Evidence map›Paper›PMID 26125037›Full record

ArticleAnnals of clinical and translational neurology2015

Expanded CD8 T-cell sharing between periphery and CNS in multiple sclerosis.

Marion Salou, Alexandra Garcia, Laure Michel, Anne Gainche-Salmon, Delphine Loussouarn, Bryan Nicol, Flora Guillot, Philippe Hulin, Steven Nedellec, Daniel Baron and 6 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

71 citing papers in PubMed, 104 citations in OpenAlex.

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  18. Patients With Severe Multiple Sclerosis Exhibit Functionally Altered CD8Neurology(R) neuroimmunology & neuroinflammation · 2022
    Article
  19. CD8Molecular neurodegeneration · 2022
    Article
  20. Article

11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Marion SalouINSERM, UMR 1064 Nantes, F-44093, France ; Medicine Department, Nantes University Nantes, F-44035, France.
Alexandra GarciaINSERM, UMR 1064 Nantes, F-44093, France ; Nantes Hospital, ITUN Nantes, F-44093, France.
Laure MichelINSERM, UMR 1064 Nantes, F-44093, France ; Neurology Department, Nantes Hospital Nantes, F-44093, France.
Anne Gainche-SalmonINSERM, UMR 1064 Nantes, F-44093, France.
Delphine LoussouarnPathology Department, Nantes Hospital Nantes, F-44093, France.
Bryan NicolINSERM, UMR 1064 Nantes, F-44093, France ; Medicine Department, Nantes University Nantes, F-44035, France.
Flora GuillotINSERM, UMR 1064 Nantes, F-44093, France ; Medicine Department, Nantes University Nantes, F-44035, France.
Philippe HulinSFR François Bonamy, Cellular and Tissue Imaging Core Facility (MicroPICell) Nantes, F-44093, France.
Steven NedellecSFR François Bonamy, Cellular and Tissue Imaging Core Facility (MicroPICell) Nantes, F-44093, France.
Daniel BaronINSERM, UMR 1064 Nantes, F-44093, France ; Medicine Department, Nantes University Nantes, F-44035, France ; Nantes Hospital, ITUN Nantes, F-44093, France.
Gérard RamsteinLINA UMR6241, Nantes University Nantes, F-44093, France.
Jean-Paul SoulillouINSERM, UMR 1064 Nantes, F-44093, France.
Sophie BrouardINSERM, UMR 1064 Nantes, F-44093, France ; Nantes Hospital, ITUN Nantes, F-44093, France.
Arnaud B NicotINSERM, UMR 1064 Nantes, F-44093, France ; Medicine Department, Nantes University Nantes, F-44035, France ; Nantes Hospital, ITUN Nantes, F-44093, France.
Nicolas DegauqueINSERM, UMR 1064 Nantes, F-44093, France ; Nantes Hospital, ITUN Nantes, F-44093, France.
David A LaplaudINSERM, UMR 1064 Nantes, F-44093, France ; Neurology Department, Nantes Hospital Nantes, F-44093, France ; INSERM 004, Centre d'Investigation Clinique Nantes, F-44093, France.
Inserm · FRInstitut de Transplantation Urologie en Nephrologie · FRNantes Université · FRCentre d'Investigation Clinique de Nantes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn multiple sclerosis (MS), central nervous system (CNS), cerebrospinal fluid (CSF), and blood display TCR clonal expansions of CD8(+) T cells. These clones have been assumed - but never demonstrated - to be similar in the three compartments. Addressing this key question is essential to infer the implication of peripheral clonally expanded CD8(+) T cells in the disease.

methodsFor the first time, TCR Vβ repertoire from paired blood (purified CD8(+) and CD4(+) T cells), CSF and CNS (22 lesions, various inflammatory and demyelination statuses) samples from three MS patients was studied using complementary determining region 3 (CDR3) spectratyping and high-throughput sequencing. In parallel, blood and CNS clonally expanded CD8(+) T cells were characterized by fluorescent staining.

resultsTCR Vβ repertoire analysis revealed strong sharing of predominant T-cell clones between CNS lesions, CSF, and blood CD8(+) T cells. In parallel, we showed that blood oligoclonal CD8(+) T cells exhibit characteristics of pathogenic cells, as they displayed a bias toward a memory phenotype in MS patients, with increased expression of CCR5, CD11a and Granzyme B (GZM-B) compared to non oligoclonal counterparts. CNS-infiltrating T cells were mainly CD8 expressing CD11a and GZM-B.

interpretationThis study highlights the predominant implication of CD8(+) T cells in MS pathophysiology and demonstrates that potentially aggressive CD8(+) T cells can be easily identified and characterized from blood and CSF samples.

Identifiers

PMID26125037
PMCPMC4479522
OpenAlexW2015437828

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.