Evidence map›Paper›PMID 22118527›Full record

ArticleImmunity2011

An interleukin-21-interleukin-10-STAT3 pathway is critical for functional maturation of memory CD8+ T cells.

Weiguo Cui, Ying Liu, Jason S Weinstein, Joseph Craft, Susan M Kaech

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 278 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
278citing papers in PubMed, 3 pooled it
12.4field-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

278 citing papers in PubMed, 3 syntheses or guidelines pooled it, 390 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Article
  10. CD8Cell reports. Medicine · 2026
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Regulators of CD8Nature reviews. Immunology · 2026
    Review
  17. Review
  18. Article
  19. Review
  20. Review

218 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Weiguo CuiDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.
Ying Liu
Jason S Weinstein
Joseph Craft
Susan M Kaech
Yale University · USHoward Hughes Medical Institute · US

Funding

Regulation of memory CD8 T cell developmentR01AI066232 · NIAID · YALE UNIVERSITY · PI Diana Clare Hargreaves · 2005 to 2026
$5.7M
GENETIC ANALYSIS OF T CELLS IN LUPUSR01AR044076 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 1996 to 2010
$4.1M
MOLECULAR CHARACTERIZATION OF THE SNRNP POLYPEPTIDESR01AR040072 · NIAMS · YALE UNIVERSITY · PI Joseph Edgar Craft · 1990 to 2026
$2.5M
Dissecting the role for IL-15 in CD8+ T cell homeostasis in human lupusR01AI075157 · NIAID · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2008 to 2012
$2.0M
Control of Effector and Memory T Cell Development by Inflammatory SignalsR01AI074699 · NIAID · YALE UNIVERSITY · PI KAECH, SUSAN M · 2009 to 2013
$2.0M
Determining how adjuvants alter effector and memory T cells during vaccinationR21AI081150 · NIAID · YALE UNIVERSITY · PI KAECH, SUSAN M · 2009 to 2010
$433k
Howard Hughes Medical InstituteNIAID NIH HHS AI075157NIAID NIH HHS R01 AI066232NIAID NIH HHS R01AI066232NIAID NIH HHS R01 AI074699NIAID NIH HHS R01 AI075157NIAID NIH HHS R21 AI081150NIAID NIH HHS R21AI081150NIAMS NIH HHS AR44076NIAMS NIH HHS R01 AR040072NIAMS NIH HHS R01 AR044076NIAMS NIH HHS R01AR40072
6 · The paper itself

Abstract

Memory CD8(+) T cells are critical for long-term immunity, but the genetic pathways governing their formation remain poorly defined. This study shows that the IL-10-IL-21-STAT3 pathway is critical for memory CD8(+) T cell development after acute LCMV infection. In the absence of either interleukin-10 (IL-10) and IL-21 or STAT3, virus-specific CD8(+) T cells retain terminal effector (TE) differentiation states and fail to mature into protective memory T cells that contain self-renewing central memory T cells. Expression of Eomes, BCL-6, Blimp-1, and SOCS3 was considerably reduced in STAT3-deficient memory CD8(+) T cells, and BCL-6- or SOCS3-deficient CD8(+) T cells also had perturbed memory cell development. Reduced SOCS3 expression rendered STAT3-deficient CD8(+) T cells hyperresponsive to IL-12, suggesting that the STAT3-SOCS3 pathway helps to insulate memory precursor cells from inflammatory cytokines that drive TE differentiation. Thus, memory CD8(+) T cell precursor maturation is an active process dependent on IL-10-IL-21-STAT3 signaling.

Indexed as

Signal TransductionAnimalsCD8-Positive T-LymphocytesCell DifferentiationGene Expression Regulation, DevelopmentalImmunologic MemoryInterleukin-10Interleukin-21InterleukinsMiceMice, KnockoutPositive Regulatory Domain I-Binding Factor 1Proto-Oncogene Proteins c-bcl-6STAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling ProteinsEomes protein, mouseInterleukin-10Interleukin-21InterleukinsPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseProto-Oncogene Proteins c-bcl-6Socs3 protein, mouseSTAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling ProteinsT-Box Domain ProteinsTranscription Factors

Identifiers

PMID22118527
PMCPMC3431922
OpenAlexW1973601490

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.