Evidence map›Paper›PMID 23733329›Full record

ArticleStem cells (Dayton, Ohio)2013

Natural killer cell-activating receptor NKG2D mediates innate immune targeting of allogeneic neural progenitor cell grafts.

Lori K Phillips, Elizabeth A Gould, Harish Babu, Sheri M Krams, Theo D Palmer, Olivia M Martinez

Abstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Maintenance of Hypoimmunogenic FeaturesFrontiers in bioengineering and biotechnology · 2022
    Article
  6. Mouse CD8Cancer immunology, immunotherapy : CII · 2019
    Article
  7. Differential role of natural killer group 2D in recognition and cytotoxicity of hepatocyte-like cells derived from embryonic stem cells and induced pluripotent stem cells.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2019
    Article
  8. Promoting remyelination through cell transplantation therapies in a model of viral-induced neurodegenerative disease.Developmental dynamics : an official publication of the American Association of Anatomists · 2019
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. 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.

Lori K PhillipsProgram in Immunology Stanford University School of Medicine University of Colorado, Boulder, Colorado, USA.
Elizabeth A Gould
Harish Babu
Sheri M Krams
Theo D Palmer
Olivia M Martinez

Funding

Neuroimmune Signaling in Neural TransplantationR01NS076756 · NINDS · STANFORD UNIVERSITY · PI PALMER, THEO D · 2012 to 2016
$3.1M
Inflammatory Modulation of Neural Stem Cell FunctionR01MH071472 · NIMH · STANFORD UNIVERSITY · PI PALMER, THEO D · 2005 to 2009
$1.5M
NIMH NIH HHS R01 MH071472NINDS NIH HHS R01 NS076756
6 · The paper itself

Abstract

Cell replacement therapy holds promise for a number of untreatable neurological or psychiatric diseases but the immunogenicity of cellular grafts remains controversial. Emerging stem cell and reprogramming technologies can be used to generate autologous grafts that minimize immunological concerns but autologous grafts may carry an underlying genetic vulnerability that reduces graft efficacy or survival. Healthy allogeneic grafts are an attractive and commercially scalable alternative if immunological variables can be controlled. Stem cells and immature neural progenitor cells (NPC) do not express major histocompatibility complex (MHC) antigens and can evade adaptive immune surveillance. Nevertheless, in an experimental murine model, allogeneic NPCs do not survive and differentiate as well as syngeneic grafts, even when traditional immunosuppressive treatments are used. In this study, we show that natural killer (NK) cells recognize the lack of self-MHC antigens on NPCs and pose a barrier to NPC transplantation. NK cells readily target both syngeneic and allogeneic NPC, and killing is modulated primarily by NK-inhibiting "self" class I MHC and NK-activating NKG2D-ligand expression. The absence of NKG2D signaling in NK cells significantly improves NPC-derived neuron survival and differentiation. These data illustrate the importance of innate immune mechanisms in graft outcome and the potential value of identifying and targeting NK cell-activating ligands that may be expressed by stem cell derived grafts.

Indexed as

Stem Cell TransplantationAnimalsAntigens, LyCell MovementCytotoxicity, ImmunologicHistocompatibility Antigens Class IImmunity, InnateKiller Cells, NaturalLigandsMiceMice, Inbred C57BLNatural Cytotoxicity Triggering Receptor 1Neural Stem CellsNeuronsNK Cell Lectin-Like Receptor Subfamily KTransplantation, HomologousAntigens, LyHistocompatibility Antigens Class ILigandsNatural Cytotoxicity Triggering Receptor 1Ncr1 protein, mouseNK Cell Lectin-Like Receptor Subfamily KHippocampusLectin-like receptor subfamily KNatural killer cellsNeural stem cellsNKG2DStem cell transplantation

Identifiers

PMID23733329
PMCPMC4199832

What OpenQuestion holds

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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.