Evidence map›Paper›PMID 19657090›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Tissue-specific homing and expansion of donor NK cells in allogeneic bone marrow transplantation.

Janelle A Olson, Robert Zeiser, Andreas Beilhack, Joshua J Goldman, Robert S Negrin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

29 citing papers in PubMed, 52 citations in OpenAlex.

  1. Trial
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  9. Combining Immunocytokine andFrontiers in immunology · 2021
    Article
  10. Article
  11. Lineage specification in innate lymphocytes.Cytokine & growth factor reviews · 2018
    Review
  12. Article
  13. Review
  14. Article
  15. Design and Synthesis of an Alkynyl Luciferin Analogue for Bioluminescence Imaging.Chemistry (Weinheim an der Bergstrasse, Germany) · 2016
    Article
  16. Article
  17. Article
  18. Review
  19. 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

5 authors at 3 institutions in 2 countries.

Janelle A OlsonDepartment of Medicine, Division of Blood and Marrow Transplantation, Stanford University, Stanford, CA 94305, USA.
Robert Zeiser
Andreas Beilhack
Joshua J Goldman
Robert S Negrin
Stanford Blood Center · USUniversity of Freiburg · DEUniversity of Würzburg · DE

Funding

TUMOR SPECIFIC CYTOTOXIC T-LYMPHOCYTES IN BONE MARROW TRANSPLANTATIONP01CA049605 · NCI · STANFORD UNIVERSITY · PI David B. Miklos · 1989 to 2026
$73.3M
MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
NK Cells in GVHD and GVTR01CA125276 · NCI · STANFORD UNIVERSITY · PI NEGRIN, ROBERT S · 2008 to 2012
$1.5M
NCI NIH HHS 1 R01 CA125276NCI NIH HHS P01 CA049605NCI NIH HHS R01 CA125276NIAID NIH HHS T32 AI007290
6 · The paper itself

Abstract

NK cells have potential therapeutic impact in suppressing graft-versus-host disease (GVHD) and enhancing antitumor effects as a cellular therapy for hematologic malignancies. However, few studies have addressed the trafficking and in vivo behavior of NK cells in murine models of bone marrow transplantation (BMT). We investigated NK cell trafficking and survival following allogeneic and syngeneic BMT using a novel bioluminescence-based imaging strategy. Transplantation of luciferase-expressing NK cells revealed CD62L-mediated trafficking to lymphoid organs and trafficking to GVHD target tissues, as evidenced by in vivo and ex vivo bioluminescence imaging. The NK cells persisted for approximately 4 wk after transplantation in allogeneic recipients, but were not detectable in syngeneic recipients. CFSE-labeling studies showed extensive NK cell proliferation in vivo. Transplanted NK cells up-regulated molecules necessary for homing to the lymph nodes, gastrointestinal tract, and skin, yet did not cause clinical GVHD. This expansion and tissue-specific homing was not solely due to the conditioning regimen, as NK cells proliferated and reached lymphoid and GVHD target tissue in unconditioned allogeneic RAG2(-/-) gamma-chain(-/-) recipients. IL-2 enhanced expansion and antitumor activity of NK cells. These results provide significant insight into the behavior and potential therapeutic impact of NK cells in BMT.

Indexed as

Cell ProliferationAnimalsBone Marrow TransplantationCell MovementCell SurvivalGraft vs Host DiseaseImmunophenotypingInterleukin-2Killer Cells, NaturalL-SelectinLuciferasesLymphoid TissueMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutInterleukin-2L-SelectinLuciferases

Identifiers

PMID19657090
PMCPMC2880476
OpenAlexW1798184081

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.