Evidence map›Paper›PMID 22739232›Full record

ArticleMucosal immunology2013

IL-22 from conventional NK cells is epithelial regenerative and inflammation protective during influenza infection.

P Kumar, M S Thakar, W Ouyang, S Malarkannan

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

122 citing papers in PubMed, 173 citations in OpenAlex.

  1. Article
  2. Review
  3. Cell-free secretome of CD56Theranostics · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. I don't know about you, but I'm feeling IL-22.Cytokine & growth factor reviews · 2024
    Review
  9. Article
  10. Article
  11. Natural killer cells in the lung: potential role in asthma and virus-induced exacerbation?European respiratory review : an official journal of the European Respiratory Society · 2023
    Review
  12. OMIP-086: Full spectrum flow cytometry for high-dimensional immunophenotyping of mouse innate lymphoid cells.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

62 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

4 authors at 2 institutions in 1 country.

P KumarLaboratory of Molecular Immunology and Immunotherapy, Blood Research Institute, Milwaukee, Wisconsin, USA.
M S Thakar
W Ouyang
S Malarkannan
Versiti Blood Center of Wisconsin · USMedical College of Wisconsin · US

Funding

Molecular Mechanisms of Natural Killer Cell ActivationR01AI064828 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI MALARKANNAN, SUBRAMANIAM · 2006 to 2010
$1.7M
NIAID NIH HHS R01 AI064828PHS HHS R01 A1064828
6 · The paper itself

Abstract

Influenza infection primarily targets the upper respiratory system, leading to a severe destruction of the epithelial cell layer. The role of immune cells in the regeneration of tracheal and bronchial epithelial cells is not well defined. Here, we investigated the production of pro-constructive cytokine, Interleukin-22 (IL-22), in the bronchoalveolar lavage (BAL), trachea, lung tissue, and spleen during influenza infection. We found that conventional natural killer (NK) cells (NCR1(+)NK1.1(+)CD127(-)RORγt(-)) were the predominant IL-22-producers in the BAL, trachea, and lung tissues. Tracheal epithelial cells constitutively expressed high levels of IL-22R and underwent active proliferation in response to IL-22 in the wild-type mice. Infection of IL-22(-/-) mice with influenza virus resulted in a severe impairment in the regeneration of tracheal epithelial cells. In addition, IL-22(-/-) mice continued to lose body weight even after 10 days post infection without any recovery. Tracheal epithelial cell proliferation was significantly reduced in IL-22(-/-) mice during influenza infection. Adoptive transfer of IL-22-sufficient but not IL-22-deficient NK cells into IL-22(-/-) mice restored the tracheal/bronchial epithelial cell regeneration and conferred protection against inflammation. Our findings strongly suggest that conventional NK cells have evolved to both kill virus-infected cells and also to provide vital cytokines for tissue regeneration.

Indexed as

Adoptive TransferAnimalsBronchoalveolar Lavage FluidCell ProliferationEpithelial CellsHumansInflammationInterleukin-22InterleukinsKiller Cells, NaturalLungMiceNatural Cytotoxicity Triggering Receptor 1OrthomyxoviridaeOrthomyxoviridae InfectionsRegenerationInterleukin-22InterleukinsNatural Cytotoxicity Triggering Receptor 1

Identifiers

PMID22739232
PMCPMC3835350
OpenAlexW2017354770

What OpenQuestion holds

Textmetadata
LicenceTDM
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.