Evidence map›Paper›PMID 27183627›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Inflammatory Signals Regulate IL-15 in Response to Lymphodepletion.

Scott M Anthony, Sarai C Rivas, Sara L Colpitts, Megan E Howard, Spencer W Stonier, Kimberly S Schluns

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

24 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Article
  3. Intraperitoneal infusion of NKG2D CAR-NK cells induces endogenous CD8Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  4. Review
  5. Results From First-in-Human Phase I Study of a Novel CD19-1XX Chimeric Antigen Receptor With Calibrated Signaling in Large B-Cell Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. NK Cell-Derived IL-10 Supports Host Survival during Sepsis.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  15. Review
  16. Review
  17. Article
  18. Control of memory CD8Molecular immunology · 2020
    Review
  19. Article
  20. IL-15 is a component of the inflammatory milieu in the tumor microenvironment promoting antitumor responses.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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

6 authors at 2 institutions in 1 country.

Scott M AnthonyImmunology Graduate Program, University of Texas Graduate School of Biomedical Sciences at Houston, Houston, TX 77030; Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77030; and.ORCID 0000-0002-1590-7401
Sarai C RivasDepartment of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77030; and.ORCID 0000-0002-6432-5600
Sara L ColpittsDepartment of Immunology, University of Connecticut Health Science Center, Farmington, CT 06030.
Megan E HowardDepartment of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77030; and.
Spencer W StonierImmunology Graduate Program, University of Texas Graduate School of Biomedical Sciences at Houston, Houston, TX 77030; Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77030; and.ORCID 0000-0003-4540-3279
Kimberly S SchlunsImmunology Graduate Program, University of Texas Graduate School of Biomedical Sciences at Houston, Houston, TX 77030; Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77030; and kschluns@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USUConn Health · US

Funding

Training Program in Cancer ImmunobiologyT32CA009598 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ALLISON, JAMES P · 1988 to 2014
$4.9M
NCI NIH HHS T32 CA009598
6 · The paper itself

Abstract

Induction of lymphopenia has been exploited therapeutically to improve immune responses to cancer therapies and vaccinations. Whereas IL-15 has well-established roles in stimulating lymphocyte responses after lymphodepletion, the mechanisms regulating these IL-15 responses are unclear. We report that cell surface IL-15 expression is upregulated during lymphopenia induced by total body irradiation (TBI), cyclophosphamide, or Thy1 Ab-mediated T cell depletion, as well as in RAG(-/-) mice; interestingly, the cellular profile of surface IL-15 expression is distinct in each model. In contrast, soluble IL-15 (sIL-15) complexes are upregulated only after TBI or αThy1 Ab. Analysis of cell-specific IL-15Rα conditional knockout mice revealed that macrophages and dendritic cells are important sources of sIL-15 complexes after TBI but provide minimal contribution in response to Thy1 Ab treatment. Unlike with TBI, induction of sIL-15 complexes by αThy1 Ab is sustained and only partially dependent on type I IFNs. The stimulator of IFN genes pathway was discovered to be a potent inducer of sIL-15 complexes and was required for optimal production of sIL-15 complexes in response to Ab-mediated T cell depletion and TBI, suggesting products of cell death drive production of sIL-15 complexes after lymphodepletion. Lastly, we provide evidence that IL-15 induced by inflammatory signals in response to lymphodepletion drives lymphocyte responses, as memory CD8 T cells proliferated in an IL-15-dependent manner. Overall, these studies demonstrate that the form in which IL-15 is expressed, its kinetics and cellular sources, and the inflammatory signals involved are differentially dictated by the manner in which lymphopenia is induced.

Indexed as

Lymphocyte DepletionAnimalsDisease Models, AnimalInflammationInterleukin-15Lymphocyte ActivationLymphopeniaMiceMice, Inbred C57BLMice, KnockoutInterleukin-15

Identifiers

PMID27183627
PMCPMC4875792
OpenAlexW2339180380

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.