Evidence map›Paper›PMID 35249135›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2022

High levels of extracellular ATP lead to different inflammatory responses in COVID-19 patients according to the severity.

Gilnei Bruno da Silva, Daiane Manica, Alana Patrícia da Silva, Greicy Cristine Kosvoski, Marceli Hanauer, Charles Elias Assmann, Júlia Leão Batista Simões, Micheli Mainardi Pillat, Jéssica Dotto de Lara, Filomena Marafon and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
6.3field-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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Dynamic metabolic modelling of ATP allocation during viral infection.Journal of the Royal Society, Interface · 2026
    Article
  4. Article
  5. Review
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  16. Time-resolved role of P2X4 and P2X7 during CD8Frontiers in immunology · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. Purinergic signaling pathway in severe COVID-19.Current opinion in pharmacology · 2023
    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

17 authors at 3 institutions in 1 country.

Gilnei Bruno da Silva *Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.ORCID 0000-0002-1908-123X
Daiane Manica *Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.ORCID 0000-0003-3126-954X
Alana Patrícia da SilvaGraduate Program in Science and Food Technology, Federal University of Fronteira Sul, Laranjeiras Do Sul, PR, Brazil.ORCID 0000-0002-4710-8516
Greicy Cristine KosvoskiGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.ORCID 0000-0002-3400-446X
Marceli HanauerGraduate Program in Nursing, Federal University of Santa Catarina, Florianópolis, SC, Brazil.ORCID 0000-0002-5798-2709
Charles Elias AssmannGraduate Program in Biological Sciences: Toxicological Biochemistry, Department of Biochemistry and Molecular Biology, Federal University of Santa Maria, Santa Maria, RS, Brazil.ORCID 0000-0002-3524-3446
Júlia Leão Batista SimõesGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.ORCID 0000-0002-1652-9692
Micheli Mainardi PillatGraduate Program in Pharmaceutical Sciences, Department of Microbiology and Parasitology, Federal University of Santa Maria, Santa Maria, RS, Brazil.ORCID 0000-0002-6753-6083
Jéssica Dotto de LaraGraduate Program in Pharmaceutical Sciences, Department of Microbiology and Parasitology, Federal University of Santa Maria, Santa Maria, RS, Brazil.ORCID 0000-0002-7204-7196
Filomena MarafonGraduate Program in Biochemistry, Department of Biological Science, Federal University of Santa Catarina, Florianópolis, SC, Brazil.ORCID 0000-0001-9167-0146
Amanda Gollo BertolloGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.
Maiqueli E D MingotiGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.ORCID 0000-0002-7462-3425
Jullye GavioliGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.
Gislaine Zilli RéusGraduate Program in Health Sciences, Department of Translational Psychiatry, University of the Extreme South of Santa Catarina, SC, Criciúma, Brazil.ORCID 0000-0001-6073-0855
Gabriela Gonçalves de OliveiraGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.
Zuleide Maria IgnácioGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.ORCID 0000-0002-1417-1308
Margarete Dulce BagatiniGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil. margaretebagatini@yahoo.com.br.ORCID 0000-0001-9263-4980
Universidade Federal da Fronteira Sul · BRUniversidade Federal de Santa Maria · BRUniversidade Federal de Santa Catarina · BR

Funding

CNPq 404256/2021-0
6 · The paper itself

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has significantly impacted the world and has driven many researchers into the pathophysiology of COVID-19. In the findings, there is a close association between purinergic signaling and the immune response. Then, this study aimed to evaluate alterations in the purinergic signaling in COVID-19 patients according to range severity. We divided the COVID-19 patients into moderate and severe cases following the guideless of NIH and WHO, together with clinical characteristics. The blood samples were collected to obtain PBMCs and platelets. We analyzed the ectonucleotidase activities through ATP, ADP, AMP, Ado hydrolysis, E-NTPDase1 (CD39), and 5'-NT (CD73) expression by flow cytometry in total leukocytes. The extracellular ATP was measured by bioluminescence, and cytokines were analyzed by flow cytometry. We observed a decrease in ATP hydrolysis and increased AMP hydrolysis in PBMCs for both groups. In severe cases, ATP hydrolysis was raised for the platelets, while ADP and AMP hydrolysis have risen significantly in both groups. Additionally, there was a significant increase in ADP hydrolysis in severe cases compared to moderate cases. In addition, we observed an increase in the ADA activity in platelets of moderate patients. Moderate and severe cases showed increased expression of CD39 and CD73 in total leukocytes. To finalize the purinergic signaling, extracellular ATP was increased in both groups. Furthermore, there was an increase in IL-2, IL-6, IL-10, and IL-17 in moderate and severe groups. Thus, for the first time, our findings confirm the changes in purinergic signaling and immune response in COVID-19, in addition to making it more evident that the severity range directly impacts these changes. Therefore, the therapeutic potential of the purinergic system must be highlighted and studied as a possible target for the treatment of SARS-CoV-2 disease. KEY MESSAGES: COVID-19 patients exhibit alterations in purinergic system and immune response. High levels of extracellular ATP lead to different inflammatory responses. CD39 and CD73 expression were increased in COVID-19 patients. Cytokines IL-2, IL-6, IL-10, and IL-17 also were altered in these patients. The purinergic system may be a possibility target to SARS-CoV-2 treatments.

Indexed as

COVID-19Adenosine TriphosphateBlood PlateletsHumansPandemicsSARS-CoV-2Adenosine TriphosphateCOVID-19EctonucleotidaseImmune systemPurinergic system

Identifiers

PMID35249135
PMCPMC8898096
OpenAlexW4220817778

What Socratic 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 Socratic graph.