Evidence map›Paper›PMID 12070281›Full record

ArticleThe Journal of experimental medicine2002

Overexpression of interleukin (IL)-7 leads to IL-15-independent generation of memory phenotype CD8+ T cells.

William C Kieper, Joyce T Tan, Brea Bondi-Boyd, Laurent Gapin, Jonathan Sprent, Rhodri Ceredig, Charles D Surh

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

112 citing papers in PubMed, 280 citations in OpenAlex.

  1. Trial
  2. Article
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  6. Review
  7. Review
  8. Modifying enzyme replacement therapy - A perspective.Journal of cellular and molecular medicine · 2023
    Review
  9. Metabolic dynamics instruct CD8European journal of immunology · 2022
    Review
  10. Article
  11. Homeostasis of Naive and Memory T Lymphocytes.Cold Spring Harbor perspectives in biology · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

William C KieperDepartment of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Joyce T Tan
Brea Bondi-Boyd
Laurent Gapin
Jonathan Sprent
Rhodri Ceredig
Charles D Surh
Scripps Research Institute · USInserm · FRLa Jolla Institute for Immunology · US

Funding

PATHOGENESIS AND IMMUNOLOGY OF DISEASET32AI007244 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 1985 to 2022
$8.8M
REGULATION OF T CELL HOMEOSTASIS AND SURVIVALR01AI045809 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI SURH, CHARLES D. · 2000 to 2009
$4.3M
LYMPHOCYTE FUNCTION IN NORMAL AND CHIMERIC MICER37CA038355 · NCI · SCRIPPS RESEARCH INSTITUTE · PI SPRENT, JONATHAN · 1988 to 2005
$3.1M
T CELL TURNOVER AND THE ROLE OF CYTOKINESR01AI046710 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI SPRENT, JONATHAN · 2000 to 2004
$2.4M
THYMUS AND CENTRAL TOLERANCER01AI021487 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI SPRENT, JONATHAN · 1985 to 2003
$1.9M
Homeostasis of Mature T Cells in the AgedR01AG020186 · NIA · SCRIPPS RESEARCH INSTITUTE · PI SURH, CHARLES D · 2002 to 2005
$1.3M
FUNCTION OF T CELLS FROM H2-M DEFICIENT MICER01AI041079 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI SURH, CHARLES D · 1997 to 2000
$222k
LYMPHOCYTE FUNCTION IN NORMAL AND CHIMERIC MICER01CA038355 · NCI · SCRIPPS CLINIC AND RESEARCH FOUNDATION · PI SPRENT, JONATHAN · 1985 to 1987
–
NCI NIH HHS CA38355NCI NIH HHS R37 CA038355NHLBI NIH HHS HL07196NIAID NIH HHS AI07244NIAID NIH HHS AI21487NIAID NIH HHS AI41079NIAID NIH HHS AI45809NIAID NIH HHS AI46710NIAID NIH HHS R01 AI045809NIAID NIH HHS R01 AI046710NIAID NIH HHS T32 AI007244NIA NIH HHS AG20186NIA NIH HHS R01 AG020186
6 · The paper itself

Abstract

Transgenic (TG) mice expressing a high copy number of interleukin (IL)-7 cDNA under the control of the major histocomaptability complex (MHC) class II promoter display a 10-20-fold increase in total T cell numbers. Here, we show that the increase in T cell numbers in IL-7 TG mice is most apparent at the level of memory phenotype CD44hi CD122hi CD8+ cells. Based on studies with T cell receptor (TCR) TG mice crossed to IL-7 TG mice, increased levels of IL-7 may provide costimulation for TCR recognition of self-MHC ligands and thus cause naive CD8+ cells to proliferate and differentiate into memory phenotype cells. In addition, a marked increase in CD44hi CD122hi CD8+ cells was found in IL-7 TG IL-15(-) mice. Since these cell are rare in normal IL-15(-) mice, the dependency of memory phenotype CD8+ cells on IL-15 can be overcome by overexpression of IL-7.

Indexed as

AnimalsCD8-Positive T-LymphocytesFlow CytometryImmunologic MemoryImmunophenotypingInterleukin-15Interleukin-7MiceMice, Inbred C57BLMice, TransgenicInterleukin-15Interleukin-7

Identifiers

PMID12070281
PMCPMC2193553
OpenAlexW2147246759

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.