Evidence map›Paper›PMID 34199501›Full record

ReviewCells2021

Toll-Like Receptor Signaling in the Establishment and Function of the Immune System.

Jahnavi Aluri, Megan A Cooper, Laura G Schuettpelz

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Review
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  11. Review
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  15. Peptide GTSFTTTAER FromFood science & nutrition · 2025
    Article
  16. Identifying genetic errors of immunity due to mosaicism.The Journal of experimental medicine · 2025
    Review
  17. Article
  18. Innate and adaptive immunity in neurodegenerative disease.Cellular and molecular life sciences : CMLS · 2025
    Review
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Jahnavi AluriDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Megan A CooperDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Laura G SchuettpelzDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Washington University in St. Louis · US

Funding

ROLE OF TLR2 IN REGULATING NORMAL AND PREMALIGNANT HEMATOPOIETIC STEM CELLSR01HL134896 · NHLBI · WASHINGTON UNIVERSITY · PI LAURA G. SCHUETTPELZ · 2017 to 2026
$3.5M
NHLBI NIH HHS R01 HL134896
6 · The paper itself

Abstract

Toll-like receptors (TLRs) are pattern recognition receptors that play a central role in the development and function of the immune system. TLR signaling promotes the earliest emergence of hematopoietic cells during development, and thereafter influences the fate and function of both primitive and effector immune cell types. Aberrant TLR signaling is associated with hematopoietic and immune system dysfunction, and both loss- and gain-of- function variants in TLR signaling-associated genes have been linked to specific infection susceptibilities and immune defects. Herein, we will review the role of TLR signaling in immune system development and the growing number of heritable defects in TLR signaling that lead to inborn errors of immunity.

Indexed as

Genetic Diseases, InbornImmune System DiseasesSignal TransductionToll-Like ReceptorsAnimalsHumansToll-Like Receptorsimmune systeminborn errors of immunityTLR

Identifiers

PMID34199501
PMCPMC8228919
OpenAlexW3170616931

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.