Evidence map›Paper›PMID 23225163›Full record

ArticleEuropean journal of immunology2013

IL-27 enhances the survival of tumor antigen-specific CD8+ T cells and programs them into IL-10-producing, memory precursor-like effector cells.

Zhenzhen Liu, Jin-Qing Liu, Fatemeh Talebian, Lai-Chu Wu, Shulin Li, Xue-Feng Bai

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. IL-27 effects on HIVFrontiers in virology (Lausanne, Switzerland) · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. IL-27 improves adoptive CD8Cancer science · 2022
    Article
  16. Article
  17. Intratumoral delivery of IL-12 and IL-27 mRNA using lipid nanoparticles for cancer immunotherapy.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  18. Article
  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

6 authors at 3 institutions in 1 country.

Zhenzhen LiuDepartment of Pathology and Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Jin-Qing Liu
Fatemeh Talebian
Lai-Chu Wu
Shulin Li
Xue-Feng Bai
The Ohio State University · USThe Ohio State University Wexner Medical Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

The role of CD200 in T cell therapy of cancerR01CA138427 · NCI · OHIO STATE UNIVERSITY · PI BAI, XUE-FENG · 2009 to 2012
$981k
NCI NIH HHS R01 CA138427NCI NIH HHS R01CA138427
6 · The paper itself

Abstract

IL-27 is a member of the IL-12 family of cytokines that is comprised of an IL-12 p40-related protein subunit, EBV-induced gene 3, and a p35-related subunit, p28. IL-27 functions through IL-27R and has been shown to have potent antitumor activity via activation of a variety of cellular components, including antitumor CD8(+) T-cell responses. However, the exact mechanisms of how IL-27 enhances antitumor CD8(+) T-cell responses remain unclear. Here we show that IL-27 significantly enhances the survival of activated tumor antigen-specific CD8(+) T cells in vitro and in vivo, and programs tumor antigen-specific CD8(+) T cells into memory precursor-like effector cells, characterized by upregulation of Bcl-6, SOCS3, Sca-1, and IL-10. While STAT3 activation and the CTL survival-enhancing effects can be independent of CTL IL-10 production, we show here that IL-27-induced CTL IL-10 production contributes to memory precursor cell phenotype induction, CTL memory, and tumor rejection. Thus, IL-27 enhances antitumor CTL responses via programming tumor antigen-specific CD8(+) T cells into a unique memory precursor type of effector cells characterized by a greater survival advantage. Our results have important implications for designing immunotherapy against human cancer.

Indexed as

AnimalsAntigens, LyAntigens, NeoplasmCD8-Positive T-LymphocytesCell Line, TumorCell SurvivalImmunologic MemoryInterleukin-10InterleukinsMembrane ProteinsMiceMice, Inbred BALB CProto-Oncogene Proteins c-bcl-6STAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling ProteinsAntigens, LyAntigens, NeoplasmIL10 protein, mouseIl27 protein, mouseInterleukin-10InterleukinsLy6a protein, mouseMembrane ProteinsProto-Oncogene Proteins c-bcl-6Socs3 protein, mouseStat3 protein, mouseSTAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling Proteins

Identifiers

PMID23225163
PMCPMC3625660
OpenAlexW1590207521

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.