Evidence map›Paper›PMID 32844538›Full record

ReviewReviews in medical virology2021

Alpha-1-antitrypsin: A possible host protective factor against Covid-19.

Mariana Braccialli de Loyola, Thaís Tereza Aguiar Dos Reis, Guilherme Xavier Lyra Malcher de Oliveira, Julys da Fonseca Palmeira, Gustavo A Argañaraz, Enrique R Argañaraz

Open access · bronzeAbstract readReview
In one paragraph

Review in Reviews in medical virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 10% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Severe COVID-19: Drugs and Clinical Trials.Journal of clinical medicine · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Small molecules in the treatment of COVID-19.Signal transduction and targeted therapy · 2022
    Review
  12. Sars-Cov2 Induced Biochemical Mechanisms in Liver Damage and Intestinal Lesions.Indian journal of clinical biochemistry : IJCB · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. SARS- CoV-2 infection and oxidative stress in early-onset preeclampsia.Biochimica et biophysica acta. Molecular basis of disease · 2022
    Review
  19. Review
  20. 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

6 authors at 1 institution in 1 country.

Mariana Braccialli de LoyolaLaboratory of Molecular Neurovirology, Faculty of Health Science, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-7816-764X
Thaís Tereza Aguiar Dos ReisLaboratory of Molecular Neurovirology, Faculty of Health Science, University of Brasília, Brasilia, Brazil.
Guilherme Xavier Lyra Malcher de OliveiraLaboratory of Molecular Neurovirology, Faculty of Health Science, University of Brasília, Brasilia, Brazil.
Julys da Fonseca PalmeiraLaboratory of Molecular Neurovirology, Faculty of Health Science, University of Brasília, Brasilia, Brazil.
Gustavo A ArgañarazLaboratory of Molecular Neurovirology, Faculty of Health Science, University of Brasília, Brasilia, Brazil.
Enrique R ArgañarazLaboratory of Molecular Neurovirology, Faculty of Health Science, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-4359-7594
Universidade de Brasília · BR

Funding

Fundação de Apoio à Pesquisa do Distrito Federal 0193001527/2016Fundação de Apoio à Pesquisa do Distrito Federal 0193001646/2017
6 · The paper itself

Abstract

Understanding Covid-19 pathophysiology is crucial for a better understanding of the disease and development of more effective treatments. Alpha-1-antitrypsin (A1AT) is a constitutive tissue protector with antiviral and anti-inflammatory properties. A1AT inhibits SARS-CoV-2 infection and two of the most important proteases in the pathophysiology of Covid-19: the transmembrane serine protease 2 (TMPRSS2) and the disintegrin and metalloproteinase 17 (ADAM17). It also inhibits the activity of inflammatory molecules, such as IL-8, TNF-α, and neutrophil elastase (NE). TMPRSS2 is essential for SARS-CoV-2-S protein priming and viral infection. ADAM17 mediates ACE2, IL-6R, and TNF-α shedding. ACE2 is the SARS-CoV-2 entry receptor and a key component for the balance of the renin-angiotensin system, inflammation, vascular permeability, and pulmonary homeostasis. In addition, clinical findings indicate that A1AT levels might be important in defining Covid-19 outcomes, potentially partially explaining associations with air pollution and with diabetes. In this review, we focused on the interplay between A1AT with TMPRSS2, ADAM17 and immune molecules, and the role of A1AT in the pathophysiology of Covid-19, opening new avenues for investigating effective treatments.

Indexed as

ADAM17 Proteinalpha 1-AntitrypsinAnimalsCOVID-19HumansProtective FactorsSerine EndopeptidasesADAM17 Proteinalpha 1-AntitrypsinSerine EndopeptidasesA1ATADAM17Covid-19SARS-CoV-2TMPRSS2

Identifiers

PMID32844538
PMCPMC7461031
OpenAlexW3080734665

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.