Evidence map›Paper›PMID 15867097›Full record

Trial reportThe Journal of experimental medicine2005

Sustained expansion of NKT cells and antigen-specific T cells after injection of alpha-galactosyl-ceramide loaded mature dendritic cells in cancer patients.

David H Chang, Keren Osman, John Connolly, Anjli Kukreja, Joseph Krasovsky, Maggi Pack, Aisha Hutchinson, Matthew Geller, Nancy Liu, Rebecca Annable and 8 more

Erratum issuedOpen access · bronzeAbstract readClinical TrialComparative Study
In one paragraph

Trial report in The Journal of experimental medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 208 papers.

0numbers the graph read from it
0cells of the map it votes in
208citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

208 citing papers in PubMed, 410 citations in OpenAlex.

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  12. Facts and Hopes of Chimeric Antigen Receptor-Redirected NK T Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Review
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148 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 2 countries.

David H ChangLaboratory of Tumor Immunology and Immunotherapy, The Rockefeller University, New York, NY 10021, USA.
Keren Osman
John Connolly
Anjli Kukreja
Joseph Krasovsky
Maggi Pack
Aisha Hutchinson
Matthew Geller
Nancy Liu
Rebecca Annable
Jennifer Shay
Kelly Kirchhoff
Nobusuke Nishi
Yoshitaka Ando
Kunihiko Hayashi
Hani Hassoun
Ralph M Steinman
Madhav V Dhodapkar
Rockefeller University · USKirin (Japan) · JPMemorial Sloan Kettering Cancer Center · US

Funding

Targeting Dendritic Cells for Enhanced Musocal ImmunityU19AI057234 · NIAID · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 2003 to 2013
$49.2M
WOUND HEALING IN INDIVIDUALS OF DIFFERENT AGE AND GENETIC BACKGROUNDM01RR000102 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 1985 to 2006
$32.8M
Technological Development ComponentU19AI062623 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI MORAN, THOMAS M · 2004 to 2009
$21.3M
Induction of melanoma immunity by dendritic cell subsetsP01CA084512 · NCI · ROCKEFELLER UNIVERSITY · PI BANCHEREAU, JACQUES F · 2000 to 2010
$12.1M
Anti-Tumor immunity in myelomaR01CA106802 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2004 to 2016
$3.3M
NCI NIH HHS CA106802NCI NIH HHS CA84512NCI NIH HHS P01 CA084512NCI NIH HHS R01 CA106802NCRR NIH HHS M01 RR000102NCRR NIH HHS M01-RR00102NIAID NIH HHS 5U19AI057234NIAID NIH HHS U-19 5U19 AI062623
6 · The paper itself

Abstract

Natural killer T (NKT) cells are distinct glycolipid reactive innate lymphocytes that are implicated in the resistance to pathogens and tumors. Earlier attempts to mobilize NKT cells, specifically, in vivo in humans met with limited success. Here, we evaluated intravenous injection of monocyte-derived mature DCs that were loaded with a synthetic NKT cell ligand, alpha-galactosyl-ceramide (alpha-GalCer; KRN-7000) in five patients who had advanced cancer. Injection of alpha-GalCer-pulsed, but not unpulsed, dendritic cells (DCs) led to >100-fold expansion of several subsets of NKT cells in all patients; these could be detected for up to 6 mo after vaccination. NKT activation was associated with an increase in serum levels of interleukin-12 p40 and IFN-gamma inducible protein-10. In addition, there was an increase in memory CD8+ T cells specific for cytomegalovirus in vivo in response to alpha-GalCer-loaded DCs, but not unpulsed DCs. These data demonstrate the feasibility of sustained expansion of NKT cells in vivo in humans, including patients who have advanced cancer, and suggest that NKT activation might help to boost adaptive T cell immunity in vivo.

Indexed as

Cell ProliferationImmunotherapyVaccinationAdultBlood Chemical AnalysisCD8-Positive T-LymphocytesChemokine CXCL10ChemokinesChemokines, CXCCytokinesCytomegalovirusDendritic CellsFlow CytometryGalactosylceramidesHumansInterleukin-12alpha-galactosylceramideChemokine CXCL10ChemokinesChemokines, CXCCytokinesGalactosylceramidesInterleukin-12

Identifiers

PMID15867097
PMCPMC1389847
OpenAlexW2119695630

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.