Evidence map›Paper›PMID 32656939›Full record

ReviewReviews in medical virology2020

Lessons from dermatology about inflammatory responses in Covid-19.

Paulo Ricardo Criado, Carla Pagliari, Francisca Regina Oliveira Carneiro, Juarez Antonio Simões Quaresma

Open access · bronzeAbstract readReview
In one paragraph

Review in Reviews in medical virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

19 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Cutaneous Manifestations of Coronavirus Disease 2019: Skin Narratives and Dialogues.The Journal of clinical and aesthetic dermatology · 2022
    Article
  3. Article
  4. Observational
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Serological cross-reaction and coinfection of dengue and COVID-19 in Asia: Experience from Indonesia.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Article
  13. Projected supportive effects of PycnogenolInternational journal of antimicrobial agents · 2020
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

4 authors at 3 institutions in 1 country.

Paulo Ricardo CriadoDermatology Department, Centro Universitário Saúde ABC, Santo André, Brazil.ORCID https://orcid.org/0000-0001-9785-6099
Carla PagliariPathology Department, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-6210-6917
Francisca Regina Oliveira CarneiroCenter of Biological and Health Sciences, State University of Pará, Belém, Brazil.
Juarez Antonio Simões QuaresmaCenter of Biological and Health Sciences, State University of Pará, Belém, Brazil.ORCID https://orcid.org/0000-0002-6267-9966
Universidade do Estado do Pará · BRFaculdade de Medicina do ABC · BRHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-Cov-2 is a single-stranded RNA virus composed of 16 non-structural proteins (NSP 1-16) with specific roles in the replication of coronaviruses. NSP3 has the property to block host innate immune response and to promote cytokine expression. NSP5 can inhibit interferon (IFN) signalling and NSP16 prevents MAD5 recognition, depressing the innate immunity. Dendritic cells, monocytes, and macrophages are the first cell lineage against viruses' infections. The IFN type I is the danger signal for the human body during this clinical setting. Protective immune responses to viral infection are initiated by innate immune sensors that survey extracellular and intracellular space for foreign nucleic acids. In Covid-19 the pathogenesis is not yet fully understood, but viral and host factors seem to play a key role. Important points in severe Covid-19 are characterized by an upregulated innate immune response, hypercoagulopathy state, pulmonary tissue damage, neurological and/or gastrointestinal tract involvement, and fatal outcome in severe cases of macrophage activation syndrome, which produce a 'cytokine storm'. These systemic conditions share polymorphous cutaneous lesions where innate immune system is involved in the histopathological findings with acute respiratory distress syndrome, hypercoagulability, hyperferritinemia, increased serum levels of D-dimer, lactic dehydrogenase, reactive-C-protein and serum A amyloid. It is described that several polymorphous cutaneous lesions similar to erythema pernio, urticarial rashes, diffuse or disseminated erythema, livedo racemosa, blue toe syndrome, retiform purpura, vesicles lesions, and purpuric exanthema or exanthema with clinical aspects of symmetrical drug-related intertriginous and flexural exanthema. This review describes the complexity of Covid-19, its pathophysiological and clinical aspects.

Indexed as

Angiotensin-Converting Enzyme 2BetacoronavirusCoronavirus InfectionsCOVID-19Cytokine Release SyndromeDisease ProgressionDisseminated Intravascular CoagulationErythemaExanthemaGene Expression RegulationHost-Pathogen InteractionsHumansImmunity, InnateLymphocytesMacrophagesPandemicsACE2 protein, humanAngiotensin-Converting Enzyme 2Peptidyl-Dipeptidase AReceptors, VirusSerine EndopeptidasesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2TMPRSS2 protein, humanCovid-19innate immunitylipoprotein alivedoid vasculitisSARS-CoV-2skin

Identifiers

PMID32656939
PMCPMC7404593
OpenAlexW3041715746

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.