Evidence map›Paper›PMID 26147684›Full record

ArticleNature immunology2015

Production of IL-10 by CD4(+) regulatory T cells during the resolution of infection promotes the maturation of memory CD8(+) T cells.

Brian J Laidlaw, Weiguo Cui, Robert A Amezquita, Simon M Gray, Tianxia Guan, Yisi Lu, Yasushi Kobayashi, Richard A Flavell, Steven H Kleinstein, Joe Craft and 1 more

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed
9.7field-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

130 citing papers in PubMed, 194 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Regulators of CD8Nature reviews. Immunology · 2026
    Review
  5. Review
  6. Article
  7. EomesoderminImmunity · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Acellular Pertussis Vaccines Induce CD8European journal of immunology · 2025
    Article
  13. Article
  14. Anti-CTLA-4 generates greater memory response than anti-PD-1 via TCF-1.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Meeting the Challenge of Controlling Viral Immunopathology.International journal of molecular sciences · 2024
    Review
  20. Article

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

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

11 authors at 2 institutions in 1 country.

Brian J LaidlawDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.
Weiguo CuiDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.
Robert A Amezquita1] Department of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA. [2] Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
Simon M GrayDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.
Tianxia GuanDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.
Yisi LuDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.
Yasushi KobayashiDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.
Richard A Flavell1] Department of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA. [2] Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
Steven H Kleinstein1] Department of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA. [2] Department of Pathology, Yale School of Medicine, New Haven, Connecticut, USA. [3] Interdepartmental Program in Computational Biology and Bioinformatics, Yale School of Medicine, New Haven, Connecticut, USA.
Joe Craft1] Department of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA. [2] Department of Internal Medicine (Rheumatology), Yale School of Medicine, New Haven, Connecticut, USA.
Susan M Kaech1] Department of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA. [2] Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
Yale University · USHoward Hughes Medical Institute · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007205 · NIGMS · YALE UNIVERSITY · PI KAZMIERCZAK, BARBARA I · 1985 to 2019
$42.9M
INTERDISCIPLINARY IMMUNOLOGY TRAINING PROGRAMT32AI007019 · NIAID · YALE UNIVERSITY · PI Carrie L. Lucas, David G. Schatz · 1985 to 2026
$14.4M
IMMUNE RESPONSES IN LUPUSR37AR040072 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2000 to 2025
$7.4M
Yale Rheumatic Diseases Research Core CenterP30AR053495 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2007 to 2017
$7.0M
Regulation of memory CD8 T cell developmentR01AI066232 · NIAID · YALE UNIVERSITY · PI Diana Clare Hargreaves · 2005 to 2026
$5.7M
Regulation of memory CD8 T cell developmentR37AI066232 · NIAID · YALE UNIVERSITY · PI KAECH, SUSAN M · 2013 to 2022
$5.4M
MOLECULAR CHARACTERIZATION OF THE SNRNP POLYPEPTIDESR01AR040072 · NIAMS · YALE UNIVERSITY · PI Joseph Edgar Craft · 1990 to 2026
$2.5M
Control of Effector and Memory T Cell Development by Inflammatory SignalsR01AI074699 · NIAID · YALE UNIVERSITY · PI KAECH, SUSAN M · 2009 to 2013
$2.0M
Follicular Helper T Cells in immunity, Allergy and AutoimmunityR21AR068662 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2015 to 2016
$423k
Manipulation of Follicular Helper T Cells in Immunity and AutoimmunityR21AR063942 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2012 to 2013
$402k
Deciphering the signals regulating flu-specific resident memory T cellsF31AG047777 · NIA · YALE UNIVERSITY · PI LAIDLAW, BRIAN · 2014 to 2014
$43k
Howard Hughes Medical InstituteNIAID NIH HHS R01 AI066232NIAID NIH HHS R01AI066232NIAID NIH HHS R01 AI074699NIAID NIH HHS R01AI074699NIAID NIH HHS R37 AI066232NIAID NIH HHS T32 AI007019NIAID NIH HHS T32AI07019NIAMS NIH HHS P30 AR053495NIAMS NIH HHS P30AR053495NIAMS NIH HHS R01 AR040072NIAMS NIH HHS R01AR40072NIAMS NIH HHS R21 AR063942NIAMS NIH HHS R21AR063942NIAMS NIH HHS R21 AR068662NIAMS NIH HHS R37 AR040072NIA NIH HHS F31 AG047777NIA NIH HHS F31AG07777NIGMS NIH HHS T32 GM007205NIGMS NIH HHS T32GM07205
6 · The paper itself

Abstract

Memory CD8(+) T cells are critical for host defense upon reexposure to intracellular pathogens. We found that interleukin 10 (IL-10) derived from CD4(+) regulatory T cells (Treg cells) was necessary for the maturation of memory CD8(+) T cells following acute infection with lymphocytic choriomeningitis virus (LCMV). Treg cell-derived IL-10 was most important during the resolution phase, calming inflammation and the activation state of dendritic cells. Adoptive transfer of IL-10-sufficient Treg cells during the resolution phase 'restored' the maturation of memory CD8(+) T cells in IL-10-deficient mice. Our data indicate that Treg cell-derived IL-10 is needed to insulate CD8(+) T cells from inflammatory signals, and reveal that the resolution phase of infection is a critical period that influences the quality and function of developing memory CD8(+) T cells.

Indexed as

Adoptive TransferAnimalsCD8-Positive T-LymphocytesDendritic CellsFlow CytometryGene Expression ProfilingHost-Pathogen InteractionsImmunologic MemoryInflammationInterleukin-10Lymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMice, Inbred C57BLMice, KnockoutReverse Transcriptase Polymerase Chain ReactionT-Lymphocytes, RegulatoryIL10 protein, mouseInterleukin-10

Identifiers

PMID26147684
PMCPMC4713030
OpenAlexW1511837220

What OpenQuestion holds

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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.