Evidence map›Paper›PMID 34764281›Full record

ArticleNature communications2021

Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy.

Matthias Kettwig, Katharina Ternka, Kristin Wendland, Dennis Manfred Krüger, Silvia Zampar, Charlotte Schob, Jonas Franz, Abhishek Aich, Anne Winkler, M Sadman Sakib and 18 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.8field-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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  14. RNase T2 restricts TLR13-mediated autoinflammation in vivo.The Journal of experimental medicine · 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

28 authors at 7 institutions in 3 countries.

Matthias Kettwig *Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany. matthias.kettwig@med.uni-goettingen.de.ORCID http://orcid.org/0000-0003-4804-7716
Katharina Ternka *Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.ORCID http://orcid.org/0000-0003-3773-4625
Kristin WendlandDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Dennis Manfred KrügerDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Silvia ZamparDepartment of Psychiatry and Psychotherapy, University Medical Center Göttingen, Georg August University, Göttingen, Germany.ORCID http://orcid.org/0000-0003-0134-0974
Charlotte SchobDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Jonas FranzInstitute of Neuropathology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.ORCID http://orcid.org/0000-0001-7523-6622
Abhishek AichDepartment of Cellular Biochemistry, University Medical Center Göttingen, Georg August University, Göttingen, Germany.ORCID http://orcid.org/0000-0001-8331-9874
Anne WinklerInstitute of Neuropathology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
M Sadman SakibDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Lalit KauraniDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Robert EppleDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Hauke B WernerDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.ORCID http://orcid.org/0000-0002-7710-5738
Samy HakroushInstitute of Pathology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Julia KitzInstitute of Pathology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Marco PrinzInstitute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-0349-1955
Eva BartokInstitute of Clinical Chemistry and Clinical Pharmacology, University Hospital, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0003-0556-1950
Gunther HartmannInstitute of Clinical Chemistry and Clinical Pharmacology, University Hospital, University of Bonn, Bonn, Germany.
Simone SchröderDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Peter RehlingDepartment of Cellular Biochemistry, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Marco HennekeDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Susann BoretiusFunctional Imaging Laboratory, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.ORCID http://orcid.org/0000-0003-2792-7423
A AliaInstitute for Medical Physics and Biophysics, University of Leipzig, Leipzig, Germany.
Oliver WirthsDepartment of Psychiatry and Psychotherapy, University Medical Center Göttingen, Georg August University, Göttingen, Germany.ORCID http://orcid.org/0000-0002-4115-0334
Andre FischerDepartment for Epigenetics and Systems Medicine in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Christine StadelmannInstitute of Neuropathology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.ORCID http://orcid.org/0000-0003-1766-5458
Stefan NesslerInstitute of Neuropathology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Jutta GärtnerDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.
Universitätsmedizin Göttingen · DEGerman Center for Neurodegenerative Diseases · DEUniversity of Bonn · DEGerman Primate Center · DELeiden University · NLMax Planck Institute of Experimental Medicine · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infantile-onset RNaseT2 deficient leukoencephalopathy is characterised by cystic brain lesions, multifocal white matter alterations, cerebral atrophy, and severe psychomotor impairment. The phenotype is similar to congenital cytomegalovirus brain infection and overlaps with type I interferonopathies, suggesting a role for innate immunity in its pathophysiology. To date, pathophysiological studies have been hindered by the lack of mouse models recapitulating the neuroinflammatory encephalopathy found in patients. In this study, we generated Rnaset2

Indexed as

AnimalsCD8-Positive T-LymphocytesCognitive DysfunctionDisease Models, AnimalEndoribonucleasesFemaleFlow CytometryGenotypeHumansImmunohistochemistryLeukoencephalopathiesMagnetic Resonance ImagingMaleMemory T CellsMiceMice, KnockoutEndoribonucleases

Identifiers

PMID34764281
PMCPMC8586222
OpenAlexW3211905208

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.