Evidence map›Paper›PMID 24282598›Full record

ArticlePloS one2013

CD4+NKG2D+ T cells exhibit enhanced migratory and encephalitogenic properties in neuroinflammation.

Tobias Ruck, Stefan Bittner, Catharina C Gross, Johanna Breuer, Stefanie Albrecht, Sabrina Korr, Kerstin Göbel, Susann Pankratz, Christian M Henschel, Nicholas Schwab and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
1.3field-weighted citation impact, top 21% 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, 39 citations in OpenAlex.

  1. Article
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  6. Innate acting memory Th1 cells modulate heterologous diseases.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  13. KCell research · 2022
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  15. Article
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  17. Article
  18. Review
  19. Article
  20. TGF-β1 expression in regulatory NK1.1American journal of cancer research · 2018
    Article
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

15 authors at 4 institutions in 3 countries.

Tobias RuckDepartment of Neurology, University of Münster, Münster, Germany.
Stefan Bittner
Catharina C Gross
Johanna Breuer
Stefanie Albrecht
Sabrina Korr
Kerstin Göbel
Susann Pankratz
Christian M Henschel
Nicholas Schwab
Ori Staszewski
Marco Prinz
Tanja Kuhlmann
Sven G Meuth
Heinz Wiendl
University of Münster · DEMacalester College · USUniversity of Freiburg · DEYork Minster · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Migration of encephalitogenic CD4(+) T lymphocytes across the blood-brain barrier is an essential step in the pathogenesis of multiple sclerosis (MS). We here demonstrate that expression of the co-stimulatory receptor NKG2D defines a subpopulation of CD4(+) T cells with elevated levels of markers for migration, activation, and cytolytic capacity especially when derived from MS patients. Furthermore, CD4(+)NKG2D(+) cells produce high levels of proinflammatory IFN-γ and IL-17 upon stimulation. NKG2D promotes the capacity of CD4(+)NKG2D(+) cells to migrate across endothelial cells in an in vitro model of the blood-brain barrier. CD4(+)NKG2D(+) T cells are enriched in the cerebrospinal fluid of MS patients, and a significant number of CD4(+) T cells in MS lesions coexpress NKG2D. We further elucidated the role of CD4(+)NKG2D(+) T cells in the mouse system. NKG2D blockade restricted central nervous system migration of T lymphocytes in vivo, leading to a significant decrease in the clinical and pathologic severity of experimental autoimmune encephalomyelitis, an animal model of MS. Blockade of NKG2D reduced killing of cultivated mouse oligodendrocytes by activated CD4(+) T cells. Taken together, we identify CD4(+)NKG2D(+) cells as a subpopulation of T helper cells with enhanced migratory, encephalitogenic and cytotoxic properties involved in inflammatory CNS lesion development.

Indexed as

Chemotaxis, LeukocyteBlood-Brain BarrierCD4-Positive T-LymphocytesEncephalomyelitis, Autoimmune, ExperimentalHumansMultiple SclerosisNK Cell Lectin-Like Receptor Subfamily KSignal TransductionKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID24282598
PMCPMC3839937
OpenAlexW1990869196

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.