Evidence map›Paper›PMID 31341076›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Complex and Multilayered Role of IL-21 Signaling during Thymic Development.

Magali M Moretto, SuJin Hwang, Keer Chen, Imtiaz A Khan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

4 authors at 2 institutions in 1 country.

Magali M MorettoDepartment of Microbiology, Immunology, and Tropical Medicine, The George Washington University, Washington, DC 20037; and morettom@gwu.edu.ORCID 0000-0001-7268-0998
SuJin HwangDepartment of Laboratory Medicine, National Institutes of Health Clinical Center, Bethesda, MD 20892.ORCID 0000-0001-8531-4575
Keer ChenDepartment of Microbiology, Immunology, and Tropical Medicine, The George Washington University, Washington, DC 20037; and.ORCID 0000-0002-1593-9921
Imtiaz A KhanDepartment of Microbiology, Immunology, and Tropical Medicine, The George Washington University, Washington, DC 20037; and.ORCID 0000-0002-0663-9556
George Washington University · USNational Institutes of Health Clinical Center · US

Funding

LONG TERM IMMUNITY AGAINST TOXOPLASMOSISR01AI033325 · NIAID · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI KHAN, IMTIAZ AHMED · 1998 to 2020
$6.2M
NIAID NIH HHS R01 AI033325
6 · The paper itself

Abstract

Unlike IL-7, which is known to be critical for T cell thymic development, the role of IL-21 in this process is still controversial. IL-21 has been shown to accelerate thymic recovery in mice treated with glucocorticoids and revives the peripheral T cell pool in aged animals. However, mice with a defect in IL-21 signaling exhibit normal thymic cellularity, challenging the importance of this cytokine in the thymic developmental process. Using mixed bone marrow chimeric mice, our studies describe a multilayered role for IL-21 in thymopoiesis. In this system, IL-21R-deficient cells are unable to compete with wild-type populations at different stages of the thymic development. Using a mixed bone marrow chimeric animal model, IL-21 seems to be involved as early as the double-negative 1 stage, and the cells from the knockout compartment have problems transitioning to subsequent double-negative stages. Also, similar to IL-7, IL-21 seems to be involved in the positive selection of double-positive lymphocytes and appears to play a role in the migration of single-positive T cells to the periphery. Although not as critical as IL-7, based on our studies, IL-21 plays an important complementary role in thymic T cell development, which, to date, has been underrecognized.

Indexed as

AnimalsBone MarrowCell DifferentiationInterleukin-21Interleukin-7InterleukinsLymphocytesMiceMice, Inbred C57BLSignal TransductionThymus GlandT-LymphocytesInterleukin-21Interleukin-7Interleukins

Identifiers

PMID31341076
PMCPMC6702097
OpenAlexW2962923223

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.