Evidence map›Paper›PMID 33424861›Full record

ArticleFrontiers in immunology2020

Modeling MyD88 Deficiency

Nils Craig-Mueller, Ruba Hammad, Roland Elling, Jamal Alzubi, Barbara Timm, Julia Kolter, Nele Knelangen, Christien Bednarski, Birgitta Gläser, Sandra Ammann and 9 more

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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  9. [Effect ofSichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2023
    Article
  10. Frontiers in immunology · 2022
    Review
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

19 authors at 5 institutions in 1 country.

Nils Craig-MuellerInstitute for Transfusion Medicine and Gene Therapy, Medical Center-University of Freiburg, Freiburg, Germany.
Ruba HammadInstitute for Transfusion Medicine and Gene Therapy, Medical Center-University of Freiburg, Freiburg, Germany.
Roland EllingCenter for Chronic Immunodeficiency (CCI), Medical Center-University of Freiburg, Freiburg, Germany.
Jamal AlzubiInstitute for Transfusion Medicine and Gene Therapy, Medical Center-University of Freiburg, Freiburg, Germany.
Barbara TimmInstitute for Transfusion Medicine and Gene Therapy, Medical Center-University of Freiburg, Freiburg, Germany.
Julia KolterCenter for Chronic Immunodeficiency (CCI), Medical Center-University of Freiburg, Freiburg, Germany.
Nele KnelangenCenter for Chronic Immunodeficiency (CCI), Medical Center-University of Freiburg, Freiburg, Germany.
Christien BednarskiInstitute for Transfusion Medicine and Gene Therapy, Medical Center-University of Freiburg, Freiburg, Germany.
Birgitta GläserInstitute of Human Genetics, Medical Center-University of Freiburg, Freiburg, Germany.
Sandra AmmannCenter for Chronic Immunodeficiency (CCI), Medical Center-University of Freiburg, Freiburg, Germany.
Zoltán IvicsDivision of Medical Biotechnology, Paul-Ehrlich Institute, Langen, Germany.
Judith FischerInstitute of Human Genetics, Medical Center-University of Freiburg, Freiburg, Germany.
Carsten SpeckmannCenter for Chronic Immunodeficiency (CCI), Medical Center-University of Freiburg, Freiburg, Germany.
Klaus SchwarzInstitute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Service Baden-Württemberg-Hessen, and Institute for Transfusion Medicine, University of Ulm, Ulm, Germany.
Nico LachmannInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Stephan EhlCenter for Chronic Immunodeficiency (CCI), Medical Center-University of Freiburg, Freiburg, Germany.
Thomas MoritzInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Philipp HennekeCenter for Chronic Immunodeficiency (CCI), Medical Center-University of Freiburg, Freiburg, Germany.
Toni CathomenInstitute for Transfusion Medicine and Gene Therapy, Medical Center-University of Freiburg, Freiburg, Germany.
University Medical Center Freiburg · DEUniversity of Freiburg · DEMedizinische Hochschule Hannover · DEPaul Ehrlich Institut · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited defects in MyD88 and IRAK4, two regulators in Toll-like receptor (TLR) signaling, are clinically highly relevant, but still incompletely understood. MyD88- and IRAK4-deficient patients are exceedingly susceptible to a narrow spectrum of pathogens, with ∼50% lethality in the first years of life. To better understand the underlying molecular and cellular characteristics that determine disease progression, we aimed at modeling the cellular response to pathogens

Indexed as

Cell DifferentiationCell LineCytokinesHEK293 CellsHumansInduced Pluripotent Stem CellsInterleukin-1 Receptor-Associated KinasesMacrophagesMonocytesMyeloid CellsMyeloid Differentiation Factor 88Primary Immunodeficiency DiseasesSignal TransductionCytokinesInterleukin-1 Receptor-Associated KinasesMYD88 protein, humanMyeloid Differentiation Factor 88cell therapygene therapyiMacinduced pluripotent stem cells (iPSC)IRAK4MyD88Toll-like receptortransposon

Identifiers

PMID33424861
PMCPMC7786022
OpenAlexW3114189267

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.