Evidence map›Paper›PMID 20813972›Full record

ArticleThe American journal of pathology2010

Rapid formation of extended processes and engagement of Theiler's virus-infected neurons by CNS-infiltrating CD8 T cells.

Jeremiah R McDole, Steve C Danzer, Raymund Y K Pun, Yi Chen, Holly L Johnson, Istvan Pirko, Aaron J Johnson

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Getting on your last nerve: IFNs and resistance to infection.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Dissection of Neurotropic Theiler's Murine Encephalomyelitis Virus Induced Brain Atrophy in Single MHC Class I Mice of C57BL/6 Background.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Cytotoxic CD8Brain pathology (Zurich, Switzerland) · 2018
    Article
  15. Article
  16. Review
  17. Brain atrophy in picornavirus-infected FVB mice is dependent on the H-2DFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  18. Article
  19. Article
  20. Review
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

7 authors at 5 institutions in 2 countries.

Jeremiah R McDoleDepartments of Neurology,University of Cincinnati College of Medicine , Cincinnati, OH 45267, USA.
Steve C Danzer
Raymund Y K Pun
Yi Chen
Holly L Johnson
Istvan Pirko
Aaron J Johnson
Institut des Sciences Cognitives Marc Jeannerod · FRUniversity of Cincinnati · USCenter for Neurosciences · USSociety for Neuroscience · USUniversity of Cincinnati Medical Center · US

Funding

CD 8 T Cell Mediated Disruption of Blood Brain Tight JunctionR01NS060881 · NINDS · UNIVERSITY OF CINCINNATI · PI JOHNSON, AARON J · 2009 to 2013
$1.7M
CD8+ T cells in formation of T1 black holes in animal model of multiple sclerosisR01NS058698 · NINDS · UNIVERSITY OF CINCINNATI · PI PIRKO, ISTVAN · 2008 to 2011
$1.2M
NINDS NIH HHS NS058698NINDS NIH HHS NS060881NINDS NIH HHS R01 NS058698NINDS NIH HHS R01 NS060881
6 · The paper itself

Abstract

A fundamental question in neuroimmunology is the extent to which CD8 T cells actively engage virus-infected neurons. In the Theiler's murine encephalomyelitis virus (TMEV) model of multiple sclerosis, an effective central nervous system (CNS)-infiltrating antiviral CD8 T cell response offers protection from this demyelinating disease. However, the specific CNS cell types engaged by these protective CD8 T cells in TMEV-resistant strains remains unknown. We used confocal microscopy to visualize the morphology, migration, and specific cellular interactions between adoptively transferred CD8 T cells and specific CNS cell types. Adoptively transferred GFP+ CD8+ splenocytes migrated to the brain and became 93% specific for the immunodominant virus epitope D(b):VP2(121-130). These CD8 T cells also polarized T cell receptor, CD8 protein, and granzyme B toward target neurons. Furthermore, we observed CD8 T cells forming cytoplasmic processes up to 45 μm in length. Using live tissue imaging, we determined that these T cell-extended processes (TCEPs) could be rapidly formed and were associated with migratory behavior through CNS tissues. These studies provide evidence that antiviral CD8 T cells have the capacity to engage virus-infected neurons in vivo and are the first to document and measure the rapid formation of TCEPs on these brain-infiltrating lymphocytes using live tissue imaging.

Indexed as

Adoptive TransferAnimalsBrainCardiovirus InfectionsCD8-Positive T-LymphocytesCentral Nervous SystemCentral Nervous System Viral DiseasesEpitopes, T-LymphocyteFemaleImmunoenzyme TechniquesLymphocyte ActivationMiceMice, Inbred C57BLNeuronsTheilovirusEpitopes, T-Lymphocyte

Identifiers

PMID20813972
PMCPMC2947278
OpenAlexW2167414475

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.