Evidence map›Paper›PMID 26597007›Full record

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

IL-21 Is Important for Induction of KLRG1+ Effector CD8 T Cells during Acute Intracellular Infection.

Magali M Moretto, Imtiaz A Khan

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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. C5aRNPJ vaccines · 2023
    Article
  5. Article
  6. CTLs Get SMAD When Pathogens Tell Them Where to Go.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  7. Immune Response to Microsporidia.Experientia supplementum (2012) · 2022
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Complex and Multilayered Role of IL-21 Signaling during Thymic Development.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  14. Interleukin (IL)-21 in Inflammation and Immunity During Parasitic Diseases.Frontiers in cellular and infection microbiology · 2019
    Review
  15. IL-21 Selectively Protects CD62LJournal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Magali M MorettoDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, D.C. 20037.
Imtiaz A KhanDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, D.C. 20037 imti56@gwu.edu.ORCID http://orcid.org/0000-0002-0663-9556
George Washington University · US

Funding

CD8+ T cell effectors against microsporidiaR01AI096978 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI KHAN, IMTIAZ AHMED · 2012 to 2015
$1.6M
IL-21 dependent immunity to microsporidiaR56AI102711 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI KHAN, IMTIAZ AHMED · 2013 to 2013
$389k
NIAID NIH HHS AI-096978NIAID NIH HHS AI-102711NIAID NIH HHS R01 AI096978NIAID NIH HHS R56 AI102711
6 · The paper itself

Abstract

Microsporidia, a latent opportunistic infection associated with mild inflammation, is characterized by a strong CD8 T cell response, which has been shown to be CD4 T cell dependent. In this manuscript, we demonstrate that CD4 help is provided via IL-21 production, a common γ-chain cytokine closely related to IL-2. The peak of IL-21 expression, observed during the acute infection, is associated with an elevated IL-21(+) CD4 T subset, and these cells bear a phenotypic resemblance to T follicular helper cells. We observed that, during per-oral microsporidial infection, IL-21 was critical for the generation of an optimal effector CD8 T cell immunity. Sharply decreased effector KLRG1(+) CD8 response was observed in IL-21R knockout mice, and although these cells exhibited reduced functional properties, they retained the ability to proliferate. The role of IL-21 in the generation of CD8 effectors was cell intrinsic, as stronger defects were observed in the IL-21-deficient compartment from the bone marrow chimeric mice (IL-21R knockout/wild-type). These findings are different from those reported for viral infections in which IL-21 has been primarily associated with the generation and maintenance of CD8 memory response. To the best of our knowledge, this report demonstrates a critical role for IL-21 in the generation of a primary effector CD8 T cell response to an infectious disease model.

Indexed as

AnimalsCD8-Positive T-LymphocytesEncephalitozoon cuniculiEncephalitozoonosisInterleukin-21InterleukinsLectins, C-TypeMiceMice, Inbred C57BLMice, KnockoutReceptors, ImmunologicReceptors, Interleukin-21Signal TransductionT-Lymphocytes, Helper-InducerInterleukin-21InterleukinsKlrg1 protein, mouseLectins, C-TypeReceptors, ImmunologicReceptors, Interleukin-21

Identifiers

PMID26597007
PMCPMC4959448
OpenAlexW2174393449

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.