Evidence map›Paper›PMID 26195801›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

IL-15 receptor α signaling constrains the development of IL-17-producing γδ T cells.

Sara L Colpitts, Lynn Puddington, Leo Lefrançois

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Transcriptomic Profiling of Plaque Psoriasis and Cutaneous T-Cell Subsets during Treatment with Secukinumab.JID innovations : skin science from molecules to population health · 2022
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Skin Resident γδ T Cell Function and Regulation in Wound Repair.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Immune network · 2018
    Review
  15. Review
  16. Article
  17. Article
  18. IL-17Nature immunology · 2017
    Review
  19. 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

3 authors at 1 institution in 1 country.

Sara L ColpittsDepartment of Immunology, Center for Integrated Immunology and Vaccine Research, UConn Health, Farmington, CT 06030 puddington@uchc.edu Sara.L.Colpitts@Dartmouth.edu.
Lynn PuddingtonDepartment of Immunology, Center for Integrated Immunology and Vaccine Research, UConn Health, Farmington, CT 06030 puddington@uchc.edu Sara.L.Colpitts@Dartmouth.edu.
Leo LefrançoisDepartment of Immunology, Center for Integrated Immunology and Vaccine Research, UConn Health, Farmington, CT 06030.
UConn Health · US

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
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 AI051583NIAID NIH HHS AI056172NIAID NIH HHS P01 AI056172NIAID NIH HHS R01 AI051583NIAID NIH HHS R56 AI051583
6 · The paper itself

Abstract

The development and homeostasis of γδ T cells is highly dependent on distinct cytokine networks. Here we examine the role of IL-15 and its unique receptor, IL-15Rα, in the development of IL-17-producing γδ (γδ-17) T cells. Phenotypic analysis has shown that CD44(high) γδ-17 cells express IL-15Rα and the common gamma chain (CD132), yet lack the IL-2/15Rβ chain (CD122). Surprisingly, we found an enlarged population of γδ-17 cells in the peripheral and mesenteric lymph nodes of adult IL-15Rα KO mice, but not of IL-15 KO mice. The generation of mixed chimeras from neonatal thymocytes indicated that cell-intrinsic IL-15Rα expression was required to limit IL-17 production by γδ T cells. γδ-17 cells also were increased in the peripheral lymph nodes of transgenic knock-in mice, where the IL-15Rα intracellular signaling domain was replaced with the intracellular portion of the IL-2Rα chain (that lacks signaling capacity). Finally, an analysis of neonatal thymi revealed that the CD44(lo/int) precursors of γδ-17 cells, which also expressed IL-15Rα, were increased in newborn mice deficient in IL-15Rα signaling, but not in IL-15 itself. Thus, these findings demonstrate that signaling through IL-15Rα regulates the development of γδ-17 cells early in ontogeny, with long-term effects on their peripheral homeostasis in the adult.

Indexed as

Signal TransductionAnimalsAnimals, NewbornAntigens, CDCell MovementFluorescenceInterleukin-15 Receptor alpha SubunitInterleukin-17Interleukin-2 Receptor alpha SubunitMice, Inbred C57BLMice, KnockoutReceptors, Antigen, T-Cell, gamma-deltaThymus GlandT-LymphocytesAntigens, CDInterleukin-15 Receptor alpha SubunitInterleukin-17Interleukin-2 Receptor alpha SubunitReceptors, Antigen, T-Cell, gamma-deltaIL-15RαIL-17γδ T cells

Identifiers

PMID26195801
PMCPMC4534247
OpenAlexW2124159763

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.