Evidence map›Paper›PMID 32313246›Full record

ArticleNature immunology2020

Cxcl10

Amir Giladi, Lisa Katharina Wagner, Hanjie Li, Dorothea Dörr, Chiara Medaglia, Franziska Paul, Anat Shemer, Steffen Jung, Simon Yona, Matthias Mack and 3 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
7.1field-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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Expanding roles of cGAS-STING signaling in neuroinflammation.The Journal of clinical investigation · 2026
    Review
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12 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Amir Giladi *Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0000-0002-5880-2845
Lisa Katharina Wagner *Max-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.
Hanjie LiDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Dorothea DörrMax-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.
Chiara MedagliaDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Franziska PaulDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Anat ShemerDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Steffen JungDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0000-0003-4290-5716
Simon YonaFaculty of Dental Medicine, Hebrew University, Jerusalem, Israel.
Matthias MackDepartment of Nephrology, Universitätsklinikum Regensburg, Regensburg, Germany.
Achim LeutzMax-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.ORCID http://orcid.org/0000-0001-8259-927X
Ido AmitDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel. ido.amit@weizmann.ac.il.ORCID http://orcid.org/0000-0003-2968-877X
Alexander MildnerMax-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany. alexander.mildner@mdc-berlin.de.ORCID http://orcid.org/0000-0002-2019-8427
Weizmann Institute of Science · ILMax Delbrück Center · DEHebrew University of Jerusalem · ILUniversity Hospital Regensburg · DE

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Multiple sclerosis (MS) is characterized by pathological inflammation that results from the recruitment of lymphoid and myeloid immune cells from the blood into the brain. Due to subset heterogeneity, defining the functional roles of the various cell subsets in acute and chronic stages of MS has been challenging. Here, we used index and transcriptional single-cell sorting to characterize the mononuclear phagocytes that infiltrate the central nervous system from the periphery in mice with experimentally induced autoimmune encephalomyelitis, a model of MS. We identified eight monocyte and three dendritic cell subsets at acute and chronic disease stages in which the defined transcriptional programs pointed toward distinct functions. Monocyte-specific cell ablation identified Cxcl10

Indexed as

AnimalsAutoimmunityCell DifferentiationCells, CulturedCentral Nervous SystemChemokine CXCL10Dendritic CellsEncephalomyelitis, Autoimmune, ExperimentalFemaleHumansMiceMice, Inbred C57BLMice, TransgenicMonocytesMultiple SclerosisNeurogenic InflammationChemokine CXCL10Saa3 protein, mouseSerum Amyloid A ProteinTranscription FactorsZbtb46 protein, mouse

Identifiers

PMID32313246
OpenAlexW3016532619

What OpenQuestion holds

Textmetadata
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.