Evidence map›Paper›PMID 16086018›Full record

ArticleNature immunology2005

Function of NKG2D in natural killer cell-mediated rejection of mouse bone marrow grafts.

Kouetsu Ogasawara, Jonathan Benjamin, Rayna Takaki, Joseph H Phillips, Lewis L Lanier

Open access · greenAbstract readComparative Study
In one paragraph

Article in Nature immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
6.0field-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

77 citing papers in PubMed, 170 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. The natural killer cell activating receptor, NKG2D, is critical to antibody-dependent chronic rejection in heart transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Anti-NKG2D mAb: A New Treatment for Crohn's Disease?International journal of molecular sciences · 2017
    Review
  19. Article
  20. Review

17 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

5 authors at 3 institutions in 2 countries.

Kouetsu OgasawaraDepartment of Microbiology & Immunology and the Cancer Research Institute, University of California, San Francisco, California 94143-0414, USA.
Jonathan Benjamin
Rayna Takaki
Joseph H Phillips
Lewis L Lanier
Cancer Research Institute · USUniversity of California, San Francisco · USPalo Alto University · US

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
RAE-1 Family of Proteins in Innate and Adaptive ImmunityR01CA095137 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LANIER, LEWIS LEE · 2003 to 2013
$2.9M
NCI NIH HHS CA95137NCI NIH HHS R01 CA095137NIDDK NIH HHS P30 DK026743NIDDK NIH HHS P30-DK26743
6 · The paper itself

Abstract

Irradiation-resistant natural killer (NK) cells in an F(1) recipient can reject parental bone marrow, and host NK cells can also prevent engraftment of allogeneic bone marrow. We show here that repopulating bone marrow cells in certain mouse strains expressed retinoic acid early inducible 1 proteins, which are ligands for the activating NKG2D NK cell receptor. Treatment with a neutralizing antibody to NKG2D prevented rejection of parental BALB/c bone marrow in (C57BL/6 x BALB/c) F(1) recipients and allowed engraftment of allogeneic BALB.B bone marrow in C57BL/6 recipients. Additionally, bone marrow from C57BL/6 mice transgenic for retinoic acid early inducible 1epsilon was rejected by syngeneic mice but was accepted after treatment with antibody to NKG2D. If other stem cells or tissues upregulate expression of NKG2D ligands after transplantation, NKG2D may contribute to graft rejection in immunocompetent hosts.

Indexed as

Graft RejectionAnimalsAntibodies, MonoclonalBone Marrow CellsBone Marrow TransplantationCarrier ProteinsHistocompatibility Antigens Class IKiller Cells, NaturalLigandsMembrane ProteinsMiceMice, Inbred StrainsMice, KnockoutMice, TransgenicMinor Histocompatibility AntigensNK Cell Lectin-Like Receptor Subfamily KAntibodies, MonoclonalCarrier ProteinsHistocompatibility Antigens Class IKlrk1 protein, mouseLigandsMembrane Proteinsminor H antigen H60Minor Histocompatibility AntigensNK Cell Lectin-Like Receptor Subfamily KRaet1a protein, mouseReceptors, ImmunologicReceptors, Natural Killer CellUL16 binding protein 1, mouse

Identifiers

PMID16086018
PMCPMC1351289
OpenAlexW2061079054

What OpenQuestion holds

Textmetadata
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.