Evidence map›Paper›PMID 34611893›Full record

Observational studyThe British journal of dermatology2021

Type I interferon response and vascular alteration in chilblain-like lesions during the COVID-19 outbreak.

L Frumholtz, J-D Bouaziz, M Battistella, J Hadjadj, R Chocron, D Bengoufa, H Le Buanec, L Barnabei, S Meynier, O Schwartz and 21 more

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in The British journal of dermatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
10.5field-weighted citation impact, top 1% 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, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Chilblains outbreak during COVID-19 pandemic: A Type-I interferonopathy?Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Pandemic chilblains: Are they SARS-CoV-2-related or not?Clinical immunology (Orlando, Fla.) · 2022
    Article
  19. Article
  20. Lack of association between pandemic chilblains and SARS-CoV-2 infection.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 4 institutions in 1 country.

L FrumholtzDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-3782-3890
J-D BouazizDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-4993-2461
M BattistellaUniversité de Paris, Human Immunology Pathophysiology Immunotherapy, INSERM U976, Institut de Recherche Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-7053-7431
J HadjadjUniversité de Paris, Imagine Institute, Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM U1163, F-75015, Paris, France.ORCID 0000-0002-2520-3272
R ChocronUniversité de Paris, PARCC, INSERM, F-75006, Paris, France.ORCID 0000-0002-5498-8937
D BengoufaImmunobiology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0003-1608-7510
H Le BuanecUniversité de Paris, Human Immunology Pathophysiology Immunotherapy, INSERM U976, Institut de Recherche Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-2139-0357
L BarnabeiUniversité de Paris, Imagine Institute, Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM U1163, F-75015, Paris, France.ORCID 0000-0001-9358-2633
S MeynierUniversité de Paris, Imagine Institute, Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM U1163, F-75015, Paris, France.ORCID 0000-0002-5675-4624
O SchwartzInstitut Pasteur, Virus and Immunity Unit, F-75015, Paris, France.ORCID 0000-0002-0729-1475
L GrzelakInstitut Pasteur, Virus and Immunity Unit, F-75015, Paris, France.ORCID 0000-0002-1298-7565
N SmithInstitut Pasteur, Translational Immunology Lab, F-75015, Paris, France.ORCID 0000-0002-0202-612X
B CharbitInstitut Pasteur, Cytometry and Biomarkers UTechS, CRT, F-75015, Paris, France.ORCID 0000-0002-5478-482X
D DuffyInstitut Pasteur, Translational Immunology Lab, F-75015, Paris, France.ORCID 0000-0002-8875-2308
N YatimDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0001-5326-1624
A CalugareanuDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0003-2841-1680
A PhilippeInstitut Pasteur, Cytometry and Biomarkers UTechS, CRT, F-75015, Paris, France.ORCID 0000-0003-3644-7464
C L GuerinUniversité de Paris, Innovative Therapies in Haemostasis, INSERM, F-75006, Paris, France.ORCID 0000-0002-1840-4017
B JolyBiological Haematology Department, AP-HP, Hôpital Lariboisière, F-75010, Paris, France.ORCID 0000-0003-0151-337X
V SiguretBiological Haematology Department, AP-HP, Hôpital Lariboisière, F-75010, Paris, France.ORCID 0000-0002-6509-8964
L JaumeDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-1968-0275
H BachelezDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-2845-4384
M BagotDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-1631-5192
F Rieux-LaucatUniversité de Paris, Imagine Institute, Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM U1163, F-75015, Paris, France.ORCID 0000-0001-7858-7866
S MaylinVirology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-0991-4381
J LegoffVirology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0001-7111-1865
C DelaugerreVirology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0001-6081-7993
N GendronUniversité de Paris, Innovative Therapies in Haemostasis, INSERM, F-75006, Paris, France.ORCID 0000-0003-4852-4738
D M SmadjaUniversité de Paris, Innovative Therapies in Haemostasis, INSERM, F-75006, Paris, France.ORCID 0000-0001-7731-9202
C CassiusDermatology Department, AP-HP, Hôpital Saint-Louis, F-75010, Paris, France.ORCID 0000-0002-5087-4414
Saint-Louis CORE (COvid REsearch)
Inserm · FRInstitut Pasteur · FRHôpital Saint-Louis · FRUniversité Paris Cité · FR

Funding

Agence Nationale de la Recherche AIROCovidAgence Nationale de la Recherche Investment for the FutureFondation Bettencourt SchuellerFondation pour la Recherche MédicaleFrench Friends of Sheba Tel Hashomer HospitalInstitut National de la Santé et de la Recherche Médicale
6 · The paper itself

Abstract

backgroundThe outbreak of chilblain-like lesions (CLL) during the COVID-19 pandemic has been reported extensively, potentially related to SARS-CoV-2 infection, yet its underlying pathophysiology is unclear.

objectivesTo study skin and blood endothelial and immune system activation in CLL in comparison with healthy controls and seasonal chilblains (SC), defined as cold-induced sporadic chilblains occurring during 2015 and 2019 with exclusion of chilblain lupus.

methodsThis observational study was conducted during 9-16 April 2020 at Saint-Louis Hospital, Paris, France. All patients referred with CLL seen during this period of the COVID-19 pandemic were included in this study. We excluded patients with a history of chilblains or chilblain lupus. Fifty patients were included.

resultsHistological patterns were similar and transcriptomic signatures overlapped in both the CLL and SC groups, with type I interferon polarization and a cytotoxic-natural killer gene signature. CLL were characterized by higher IgA tissue deposition and more significant transcriptomic activation of complement and angiogenesis factors compared with SC. We observed in CLL a systemic immune response associated with IgA antineutrophil cytoplasmic antibodies in 73% of patients, and elevated type I interferon blood signature in comparison with healthy controls. Finally, using blood biomarkers related to endothelial dysfunction and activation, and to angiogenesis or endothelial progenitor cell mobilization, we confirmed endothelial dysfunction in CLL.

conclusionsOur findings support an activation loop in the skin in CLL associated with endothelial alteration and immune infiltration of cytotoxic and type I IFN-polarized cells leading to clinical manifestations.

Indexed as

ChilblainsCOVID-19Interferon Type IFranceHumansPandemicsInterferon Type I

Identifiers

PMID34611893
PMCPMC8652826
OpenAlexW3202747215

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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.