Evidence map›Paper›PMID 19608394›Full record

ReviewCurrent opinion in immunology2009

Rejuvenation of the aging T cell compartment.

Amanda M Holland, Marcel R M van den Brink

Abstract readReview
In one paragraph

Review in Current opinion in immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.5field-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

37 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Transcription-Related Dynamics from Immune Disability into Endogenous Innovation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Article
  8. Review
  9. Does patient age influence anti-cancer immunity?Seminars in immunopathology · 2019
    Review
  10. mTORC2 in Thymic Epithelial Cells Controls Thymopoiesis and T Cell Development.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
  11. Article
  12. Prolongevity hormone FGF21 protects against immune senescence by delaying age-related thymic involution.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Causes, consequences, and reversal of immune system aging.The Journal of clinical investigation · 2013
    Review
  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

2 authors at 2 institutions in 1 country.

Amanda M HollandDepartment of Immunology and Microbial Pathogenesis, Weill Cornell Medical College, New York, NY 10021, USA.
Marcel R M van den Brink
Cornell University · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
TREATMENT OF CANCER PATIENTS WITH THYMIC FACTORSP01CA033049 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI DIVGI, CHAITANYA R. · 1985 to 2009
$19.8M
Strategies to enhance immune reconstitution after bone marrow transplantR01HL069929 · NHLBI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI VAN DEN BRINK, MARCEL R M · 2002 to 2015
$7.0M
IMMUNOLOGY RESEARCH TRAINING PROGRAMT32AI007621 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI CESARMAN, ETHEL · 1999 to 2014
$3.4M
Strategies to Enhance Lymphoid Recovery After Radiation-Induced InjuryR01AI080455 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI VAN DEN BRINK, MARCEL R M · 2008 to 2012
$2.6M
T cell homing in intestinal graft-versus-host diseaseR01CA107096 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI VAN DEN BRINK, MARCEL R M · 2005 to 2009
$1.6M
NCI NIH HHS P01 CA033049NCI NIH HHS P01-CA33049NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA107096NCI NIH HHS R01-CA107096NHLBI NIH HHS R01 HL069929NHLBI NIH HHS R01-HL069929NIAID NIH HHS R01 AI080455NIAID NIH HHS R01-AI080455NIAID NIH HHS T32 AI007621NIAID NIH HHS T32 AI07621
6 · The paper itself

Abstract

The elderly face significant risk for susceptibility to infection and cancer because of declining immune function. Various agents used in the setting of bone marrow transplantation and aging studies represent promising approaches to combating T cell defects in the aging population. Preclinical and clinical studies on the T cell reconstitution effects of sex steroid ablation, keratinocyte growth factor, the growth hormone pathway, and the cytokines interleukin-7, interleukin-12, and interleukin-15 indicate that these strategies may be used to alleviate the effects of T cell deficiencies in the elderly.

Indexed as

AgingAnimalsBone Marrow TransplantationCytokinesFibroblast Growth Factor 7Gonadal Steroid HormonesGrowth HormoneGuided Tissue RegenerationHumansImmune ToleranceInsulin-Like Growth Factor IMiceRejuvenationT-LymphocytesCytokinesFGF7 protein, humanFibroblast Growth Factor 7Gonadal Steroid HormonesGrowth HormoneInsulin-Like Growth Factor I

Identifiers

PMID19608394
PMCPMC2731988
OpenAlexW2062858069

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.