Evidence map›Paper›PMID 18802053›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Umbilical cord blood T cells express multiple natural cytotoxicity receptors after IL-15 stimulation, but only NKp30 is functional.

Qin Tang, Bartosz Grzywacz, Hongbo Wang, Nandini Kataria, Qing Cao, John E Wagner, Bruce R Blazar, Jeffrey S Miller, Michael R Verneris

Abstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–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

28 citing papers in PubMed.

  1. Article
  2. NKp30: A Key Membrane Molecule in the Fight Against Cancer and Infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  3. Review
  4. Review
  5. CD4Journal of cancer research and clinical oncology · 2023
    Article
  6. Review
  7. Article
  8. Review
  9. Observational
  10. Article
  11. Article
  12. Review
  13. Article
  14. Distinct human circulating NKp30Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. Innovative Clinical Perspectives for CIK Cells in Cancer Patients.International journal of molecular sciences · 2018
    Review
  16. Review
  17. Review
  18. Article
  19. Enhanced cytotoxic function of natural killer and CD3+CD56+ cells in cord blood after culture.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2015
    Article
  20. 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

9 authors.

Qin TangDepartment of Pediatrics, Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.
Bartosz Grzywacz
Hongbo Wang
Nandini Kataria
Qing Cao
John E Wagner
Bruce R Blazar
Jeffrey S Miller
Michael R Verneris

Funding

Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI J SUNIL RAO · 1995 to 2026
$48.2M
IN VIVO PREVENTION OF MURINE GVHDR01AI034495 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1993 to 2016
$6.2M
GVL TO REDUCE AML RELAPSE AFTER MURINE ALLOGENEIC BMTR01CA072669 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1997 to 2017
$4.9M
NK Cell Differentiation from Stem CellsR01HL055417 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MILLER, JEFFREY S. · 2000 to 2010
$3.2M
NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA65493NCI NIH HHS R01 CA072669NCI NIH HHS R01 CA72669NHLBI NIH HHS R01 HL055417NHLBI NIH HHS R01 HL55417NIAID NIH HHS R01 AI034495NIAID NIH HHS R01 AI34495
6 · The paper itself

Abstract

The natural cytotoxicity receptors (NCRs) NKp30, NKp44, and NKp46 are thought to be NK lineage restricted. Herein we show that IL-15 induces NCR expression on umbilical cord blood (UCB) T cells. NCRs were mainly on CD8(+) and CD56(+) UCB T cells. Only NKp30 was functional as demonstrated by degranulation, IFN-gamma release, redirected killing, and apoptosis. Since NCRs require adaptor proteins for function, the expressions of these adaptors were determined. The adaptors used by NKp30 and NKp46, FcepsilonR1gamma and CD3zeta, were detected in UCB T cells. There was a near absence of DAP12, the adaptor for NKp44, consistent with a hypofunctional state. NKp46 was on significantly fewer UCB T cells, possibly accounting for its lack of function. Adult peripheral blood (PB) T cells showed minimal NCR acquisition after culture with IL-15. Since UCB contains a high frequency of naive T cells, purified naive T cells from adult PB were tested. Although NKp30 was expressed on a small fraction of naive PB T cells, it was nonfunctional. In contrast to UCB, PB T cells lacked FcepsilonR1gamma expression. These results demonstrate differences between UCB and PB T cells regarding NCR expression and function. Such findings challenge the concept that NCRs are NK cell specific.

Indexed as

Cytotoxicity Tests, ImmunologicAdultAnimalsApoptosisCell DegranulationCell Line, TumorCells, CulturedCell SeparationFetal BloodGene Expression RegulationHumansInterferon-gammaInterleukin-15Lymphocyte ActivationMiceNatural Cytotoxicity Triggering Receptor 3Interferon-gammaInterleukin-15Natural Cytotoxicity Triggering Receptor 3NCR3 protein, human

Identifiers

PMID18802053
PMCPMC2614673

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.