Evidence map›Paper›PMID 19299733›Full record

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

Immunologic and therapeutic synergy of IL-27 and IL-2: enhancement of T cell sensitization, tumor-specific CTL reactivity and complete regression of disseminated neuroblastoma metastases in the liver and bone marrow.

Rosalba Salcedo, Julie A Hixon, Jimmy K Stauffer, Rashmi Jalah, Alan D Brooks, Tahira Khan, Ren-Ming Dai, Loretta Scheetz, Erin Lincoln, Timothy C Back and 8 more

Open access · greenAbstract 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 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

48 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
  2. Senescence-induced p21Cell discovery · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. IL-27 improves adoptive CD8Cancer science · 2022
    Article
  10. A Bayesian network meta-analysis of comparison of cancer therapeutic vaccines for melanoma.Journal of the European Academy of Dermatology and Venereology : JEADV · 2021
    Review
  11. Is AAV-delivered IL-27 a potential immunotherapeutic for cancer?American journal of cancer research · 2020
    Review
  12. IL-27 promotes the expansion of self-renewing CD8The Journal of experimental medicine · 2019
    Article
  13. IL-27 confers a protumorigenic activity of regulatory T cells via CD39.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Combination immunotherapy: a road map.Journal for immunotherapy of cancer · 2017
    Review
  20. Follicular CD8Frontiers in immunology · 2017
    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

18 authors at 6 institutions in 3 countries.

Rosalba SalcedoScience Applications International Corporation, National Cancer Institute-Frederick, MD 21702, USA. lmirosi@ncifcrf.gov
Julie A Hixon
Jimmy K Stauffer
Rashmi Jalah
Alan D Brooks
Tahira Khan
Ren-Ming Dai
Loretta Scheetz
Erin Lincoln
Timothy C Back
Douglas Powell
Arthur A Hurwitz
Thomas J Sayers
Robert Kastelein
George N Pavlakis
Barbara K Felber
Giorgio Trinchieri
Jon M Wigginton
Science Applications International Corporation (United States) · USNational Cancer Institute · USLaboratory of Molecular Genetics · PLOrganogenesis (United States) · USCTI BioPharma (Italy) · ITData Management Services (United States) · US

Funding

Prevention of AIDSZIABC010350 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FELBER, BARBARA K · 2009 to 2025
$30.0M
Immunotherapeutic Approaches for AIDSZIABC010749 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PAVLAKIS, GEORGE N. · 2009 to 2022
$21.6M
Role of inflammation, innate resistance, and immunity in carcinogenesis.ZIABC010793 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TRINCHIERI, GIORGIO · 2009 to 2025
$16.8M
Heterodimeric IL-15 in Cancer ImmunotherapyZIABC010750 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PAVLAKIS, GEORGE N. · 2009 to 2022
$15.6M
Posttranscriptional control of gene expressionZIABC010334 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FELBER, BARBARA K · 2009 to 2025
$15.1M
Tumor Growth and Microenvironment Influence T Cell Tolerance to Tumor AntigensZIABC010954 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HURWITZ, ARTHUR · 2009 to 2015
$3.4M
Mechanisms of Immune-mediated Tumor Cell DestructionZIABC010012 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SAYERS, THOMAS · 2009 to 2018
$3.3M
Intramural NIH HHSNCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400
6 · The paper itself

Abstract

IL-27 exerts antitumor activity in murine orthotopic neuroblastoma, but only partial antitumor effect in disseminated disease. This study demonstrates that combined treatment with IL-2 and IL-27 induces potent antitumor activity in disseminated neuroblastoma metastasis. Complete durable tumor regression was achieved in 90% of mice bearing metastatic TBJ-IL-27 tumors treated with IL-2 compared with only 40% of mice bearing TBJ-IL-27 tumors alone and 0% of mice bearing TBJ-FLAG tumors with or without IL-2 treatment. Comparable antitumor effects were achieved by IL-27 protein produced upon hydrodynamic IL-27 plasmid DNA delivery when combined with IL-2. Although delivery of IL-27 alone, or in combination with IL-2, mediated pronounced regression of neuroblastoma metastases in the liver, combined delivery of IL-27 and IL-2 was far more effective than IL-27 alone against bone marrow metastases. Combined exposure to IL-27 produced by tumor and IL-2 synergistically enhances the generation of tumor-specific CTL reactivity. Potentiation of CTL reactivity by IL-27 occurs via mechanisms that appear to be engaged during both the initial sensitization and effector phase. Potent immunologic memory responses are generated in mice cured of their disseminated disease by combined delivery of IL-27 and IL-2, and depletion of CD8(+) ablates the antitumor efficacy of this combination. Moreover, IL-27 delivery can inhibit the expansion of CD4(+)CD25(+)Foxp3(+) regulatory and IL-17-expressing CD4(+) cells that are otherwise observed among tumor-infiltrating lymphocytes from mice treated with IL-2. These studies demonstrate that IL-27 and IL-2 synergistically induce complete tumor regression and long-term survival in mice bearing widely metastatic neuroblastoma tumors.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsBone Marrow NeoplasmsDrug SynergismFlow CytometryInterferon-gammaInterleukin-2InterleukinsLiver NeoplasmsLymphocyte ActivationLymphocytes, Tumor-InfiltratingMaleMiceNeuroblastomaT-Lymphocytes, CytotoxicIl27 protein, mouseInterferon-gammaInterleukin-2Interleukins

Identifiers

PMID19299733
PMCPMC2730673
OpenAlexW1899758583

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.