Evidence map›Paper›PMID 34305934›Full record

ReviewFrontiers in immunology2021

TIRAP in the Mechanism of Inflammation.

Sajjan Rajpoot, Kishore K Wary, Rachel Ibbott, Dongfang Liu, Uzma Saqib, Teresa L M Thurston, Mirza S Baig

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

51 citing papers in PubMed, 63 citations in OpenAlex.

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  18. Role of TLRs as signaling cascades to combat infectious diseases: a review.Cellular and molecular life sciences : CMLS · 2025
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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

7 authors at 4 institutions in 3 countries.

Sajjan RajpootDepartment of Biosciences and Biomedical Engineering (BSBE), Indian Institute of Technology Indore (IITI), Indore, India.
Kishore K WaryDepartment of Pharmacology and Regenerative Medicine, The University of Illinois at Chicago, Chicago, IL, United States.
Rachel IbbottMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United Kingdom.
Dongfang LiuDepartment of Pathology, Immunology and Laboratory Medicine, Rutgers University-New Jersey Medical School, Newark, NJ, United States.
Uzma SaqibDiscipline of Chemistry, Indian Institute of Technology Indore (IITI), Indore, India.
Teresa L M ThurstonMRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United Kingdom.
Mirza S BaigDepartment of Biosciences and Biomedical Engineering (BSBE), Indian Institute of Technology Indore (IITI), Indore, India.
Indian Institute of Technology Indore · INImperial College London · GBRutgers HealthUniversity of Illinois Chicago · US

Funding

Biotechnology and Biological Sciences Research Council BB/R011834/1
6 · The paper itself

Abstract

The Toll-interleukin-1 Receptor (TIR) domain-containing adaptor protein (TIRAP) represents a key intracellular signalling molecule regulating diverse immune responses. Its capacity to function as an adaptor molecule has been widely investigated in relation to Toll-like Receptor (TLR)-mediated innate immune signalling. Since the discovery of TIRAP in 2001, initial studies were mainly focused on its role as an adaptor protein that couples Myeloid differentiation factor 88 (MyD88) with TLRs, to activate MyD88-dependent TLRs signalling. Subsequent studies delineated TIRAP's role as a transducer of signalling events through its interaction with non-TLR signalling mediators. Indeed, the ability of TIRAP to interact with an array of intracellular signalling mediators suggests its central role in various immune responses. Therefore, continued studies that elucidate the molecular basis of various TIRAP-protein interactions and how they affect the signalling magnitude, should provide key information on the inflammatory disease mechanisms. This review summarizes the TIRAP recruitment to activated receptors and discusses the mechanism of interactions in relation to the signalling that precede acute and chronic inflammatory diseases. Furthermore, we highlighted the significance of TIRAP-TIR domain containing binding sites for several intracellular inflammatory signalling molecules. Collectively, we discuss the importance of the TIR domain in TIRAP as a key interface involved in protein interactions which could hence serve as a therapeutic target to dampen the extent of acute and chronic inflammatory conditions.

Indexed as

Agammaglobulinaemia Tyrosine KinaseAnimalsCarrier ProteinsClass Ia Phosphatidylinositol 3-KinaseHumansImmunity, InnateInflammationMembrane GlycoproteinsModels, BiologicalProtein Interaction MapsProtein Kinase C-deltaReceptor for Advanced Glycation End ProductsReceptors, Interleukin-1Signal TransductionAgammaglobulinaemia Tyrosine KinaseAGER protein, humanBTK protein, humanCarrier ProteinsClass Ia Phosphatidylinositol 3-KinaseMembrane GlycoproteinsODF2L protein, humanProtein Kinase C-deltaReceptor for Advanced Glycation End ProductsReceptors, Interleukin-1TIRAP protein, humaninflammationinflammatory diseaseprotein-protein interaction (PPI)TIRAP (TIR domain-containing adaptor protein)TLR signaling

Identifiers

PMID34305934
PMCPMC8297548
OpenAlexW3181024808

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.