Evidence map›Paper›PMID 27131432›Full record

ReviewTrends in immunology2016

Memory CD8(+) T Cells: Innate-Like Sensors and Orchestrators of Protection.

Grégoire Lauvau, Marie Boutet, Tere M Williams, Shu Shien Chin, Laurent Chorro

Abstract readReview
In one paragraph

Review in Trends in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Article
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  4. Article
  5. Review
  6. Article
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  9. Article
  10. Chemokine Signatures of Pathogen-Specific T Cells I: Effector T Cells.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  11. Article
  12. Metabolic programs define dysfunctional immune responses in severe COVID-19 patients.medRxiv : the preprint server for health sciences · 2020
    Article
  13. Review
  14. CD4Nature communications · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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.

Grégoire LauvauAlbert Einstein College of Medicine, Department of Microbiology and Immunology, New York, NY, USA. Electronic address: gregoire.lauvau@einstein.yu.edu.
Marie BoutetAlbert Einstein College of Medicine, Department of Microbiology and Immunology, New York, NY, USA.
Tere M WilliamsAlbert Einstein College of Medicine, Department of Microbiology and Immunology, New York, NY, USA.
Shu Shien ChinAlbert Einstein College of Medicine, Department of Microbiology and Immunology, New York, NY, USA.
Laurent ChorroAlbert Einstein College of Medicine, Department of Microbiology and Immunology, New York, NY, USA.

Funding

Enhancing Pathogen-specific Memory CD8+ T cell Responses in VivoR01AI103338 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI LAUVAU, GREGOIRE STEPHANE · 2013 to 2022
$5.2M
Geographic Medicine and Emerging InfectionsT32AI070117 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WEISS, LOUIS M. · 2008 to 2023
$5.1M
Enhancing RNAi delivery in vivoR01AI099567 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI LAUVAU, GREGOIRE STEPHANE · 2012 to 2016
$2.1M
A novel siRNA therapeutic to prevent scarring and bleb failure after trabeculectomyR44EY038138 · NEI · DUB THERAPEUTICS INC. · PI Tere M. Williams · 2025 to 2026
$2.0M
A single dose anti-scarring therapeutic for the corneaR44EY035188 · NEI · DUB THERAPEUTICS INC. · PI WILLIAMS, TERE M. · 2023 to 2024
$1.8M
NEI NIH HHS R44 EY035188NEI NIH HHS R44 EY038138NIAID NIH HHS R01 AI099567NIAID NIH HHS R01 AI103338NIAID NIH HHS T32 AI070117
6 · The paper itself

Abstract

Recent findings have revealed roles for systemic and mucosa-resident memory CD8(+) T cells in the orchestration of innate immune responses critical to host defense upon microbial infection. Here we integrate these findings into the current understanding of the molecular and cellular signals controlling memory CD8(+) T cell reactivation and the mechanisms by which these cells mediate effective protection in vivo. The picture that emerges presents memory CD8(+) T cells as early sensors of danger signals, mediating protective immunity both through licensing of cellular effectors of the innate immune system and via the canonical functions associated with memory T cells. We discuss implications for the development of T cell vaccines and therapies and highlight important areas in need of further investigation.

Indexed as

Immunity, MucosalImmunologic MemoryAnimalsCD8-Positive T-LymphocytesHumansImmunotherapy, AdoptiveIntestinal MucosaLymphocyte SubsetsReceptors, Pattern RecognitionVaccinesReceptors, Pattern RecognitionVaccines

Identifiers

PMID27131432
PMCPMC4885763

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.