Evidence map›Paper›PMID 25780034›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

IL-18 acts in synergy with IL-7 to promote ex vivo expansion of T lymphoid progenitor cells.

Siva K Gandhapudi, Chibing Tan, Julie H Marino, Ashlee A Taylor, Christopher C Pack, Joel Gaikwad, C Justin Van De Wiele, Jonathan D Wren, T Kent Teague

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

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  10. Complex and Multilayered Role of IL-21 Signaling during Thymic Development.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  11. Article
  12. Tetraspanin-enriched microdomains regulate digitation junctions.Cellular and molecular life sciences : CMLS · 2018
    Article
  13. Article
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  15. 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

9 authors at 4 institutions in 1 country.

Siva K GandhapudiDepartment of Surgery, University of Oklahoma School of Community Medicine, Tulsa, OK 74104;
Chibing TanDepartment of Surgery, University of Oklahoma School of Community Medicine, Tulsa, OK 74104;
Julie H MarinoDepartment of Surgery, University of Oklahoma School of Community Medicine, Tulsa, OK 74104;
Ashlee A TaylorDepartment of Surgery, University of Oklahoma School of Community Medicine, Tulsa, OK 74104;
Christopher C PackDepartment of Surgery, University of Oklahoma School of Community Medicine, Tulsa, OK 74104;
Joel GaikwadDepartment of Biological Sciences, Oral Roberts University, Tulsa, OK 74171;
C Justin Van De WieleDepartment of Surgery, University of Oklahoma School of Community Medicine, Tulsa, OK 74104; Department of Pharmaceutical Sciences, University of Oklahoma College of Pharmacy, Tulsa, OK 74135;
Jonathan D WrenDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104; Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104; kent-teague@ouhsc.edu jdwren@gmail.com.
T Kent TeagueDepartment of Surgery, University of Oklahoma School of Community Medicine, Tulsa, OK 74104; Department of Pharmaceutical Sciences, University of Oklahoma College of Pharmacy, Tulsa, OK 74135; Department of Psychiatry, University of Oklahoma School of Community Medicine, Tulsa, OK 74104; and Department of Biochemistry and Microbiology, Oklahoma State University Center for the Health Sciences, Tulsa, OK 74107 kent-teague@ouhsc.edu jdwren@gmail.com.ORCID http://orcid.org/0000-0002-4680-5440
University of Oklahoma · USOklahoma Medical Research Foundation · USOklahoma State University Center for Health Sciences · USOral Roberts University · US

Funding

Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
VALIDATING NOVEL GENES IMPLICATED IN LEUKOCYTE CHEMOTAXISP20RR020143 · NCRR · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI ALARCON-RIQUELME, MARTA E · 2004 to 2011
$21.0M
Quantitative Analysis Core P30GM110766 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI CAPRA, J DONALD · 2014 to 2018
$6.1M
Molecular Mechanisms and Genetics of AutoimmunityP20GM103456 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI GAFFNEY, PATRICK M · 2012 to 2013
$4.8M
NCRR NIH HHS P20 RR020143NIGMS NIH HHS 5P20GM103636NIGMS NIH HHS 8P20GM103456NIGMS NIH HHS P20 GM103456NIGMS NIH HHS P20 GM103636NIGMS NIH HHS P30 GM110766
6 · The paper itself

Abstract

Although IL-18 has not previously been shown to promote T lymphopoiesis, results obtained via a novel data mining algorithm (global microarray meta-analysis) led us to explore a predicted role for this cytokine in T cell development. IL-18 is a member of the IL-1 cytokine family that has been extensively characterized as a mediator of inflammatory immune responses. To assess a potential role for IL-18 in T cell development, we sort-purified mouse bone marrow-derived common lymphoid progenitor cells, early thymic progenitors (ETPs), and double-negative 2 thymocytes and cultured these populations on OP9-Delta-like 4 stromal layers in the presence or absence of IL-18 and/or IL-7. After 1 wk of culture, IL-18 promoted proliferation and accelerated differentiation of ETPs to the double-negative 3 stage, similar in efficiency to IL-7. IL-18 showed synergy with IL-7 and enhanced proliferation of both the thymus-derived progenitor cells and the bone marrow-derived common lymphoid progenitor cells. The synergistic effect on the ETP population was further characterized and found to correlate with increased surface expression of c-Kit and IL-7 receptors on the IL-18-treated cells. In summary, we successfully validated the global microarray meta-analysis prediction that IL-18 affects T lymphopoiesis and demonstrated that IL-18 can positively impact bone marrow lymphopoiesis and T cell development, presumably via interaction with the c-Kit and IL-7 signaling axis.

Indexed as

Interleukin-7LymphopoiesisAnimalsCell DifferentiationCell ProliferationCells, CulturedGene Expression ProfilingGene Expression RegulationInterleukin-18MiceMice, Mutant StrainsOligonucleotide Array Sequence AnalysisPrecursor Cells, T-LymphoidProto-Oncogene Proteins c-kitSignal TransductionInterleukin-18Interleukin-7interleukin-7, mouseProto-Oncogene Proteins c-kit

Identifiers

PMID25780034
PMCPMC4536257
OpenAlexW2104650869

What OpenQuestion holds

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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.