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Broader Epstein–Barr virus–specific T cell receptor repertoire in patients with multiple sclerosis

https://doi.org/10.1084/jem.20220650

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Copy number variations across the blood–brain barrier in multiple sclerosis

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Pathogenic CD8+ T cells in multiple sclerosis

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Primary infection with the Epstein‐Barr virus and risk of multiple sclerosis

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High‐throughput sequencing of TCR repertoires in multiple sclerosis reveals intrathecal enrichment of EBV‐reactive CD8+ T cells

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Diagnosis of inflammatory demyelination in biopsy specimens: a practical approach

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Human Tissue-Resident Memory T Cells Are Defined by Core Transcriptional and Functional Signatures in Lymphoid and Mucosal Sites

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T Cell Repertoire Dynamics during Pregnancy in Multiple Sclerosis

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Highly multiplexed immune repertoire sequencing links multiple lymphocyte classes with severity of response to COVID-19

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Understanding Subset Diversity in T Cell Memory

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Epstein–Barr Virus in Multiple Sclerosis: Theory and Emerging Immunotherapies

inferredcites →https://doi.org/10.1016/j.molmed.2021.01.004openalex-snapshot

Epstein–Barr Virus in Multiple Sclerosis: Theory and Emerging Immunotherapies

inferredcites →https://doi.org/10.1016/s1474-4422(22)00086-2openalex-snapshot

Epstein-Barr virus and multiple sclerosis: supporting causality

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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

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inferredcites →https://doi.org/10.1038/ni.3031openalex-snapshot

Molecular regulation of effector and memory T cell differentiation

inferredcites →https://doi.org/10.1038/s41586-022-04419-4openalex-snapshot

Twin study reveals non-heritable immune perturbations in multiple sclerosis

inferredcites →https://doi.org/10.1038/s41586-022-04432-7openalex-snapshot

Clonally expanded B cells in multiple sclerosis bind EBV EBNA1 and GlialCAM

inferredcites →https://doi.org/10.1073/pnas.2003339117openalex-snapshot

Immune Signatures of Prodromal Multiple Sclerosis in Monozygotic Twins

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α4β1Integrin-dependent Cell Adhesion Is Regulated by a Low Affinity Receptor Pool That Is Conformationally Responsive to Ligand

inferredcites →https://doi.org/10.1084/jem.20072397openalex-snapshot

EBNA1-specific T cells from patients with multiple sclerosis cross react with myelin antigens and co-produce IFN-γ and IL-2

inferredcites →https://doi.org/10.1093/brain/awaa117openalex-snapshot

Tissue-resident memory T cells invade the brain parenchyma in multiple sclerosis white matter lesions

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Classification of neurological diseases using multi-dimensional CSF analysis

inferredcites →https://doi.org/10.1093/brain/awl067openalex-snapshot

Increased frequency and broadened specificity of latent EBV nuclear antigen-1-specific T cells in multiple sclerosis

inferredcites →https://doi.org/10.1093/brain/awr197openalex-snapshot

Epstein-Barr virus in the multiple sclerosis brain: a controversial issue--report on a focused workshop held in the Centre for Brain Research of the Medical University of Vienna, Austria

inferredcites →https://doi.org/10.1093/brain/awy151openalex-snapshot

The compartmentalized inflammatory response in the multiple sclerosis brain is composed of tissue-resident CD8+ T lymphocytes and B cells

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The Immune Epitope Database (IEDB): 2018 update

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VDJdb in 2019: database extension, new analysis infrastructure and a T-cell receptor motif compendium

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CNS inflammation after natalizumab therapy for multiple sclerosis: A retrospective histopathological and CSF cohort study

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Programmed death 1 is highly expressed on CD 8+ CD 57+ T cells in patients with stable multiple sclerosis and inhibits their cytotoxic response to Epstein–Barr virus

inferredcites →https://doi.org/10.1126/science.abj8222openalex-snapshot

Longitudinal analysis reveals high prevalence of Epstein-Barr virus associated with multiple sclerosis

inferredcites →https://doi.org/10.1126/sciimmunol.abb8786openalex-snapshot

Transcriptomic and clonal characterization of T cells in the human central nervous system

inferredcites →https://doi.org/10.1128/jvi.00980-19openalex-snapshot

Epstein-Barr Virus-Specific CD8 T Cells Selectively Infiltrate the Brain in Multiple Sclerosis and Interact Locally with Virus-Infected Cells: Clue for a Virus-Driven Immunopathological Mechanism

inferredcites →https://doi.org/10.1136/jclinpath-2019-205822openalex-snapshot

Epstein-Barr virus (EBV) reactivation and therapeutic inhibitors

inferredcites →https://doi.org/10.1136/jnnp-2020-322941openalex-snapshot

Complete Epstein-Barr virus seropositivity in a large cohort of patients with early multiple sclerosis

inferredcites →https://doi.org/10.1136/jnnp.2008.161018openalex-snapshot

Decreased T cell reactivity to Epstein-Barr virus infected lymphoblastoid cell lines in multiple sclerosis

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Modulating Innate and Adaptive Immunity by (R)-Roscovitine: Potential Therapeutic Opportunity in Cystic Fibrosis

inferredcites →https://doi.org/10.1177/1352458515588581openalex-snapshot

Intrathecal CD8 T-cells of multiple sclerosis patients recognize lytic Epstein-Barr virus proteins

inferredcites →https://doi.org/10.1177/1352458520969145openalex-snapshot

BEST-MS: A prospective head-to-head comparative study of natalizumab and fingolimod in active relapsing MS

inferredcites →https://doi.org/10.1177/1352458520970103openalex-snapshot

High anti-JCPyV serum titers coincide with high CSF cell counts in RRMS patients

inferredcites →https://doi.org/10.1182/blood-2009-04-217604openalex-snapshot

Comprehensive assessment of T-cell receptor β-chain diversity in αβ T cells

inferredcites →https://doi.org/10.1182/blood.2020009482openalex-snapshot

CD27 is required for protective lytic EBV antigen–specific CD8+ T-cell expansion

inferredcites →https://doi.org/10.1212/nxi.0000000000000466openalex-snapshot

Molecular signature of Epstein-Barr virus infection in MS brain lesions

inferredcites →https://doi.org/10.1371/journal.ppat.1003220openalex-snapshot

Increased CD8+ T Cell Response to Epstein-Barr Virus Lytic Antigens in the Active Phase of Multiple Sclerosis

inferredcites →https://doi.org/10.18637/jss.v039.i05openalex-snapshot

Regularization Paths for Cox's Proportional Hazards Model via Coordinate Descent

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The stringdist Package for Approximate String Matching

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inferredcites →https://doi.org/10.4049/jimmunol.202.supp.131.4openalex-snapshot

Scalable and comprehensive characterization of antigen-specific CD8 T cells using multi-omics single cell analysis

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Human T cell receptor occurrence patterns encode immune history, genetic background, and receptor specificity

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Humoral response to Epstein-Barr virus in patients with multiple sclerosis treated with B cell depletion therapy

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Ocrelizumab B cell depletion has no effect on HERV RNA expression in PBMC in MS patients

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CD4 T cells restricted to DRB1*15:01 recognize two Epstein–Barr virus glycoproteins capable of intracellular antigen presentation

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