Evidence map›Paper›PMID 33329524›Full record

ArticleFrontiers in immunology2020

CD4 and CD8 T Cell Memory Interactions Alter Innate Immunity and Organ Injury in the CLP Sepsis Model.

Matthew D Taylor, Tiago D Fernandes, Alexander P Kelly, Mabel N Abraham, Clifford S Deutschman

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. 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
1.6field-weighted citation impact, top 15% 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, 30 citations in OpenAlex.

  1. Article
  2. IL17FMolecular medicine (Cambridge, Mass.) · 2026
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  6. Observational
  7. Article
  8. The clinical trajectory of peripheral blood immune cell subsets, T-cell activation, and cytokines in septic patients.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  9. Article
  10. Article
  11. Evaluation of CD4Emergency medicine international · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Angiotensin II enhances bacterial clearance via myeloid signaling in a murine sepsis model.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
  18. Article
  19. Tim-3 regulates sepsis-induced immunosuppression by inhibiting the NF-κB signaling pathway in CD4 T cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    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

5 authors at 2 institutions in 1 country.

Matthew D TaylorThe Division of Critical Care Medicine, Department of Pediatrics, The Feinstein Institutes for Medical Research, Manhasset, NY, and Cohen Children's Medical Center/Northwell Health, New Hyde Park, NY, United States.
Tiago D FernandesThe Division of Critical Care Medicine, Department of Pediatrics, The Feinstein Institutes for Medical Research, Manhasset, NY, and Cohen Children's Medical Center/Northwell Health, New Hyde Park, NY, United States.
Alexander P KellyThe Division of Critical Care Medicine, Department of Pediatrics, The Feinstein Institutes for Medical Research, Manhasset, NY, and Cohen Children's Medical Center/Northwell Health, New Hyde Park, NY, United States.
Mabel N AbrahamThe Division of Critical Care Medicine, Department of Pediatrics, The Feinstein Institutes for Medical Research, Manhasset, NY, and Cohen Children's Medical Center/Northwell Health, New Hyde Park, NY, United States.
Clifford S DeutschmanThe Division of Critical Care Medicine, Department of Pediatrics, The Feinstein Institutes for Medical Research, Manhasset, NY, and Cohen Children's Medical Center/Northwell Health, New Hyde Park, NY, United States.
Northwell Health · USFeinstein Institute for Medical Research · US

Funding

Orexinergic Modulation of Experimental SepsisR01GM121102 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DEUTSCHMAN, CLIFFORD SCOTT, PAVLOV, VALENTIN ATANASSOV · 2017 to 2020
$1.6M
Effects of Memory T Cells on the Response to Cecal Ligation and PunctureK08GM132794 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI TAYLOR, MATTHEW DAVID · 2019 to 2022
$782k
NIGMS NIH HHS K08 GM132794NIGMS NIH HHS R01 GM121102
6 · The paper itself

Abstract

The role of T cell memory in sepsis is poorly understood. Recent work has demonstrated that mice exposed to frequent antigenic stimulation, in contrast to laboratory mice, better recapitulate the human T cell repertoire. This difference may profoundly alter responses to inflammatory insults. We induced isolated T cell memory by inoculating C57Bl/6 mice with an anti-CD3ϵ activating antibody, a process we term "immune education." These mice were subjected to the cecal ligation and puncture (CLP) model of sepsis and responses were compared to those of isotype-treated controls. CLP-induced increases in 1) CD4 T cell production and serum levels of IFNγ, 2) CD8 T cell granzyme B levels, and 3) innate cell function were all more pronounced in educated mice than in control mice. Immune education increased CLP-induced liver injury and decreased survival. The differences in responses to CLP were not recapitulated in mice with either isolated CD4 or isolated CD8 T cell memory. Relative to controls, CLP in educated CD8

Indexed as

Immunity, InnateImmunologic MemoryAnimalsCD4 AntigensCD4 Lymphocyte CountCD4-Positive T-LymphocytesCD8 AntigensCD8-Positive T-LymphocytesCecumCell CommunicationDisease Models, AnimalInterferon-gammaMaleMiceMice, Inbred C57BLMice, KnockoutCD4 AntigensCD8 AntigensIFNG protein, mouseInterferon-gammaadaptive immunityCD4 T CellsCD8 T cellscecal ligation and punctureinnate immunityorgan dysfunctionsepsisT cell memory

Identifiers

PMID33329524
PMCPMC7715000
OpenAlexW3107810669

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.