Evidence map›Paper›PMID 35640018›Full record

ArticleThe Journal of experimental medicine2022

Chemokines form nanoparticles with DNA and can superinduce TLR-driven immune inflammation.

Yong Du, Marie Dominique Ah Kioon, Paoline Laurent, Vidyanath Chaudhary, Michael Pierides, Chao Yang, David Oliver, Lionel B Ivashkiv, Franck J Barrat

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  4. The immunoproteasome regulates ILC2 responses by modulating mitochondrial capacity.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  13. Inhibiting the P2YJACC. Basic to translational science · 2024
    Article
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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

9 authors at 1 institution in 1 country.

Yong DuHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0003-2986-6249
Marie Dominique Ah KioonHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0003-2319-0444
Paoline LaurentHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0001-7102-2184
Vidyanath ChaudharyHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0002-6000-7517
Michael PieridesHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0002-7882-6967
Chao YangHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0002-8661-3275
David OliverHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0002-2034-0921
Lionel B IvashkivHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0002-9951-0646
Franck J BarratHSS Research Institute, Hospital for Special Surgery, New York, NY.ORCID 0000-0002-0735-0850
Hospital for Special Surgery · US

Funding

STEROID THERAPY AND CYTOKINES IN RHEUMATIC DISEASESR01AI046712 · NIAID · HOSPITAL FOR SPECIAL SURGERY · PI IVASHKIV, LIONEL B · 2000 to 2025
$12.5M
Fc Receptors &Cytokine Balance in Rheumatoid ArthritisR01AR050401 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI Lionel B Ivashkiv · 2004 to 2026
$7.4M
Role of plasmacytoid dendritic cells in autoimmunityR01AI132447 · NIAID · HOSPITAL FOR SPECIAL SURGERY · PI BARRAT, FRANCK · 2018 to 2022
$2.2M
National Scleroderma FoundationNIAID NIH HHS R01 AI046712NIAID NIH HHS R01 AI132447NIAMS NIH HHS R01 AR050401NIH HHS 1R01AI132447Scleroderma Research FoundationTow Foundation
6 · The paper itself

Abstract

Chemokines control the migratory patterns and positioning of immune cells to organize immune responses to pathogens. However, many chemokines have been associated with systemic autoimmune diseases that have chronic IFN signatures. We report that a series of chemokines, including CXCL4, CXCL10, CXCL12, and CCL5, can superinduce type I IFN (IFN-I) by TLR9-activated plasmacytoid DCs (pDCs), independently of their respective known chemokine receptors. Mechanistically, we show that chemokines such as CXCL4 mediate transcriptional and epigenetic changes in pDCs, mostly targeted to the IFN-I pathways. We describe that chemokines physically interact with DNA to form nanoparticles that promote clathrin-mediated cellular uptake and delivery of DNA in the early endosomes of pDCs. Using two separate mouse models of skin inflammation, we observed the presence of CXCL4 associated with DNA in vivo. These data reveal a noncanonical role for chemokines to serve as nucleic acid delivery vectors to modulate TLR signaling, with implications for the chronic presence of IFN-I by pDCs in autoimmune diseases.

Indexed as

ChemokinesDendritic CellsNanoparticlesToll-Like ReceptorsAnimalsDNAInflammationMiceChemokinesDNAToll-Like Receptors

Identifiers

PMID35640018
PMCPMC9161158
OpenAlexW4282936101

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.