Evidence map›Paper›PMID 22916008›Full record

ReviewPLoS pathogens2012

Invariant NKT cells: regulation and function during viral infection.

Jennifer A Juno, Yoav Keynan, Keith R Fowke

Open access · goldAbstract readReview
In one paragraph

Review in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

85 citing papers in PubMed, 149 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. METTL14-dependent mCell reports · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
  15. Review
  16. Review
  17. Review
  18. Ceramide and Related Molecules in Viral Infections.International journal of molecular sciences · 2021
    Review
  19. Activation ofFrontiers in immunology · 2021
    Article
  20. Review

25 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

3 authors at 2 institutions in 2 countries.

Jennifer A JunoDepartment of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Yoav Keynan
Keith R Fowke
University of Manitoba · CAUniversity of Nairobi · KE

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Natural killer T cells (NKT cells) represent a subset of T lymphocytes that express natural killer (NK) cell surface markers. A subset of NKT cells, termed invariant NKT cells (iNKT), express a highly restricted T cell receptor (TCR) and respond to CD1d-restricted lipid ligands. iNKT cells are now appreciated to play an important role in linking innate and adaptive immune responses and have been implicated in infectious disease, allergy, asthma, autoimmunity, and tumor surveillance. Advances in iNKT identification and purification have allowed for the detailed study of iNKT activity in both humans and mice during a variety of chronic and acute infections. Comparison of iNKT function between non-pathogenic simian immunodeficiency virus (SIV) infection models and chronic HIV-infected patients implies a role for iNKT activity in controlling immune activation. In vitro studies of influenza infection have revealed novel effector functions of iNKT cells including IL-22 production and modulation of myeloid-derived suppressor cells, but ex vivo characterization of human iNKT cells during influenza infection are lacking. Similarly, as recent evidence suggests iNKT involvement in dengue virus pathogenesis, iNKT cells may modulate responses to a number of emerging pathogens. This Review will summarize current knowledge of iNKT involvement in responses to viral infections in both human and mouse models and will identify critical gaps in knowledge and opportunities for future study. We will also highlight recent efforts to harness iNKT ligands as vaccine adjuvants capable of improving vaccination-induced cellular immune responses.

Indexed as

Immunity, CellularImmunity, InnateAcute DiseaseAnimalsAntigens, CD1dChronic DiseaseInterleukin-22InterleukinsLipidsMiceNatural Killer T-CellsVaccinationViral VaccinesVirus DiseasesAntigens, CD1dCD1D protein, humanInterleukin-22InterleukinsLipidsViral Vaccines

Identifiers

PMID22916008
PMCPMC3420949
OpenAlexW2075364390

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.