Evidence map›Paper›PMID 21067780›Full record

ArticleThe Journal of surgical research2011

Prevention of NKT cell activation accelerates cutaneous wound closure and alters local inflammatory signals.

David F Schneider, Jessica L Palmer, Julia M Tulley, Elizabeth J Kovacs, Richard L Gamelli, Douglas E Faunce

Open access · greenAbstract read
In one paragraph

Article in The Journal of surgical research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Role of NK Cells in Skin Wound Healing of Mice.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Toll-Like Receptor Function in Acute Wounds.Advances in wound care · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Chemokines in health and disease.Experimental cell research · 2011
    Review
  16. 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

6 authors at 1 institution in 1 country.

David F SchneiderDepartment of Surgery, Burn and Shock Trauma Institute, Loyola University Medical Center, Maywood, IL, USA.
Jessica L Palmer
Julia M Tulley
Elizabeth J Kovacs
Richard L Gamelli
Douglas E Faunce
Loyola University Medical Center · US

Funding

TRAINING IN TRAUMA AND BURN RESEARCHT32GM008750 · NIGMS · LOYOLA UNIVERSITY CHICAGO · PI CHOUDHRY, MASHKOOR A, GONZALEZ, RICHARD PAUL · 2000 to 2023
$2.9M
Natural Killer T cells and the immune response to injuryR01AI056108 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KOVACS, ELIZABETH J. · 2004 to 2008
$1.5M
Natural Killer T Cell Modulation of Cutaneous Wound HealingR21AI073987 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KOVACS, ELIZABETH J. · 2009 to 2010
$411k
NIAID NIH HHS R01 AI056108NIAID NIH HHS R01 AI56108NIAID NIH HHS R21 AI073987NIGMS NIH HHS T32 GM008750NIGMS NIH HHS T32 GM08750
6 · The paper itself

Abstract

We previously reported that in the absence of NKT cells, wound closure was accelerated in a murine excisional punch wound model. Here, we explored whether purposefully inhibiting NKT cell activation had similar effects on wound closure and the dermal inflammatory response to injury. We found that prevention of NKT cell activation accelerated wound closure in a dose-responsive manner. If anti-CD1d was administered before wounding, NKT cell infiltration into cutaneous wounds was diminished without quantitative changes in cellular infiltrates. Furthermore, prevention of NKT cell activation transiently enhanced the local production of a subset of chemokines, including MIP-2, MCP-1, MIP-1α, and MIP-1β, and altered the relative expression of CD69 and CXCR2 on the surface of both circulating and wound NKT cells. Taken together, these findings suggest that wounding activates NKT cells via CD1d presentation of glycolipid antigen and help further define a role for NKT cells in the regulation of wound inflammation and closure. Many soluble factors have been targeted as potential wound healing therapies, but their clinical success has been limited. Given our findings, the NKT cell may be an attractive target for wound healing therapies.

Indexed as

AnimalsAntibodiesChemokinesDermatitisFlow CytometryLymphocyte ActivationMaleMiceMice, Inbred BALB CNatural Killer T-CellsReceptors, Interleukin-8BSignal TransductionSkinSpleenWound HealingAntibodiesChemokinesReceptors, Interleukin-8B

Identifiers

PMID21067780
PMCPMC3324976
OpenAlexW2124952535

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.