes shared with PBMCs and uniquely enriched within the CSF. In addition, we analyzed TCR β repertoires of highly expanded and potentially immunopathologic HTLV-1 Tax11-19-specific CD8+ T cells from PBMCs of HLA-A*0201+ HAM/TSP and identified a conserved motif (PGLAG) in the CDR3 region. Importantly, TCR β clonotypes of expanded clones in HTLV-1 Tax11-19-specific CD8+ T cells were also expanded and enriched in the CSF of the same patient. These results suggest that exploring TCR repertoires of CSF and antigen-specific T cells may provide a TCR repertoire signature in virus-associated neurologic disorders.

Entities:  

Keywords:  Immunology; Infectious disease; Neurological disorders; T cell receptor

Mesh:

Substances:

Year:  2021        PMID: 33616082      PMCID: PMC7934934          DOI: 10.1172/jci.insight.144869

Source DB:  PubMed          Journal:  JCI Insight        ISSN: 2379-3708


  43 in total

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4.  Human T cell leukemia virus Type I (HTLV-I) infection induces greater expansions of CD8 T lymphocytes in persons with HTLV-I-associated myelopathy/tropical spastic paraparesis than in asymptomatic carriers.

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Journal:  Sci Immunol       Date:  2018-02-02

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Review 9.  An overview of immunoinformatics approaches and databases linking T cell receptor repertoires to their antigen specificity.

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