Evidence map›Paper›PMID 17056533›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2006

Combined IL-15/IL-15Ralpha immunotherapy maximizes IL-15 activity in vivo.

Thomas A Stoklasek, Kimberly S Schluns, Leo Lefrançois

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 227 papers.

0numbers the graph read from it
0cells of the map it votes in
227citing papers in PubMed
–field-weighted citation impact
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

227 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Frontiers in immunology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. The clinical landscape of CAR NK cells.Experimental hematology & oncology · 2025
    Review
  13. Article
  14. IL-15: from discovery to FDA approval.Journal of hematology & oncology · 2025
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

167 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

3 authors.

Thomas A StoklasekDepartment of Immunology, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030, USA.
Kimberly S Schluns
Leo Lefrançois

Funding

Sustained adaptive immunity in the mucosaP01AI056172 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T · 2003 to 2017
$22.3M
Role of IL-15 in CD8 T Cell Development and ResponseR01AI051583 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEFRANCOIS, LEO · 2002 to 2011
$3.1M
BASIC IMMUNOLOGY &IMMUNOLOGIC CELL INJURYT32AI007080 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ADLER, ADAM J, VELLA, ANTHONY T · 1985 to 2012
$1.4M
Role of IL-15 in CD8 T Cell Development and ResponseR56AI051583 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEFRANCOIS, LEO · 2007 to 2007
$370k
NIAID NIH HHS AI 51583NIAID NIH HHS P01 AI056172NIAID NIH HHS P01 AI 56172NIAID NIH HHS R01 AI051583NIAID NIH HHS R56 AI051583NIAID NIH HHS T32 AI007080NIAID NIH HHS T32 AI 07080
6 · The paper itself

Abstract

IL-15 has substantial potential as an immunotherapeutic agent for augmenting immune responses. However, the activity of IL-15 is mediated by a unique mechanism in which the cytokine is transpresented by cell-bound high-affinity IL-15Ralpha to target cells expressing the IL-15Rbeta and the common gamma-chain. Thus, the efficacy of administered IL-15 alone may be limited by the availability of free IL-15Ralpha. We now show that administration of soluble IL-15/IL-15Ralpha complexes greatly enhanced IL-15 half-life and bioavailability in vivo. Treatment of mice with this complex, but not with IL-15 alone, resulted in robust proliferation of memory CD8 T cells, NK cells, and NK T cells. The activity of the complex required IL-15Rbeta, but not IL-15Ralpha, expression by the responding cells and was IL-7-independent. Interestingly, IL-15/IL-15Ralpha immunotherapy also caused naive CD8 T cell activation and development into effector cells and long-term memory T cells. Lastly, complexed IL-15, as compared with IL-15 alone, dramatically reduced tumor burden in a model of B16 melanoma. These findings hold significant importance for the use of IL-15 as a potential adjuvant/therapeutic and inducer of homeostatic proliferation, without the necessity for prior immunodepletion.

Indexed as

Immunologic MemoryImmunotherapyAnimalsCD8-Positive T-LymphocytesCell ProliferationDrug Therapy, CombinationHalf-LifeInterleukin-15Interleukin-2 Receptor beta SubunitInterleukin-7Killer Cells, NaturalLymphocyte ActivationMelanoma, ExperimentalMiceMice, Inbred C57BLReceptors, Interleukin-15Il15ra protein, mouseInterleukin-15Interleukin-2 Receptor beta SubunitInterleukin-7Receptors, Interleukin-15

Identifiers

PMID17056533
PMCPMC2847275

What OpenQuestion holds

Textmetadata
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.