Evidence map›Paper›PMID 22174155›Full record

ArticleBlood2012

Interactions between NKT cells and Tregs are required for tolerance to combined bone marrow and organ transplants.

David Hongo, Xiaobin Tang, Suparna Dutt, Roland G Nador, Samuel Strober

Open access · greenAbstract read
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Unconventional T cells and kidney disease.Nature reviews. Nephrology · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. CD4Frontiers in immunology · 2019
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

David HongoDepartment of Medicine, Division of Immunology and Rheumatology, Stanford University School of Medicine, 296 Campus Drive, Stanford, CA 94305, USA.
Xiaobin Tang
Suparna Dutt
Roland G Nador
Samuel Strober
Stanford University · US

Funding

TUMOR SPECIFIC CYTOTOXIC T-LYMPHOCYTES IN BONE MARROW TRANSPLANTATIONP01CA049605 · NCI · STANFORD UNIVERSITY · PI David B. Miklos · 1989 to 2026
$73.3M
TLI/ATG CONDTIONING: KIDNEY/BLOOD STEM CELL TRANSPLANTSP01HL075462 · NHLBI · STANFORD UNIVERSITY · PI ENGLEMAN, EDGAR G. · 2004 to 2020
$27.9M
DONOR CELL FACILITATION OF TOLERANCER01AI037683 · NIAID · STANFORD UNIVERSITY · PI STROBER, SAMUEL · 1995 to 2011
$3.2M
NCI NIH HHS P01 CA049605NCI NIH HHS P01-CA-49605NHLBI NIH HHS P01 HL075462NHLBI NIH HHS P01-HL-075462NIAID NIH HHS R01 AI037683NIAID NIH HHS R01-AI-037683
6 · The paper itself

Abstract

We used a model of combined bone marrow and heart transplantation, in which tolerance and stable chimerism is induced after conditioning with fractionated irradiation of the lymphoid tissues and anti-T-cell antibodies. Graft acceptance and chimerism required host CD4(+)CD25(+) Treg production of IL-10 that was in-turn enhanced by host invariant natural killer (NK) T-cell production of IL-4. Up-regulation of PD-1 on host Tregs, CD4(+)CD25(-) conventional T (Tcon) cells, and CD8(+) T cells was also enhanced by NKT cell production of IL-4. Up-regulated PD-1 expression on Tregs was linked to IL-10 secretion, on CD8(+) T cells was linked to Tim-3 expression, and on CD4(+) Tcon cells was associated with reduced IFNγ secretion. Changes in the expression of PD-1 were induced by the conditioning regimen, and declined after bone marrow transplantation. In conclusion, NKT cells in this model promoted changes in expression of negative costimulatory receptors and anti-inflammatory cytokines by Tregs and other T-cell subsets in an IL-4-dependent manner that resulted in tolerance to the bone marrow and organ grafts.

Indexed as

AnimalsAntigens, DifferentiationAntilymphocyte SerumBone Marrow TransplantationCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell CommunicationCells, CulturedFemaleFluorescent Antibody TechniqueHeart TransplantationHepatitis A Virus Cellular Receptor 2Immune ToleranceInterferon-gammaInterleukin-10Interleukin-4Antigens, DifferentiationAntilymphocyte SerumHavcr2 protein, mouseHepatitis A Virus Cellular Receptor 2Interferon-gammaInterleukin-10Interleukin-4Pdcd1 protein, mouseProgrammed Cell Death 1 ReceptorReceptors, Virus

Identifiers

PMID22174155
PMCPMC3286219
OpenAlexW1970291262

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.