Evidence map›Paper›PMID 18513355›Full record

ArticleFEMS immunology and medical microbiology2008

Role of two distinct gammadelta T cell subsets during West Nile virus infection.

Thomas Welte, Jacquelyn Lamb, John F Anderson, Willi K Born, Rebecca L O'Brien, Tian Wang

Open access · bronzeAbstract read
In one paragraph

Article in FEMS immunology and medical microbiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. iScience · 2024
    Article
  5. The immune system in neurological diseases: What innate-like T cells have to say.The Journal of allergy and clinical immunology · 2024
    Review
  6. bioRxiv : the preprint server for biology · 2024
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Frontiers in immunology · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

6 authors at 3 institutions in 1 country.

Thomas WelteDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523, USA.
Jacquelyn Lamb
John F Anderson
Willi K Born
Rebecca L O'Brien
Tian Wang
Colorado State University · USNational Jewish Health · USConnecticut Agricultural Experiment Station · US

Funding

The Basis of Functional Variation in Gamma/Delta T cellsR01AI044920 · NIAID · NATIONAL JEWISH HEALTH · PI O'BRIEN, REBECCA L. · 1999 to 2009
$3.0M
AIRWAY FUNCTION--ROLE OF GAMMA DELTA T CELLSR01HL065410 · NHLBI · NATIONAL JEWISH HEALTH · PI BORN, WILLI K · 2000 to 2007
$2.7M
Gammadelta T cell Regulation of Adaptive Immunity in West Nile Virus InfectionR01AI072060 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI WANG, TIAN · 2008 to 2012
$1.9M
Identifying Ligands with Soluble Gamma/Delta TCRsR21AI063400 · NIAID · NATIONAL JEWISH HEALTH · PI O'BRIEN, REBECCA L. · 2005 to 2006
$422k
NHLBI NIH HHS 2R01HL65410NHLBI NIH HHS R01 HL065410NIAID NIH HHS 1R01 AI072060-01A2NIAID NIH HHS 2R01AI44920NIAID NIH HHS R01 AI044920NIAID NIH HHS R01 AI072060NIAID NIH HHS R21 AI063400NIAID NIH HHS R21AI063400
6 · The paper itself

Abstract

gammadelta T cells respond rapidly following West Nile virus (WNV) infection, limiting viremia and invasion of the central nervous system and thereby protecting the host from lethal encephalitis. Here, we investigated the role of two major subpopulations of peripheral gammadelta T cells, Vgamma1(+) and Vgamma4(+) cells, in host immunity against WNV infection. We found initially that aged mice were more susceptible to WNV infection than young mice. Following WNV challenge, Vgamma1(+) cells in young mice expanded significantly whereas Vgamma4(+) cells expanded modestly. In contrast, aged mice exhibited a slower and reduced response of Vgamma1(+) cells but maintained a higher content of Vgamma4(+) cells. Vgamma1(+) cells were the major gammadelta subset producing IFN-gamma during WNV infection. Mice depleted of Vgamma1(+) cells had an enhanced viremia and higher mortality to WNV encephalitis. Vgamma4(+) cells had a higher potential for producing tumor necrosis factor-alpha (TNF-alpha), a cytokine known to be involved in blood-brain barrier compromise and WNV entry into the brain. Depletion of Vgamma4(+) cells reduced TNF-alpha level in the periphery, accompanied by a decreased viral load in the brain and a lower mortality to WN encephalitis. These results suggest that Vgamma1(+) and Vgamma4(+) cells play distinct roles in protection and pathogenesis during WNV infection.

Indexed as

Age FactorsAnimalsInterferon-gammaLymphocyte DepletionMiceMice, Inbred C57BLReceptors, Antigen, T-Cell, gamma-deltaSurvival AnalysisT-Lymphocyte SubsetsTumor Necrosis Factor-alphaViremiaWest Nile FeverWest Nile virusInterferon-gammaReceptors, Antigen, T-Cell, gamma-deltaTumor Necrosis Factor-alpha

Identifiers

PMID18513355
PMCPMC2755494
OpenAlexW2018084083

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.