Evidence map›Paper›PMID 31620129›Full record

ArticleFrontiers in immunology2019

Defective Transcriptional Programming of Effector CD8 T Cells in Aged Mice Is Cell-Extrinsic and Can Be Corrected by Administration of IL-12 and IL-18.

Mladen Jergović, Heather L Thompson, Kristin R Renkema, Megan J Smithey, Janko Nikolich-Žugich

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

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  14. Immune response to COVID-19 in older adults.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Mladen JergovićDepartment of Immunobiology and the University of Arizona Center on Aging, University of Arizona College of Medicine-Tucson, Tucson, AZ, United States.
Heather L ThompsonDepartment of Immunobiology and the University of Arizona Center on Aging, University of Arizona College of Medicine-Tucson, Tucson, AZ, United States.
Kristin R RenkemaDepartment of Immunobiology and the University of Arizona Center on Aging, University of Arizona College of Medicine-Tucson, Tucson, AZ, United States.
Megan J SmitheyDepartment of Immunobiology and the University of Arizona Center on Aging, University of Arizona College of Medicine-Tucson, Tucson, AZ, United States.
Janko Nikolich-ŽugichDepartment of Immunobiology and the University of Arizona Center on Aging, University of Arizona College of Medicine-Tucson, Tucson, AZ, United States.
University of Arizona · USGrand Valley State University · US

Funding

The Burden of Chikungunya and Dengue Infection in KenyaU54AI081680 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI MOSES, ASHLEE V. · 2009 to 2013
$40.4M
Thymic and Peripheral Aspects of T Cell Aging and RejuvenationP01AG052359 · NIA · UNIVERSITY OF ARIZONA · PI Jennifer L. Uhrlaub · 2017 to 2026
$23.5M
T Cell Homeostasis and Function in Immune SenescenceR37AG020719 · NIA · UNIVERSITY OF ARIZONA · PI JANKO Z. NIKOLICH · 2018 to 2026
$4.2M
T Cell Homeostasis and Function in Immune SenescenceR01AG020719 · NIA · UNIVERSITY OF ARIZONA · PI NIKOLICH, JANKO Z. · 2001 to 2012
$3.1M
Research Supplement to Impact on CMV Upon T-Cell Aging and Immune DefenseR01AG048021 · NIA · UNIVERSITY OF ARIZONA · PI NIKOLICH, JANKO Z. · 2014 to 2018
$2.6M
NIAID NIH HHS HHSN272201100017CNIAID NIH HHS U54 AI081680NIA NIH HHS P01 AG052359NIA NIH HHS R01 AG020719NIA NIH HHS R01 AG048021NIA NIH HHS R37 AG020719
6 · The paper itself

Abstract

In response to infection with intracellular microorganisms, old mice mobilize decreased numbers of antigen-specific CD8 T cells with reduced expression of effector molecules and impaired cytolytic activity. Molecular mechanisms behind these defects and the cell-intrinsic (affecting naïve CD8 T cells themselves) vs. extrinsic, microenvironmental origin of such defects remain unclear. Using reciprocal transfer experiments of highly purified naïve T cells from adult and old transgenic OT-1 mice, we decisively show that the dominant effect is cell-extrinsic. Naïve adult OT-1 T cells failed to expand and terminally differentiate in the old organism infected with

Indexed as

AgingAnimalsCell DifferentiationInterleukin-12Interleukin-18ListeriosisLymphocyte ActivationMiceMice, TransgenicT-Lymphocytes, CytotoxicTranscription, GeneticInterleukin-12Interleukin-18agingbacterial infectioncytokinescytotoxic T cellsinflammation

Identifiers

PMID31620129
PMCPMC6759569
OpenAlexW2972305266

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.