Evidence map›Paper›PMID 27269786›Full record

ArticleVeterinary immunology and immunopathology2016

NK cells are intrinsically functional in pigs with Severe Combined Immunodeficiency (SCID) caused by spontaneous mutations in the Artemis gene.

Ellis J Powell, Joan E Cunnick, Susan M Knetter, Crystal L Loving, Emily H Waide, Jack C M Dekkers, Christopher K Tuggle

Abstract read
In one paragraph

Article in Veterinary immunology and immunopathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Pigs: Large Animal Preclinical Cancer Models.World journal of oncology · 2024
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. CD3εFrontiers in immunology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. SCID pigs: An emerging large animal NK model.Journal of rare diseases research & treatment · 2017
    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

7 authors at 2 institutions in 1 country.

Ellis J PowellIowa State University, Department of Animal Science, Ames, IA, USA.
Joan E CunnickIowa State University, Department of Animal Science, Ames, IA, USA.
Susan M KnetterIowa State University, Department of Animal Science, Ames, IA, USA.
Crystal L LovingUSDA-ARS-National Animal Disease Center, Food Safety and Enteric Pathogens Research Unit, USA.
Emily H WaideIowa State University, Department of Animal Science, Ames, IA, USA.
Jack C M DekkersIowa State University, Department of Animal Science, Ames, IA, USA.
Christopher K TuggleIowa State University, Department of Animal Science, Ames, IA, USA. Electronic address: cktuggle@iastate.edu.
Iowa State University · USNational Animal Disease Center · US

Funding

Expanding the Utility of Severe Combined Immuno-Deficient (SCID) Pig ModelsR24OD019813 · OD · IOWA STATE UNIVERSITY · PI TUGGLE, CHRISTOPHER · 2015 to 2019
$2.7M
NIH HHS R24 OD019813
6 · The paper itself

Abstract

We have identified Severe Combined Immunodeficiency (SCID) in a line of Yorkshire pigs at Iowa State University. These SCID pigs lack B-cells and T-cells, but possess Natural Killer (NK) cells. This SCID phenotype is caused by recessive mutations in the Artemis gene. Interestingly, two human tumor cell lines, PANC-1 and A375-SM, survived after injection into these SCID pigs, but, as we demonstrate here, these cells, as well as K562 tumor cells, can be lysed in vitro by NK cells from SCID and non-SCID pigs. NK cells from both SCID and non-SCID pigs required activation in vitro with either recombinant human IL-2 or the combination of recombinant porcine IL-12 and IL-18 to kill tumor targets. We also showed that SCID NK cells could be activated to produce perforin, and perforin production was greatly enhanced in NK cells from both SCID and non-SCID pigs after IL-2 cytokine treatment. While CD16+, CD172- NK cells constituted an average of only 4% in non-SCID pigs, NK cells averaged 27% of the peripheral blood mononuclear cell population in SCID pigs. We found no significant differences in killing activity per NK cell between SCID and non-SCID pigs. We conclude that survival of human cancer cells in these SCID pigs is not due to an intrinsic defect in NK cell killing ability.

Indexed as

AnimalsCell Line, TumorCytotoxicity, ImmunologicEndonucleasesFemaleGenes, RecessiveHumansK562 CellsKiller Cells, NaturalLymphocyte ActivationMaleMutationNeoplasm TransplantationSevere Combined ImmunodeficiencySus scrofaSwineEndonucleasesArtemisInnate immunityNatural killerNK cellsPerforinPigSCID

Identifiers

PMID27269786
PMCPMC5130348
OpenAlexW2340604099

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.