Evidence map›Paper›PMID 33221483›Full record

ArticleTranslational research : the journal of laboratory and clinical medicine2021

The role of the lectin pathway of the complement system in SARS-CoV-2 lung injury.

Mineia Alessandra Scaranello Malaquias, Ana Carolina Gadotti, Jarbas da Silva Motta-Junior, Ana Paula Camargo Martins, Marina Luise Viola Azevedo, Ana Paula Kubaski Benevides, Plínio Cézar-Neto, Letícia Arianne Panini do Carmo, Rafaela Chiuco Zeni, Sonia Mara Raboni and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Translational research : the journal of laboratory and clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 15% 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

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

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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

14 authors at 2 institutions in 1 country.

Mineia Alessandra Scaranello MalaquiasPostdoctoral Researcher Postgraduate Program in Health Sciences School of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil. Electronic address: andrea.moreno@pucpr.br.
Ana Carolina GadottiPostgraduate Program of Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Jarbas da Silva Motta-JuniorPostgraduate Program of Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Ana Paula Camargo MartinsLaboratory of Experimental Pathology, School of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Marina Luise Viola AzevedoLaboratory of Experimental Pathology, School of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Ana Paula Kubaski BenevidesLaboratory of Experimental Pathology, School of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Plínio Cézar-NetoSchool of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Letícia Arianne Panini do CarmoSchool of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Rafaela Chiuco ZeniSchool of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Sonia Mara RaboniLaboratory of Virology, Hospital de Clínicas, Federal University of Paraná - UFPR, Curitiba, PR, Brazil.
Aline Simoneti FonsecaFaculdades Pequeno Príncipe (FPP). Instituto de Pesquisa Pelé Pequeno Príncipe (IPPPP), Curitiba, PR, Brazil.
Cleber Machado-SouzaFaculdades Pequeno Príncipe (FPP). Instituto de Pesquisa Pelé Pequeno Príncipe (IPPPP), Curitiba, PR, Brazil.
Andrea Novais Moreno-AmaralAnemia and Immunology Research Laboratory (LabAIRe), School of Medicine, Pontifical Catholic University of Parana - PUCPR, Curitiba, PR, Brazil.
Lucia de NoronhaLaboratory of Experimental Pathology, School of Medicine, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, PR, Brazil.
Pontifícia Universidade Católica do Paraná · BRUniversidade Federal do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although some evidence showed the activation of complement systems in COVID-19 patients, proinflammatory status and lectin pathway remain unclear. Thus, the present study aimed to demonstrate the role of MBL and ficolin-3 in the complement system activation and compared to pandemic Influenza A virus H1N1 subtype infection (H1N1pdm09) and control patients. A total of 27 lungs formalin-fixed paraffin-embedded samples (10 from H1N1 group, 6 from the COVID-19 group, and 11 from the control group) were analyzed by immunohistochemistry using anti-IL-6, TNF-alfa, CD163, MBL e FCN3 antibodies. Genotyping of target polymorphisms in the MBL2 gene was performed by real-time PCR. Proinflammatory cytokines such as IL-6 and TNF-alpha presented higher tissue expression in the COVID-19 group compared to H1N1 and control groups. The same results were observed for ICAM-1 tissue expression. Increased expression of the FCN3 was observed in the COVID-19 group and H1N1 group compared to the control group. The MBL tissue expression was higher in the COVID-19 group compared to H1N1 and control groups. The genotypes AA for rs180040 (G/A), GG for rs1800451 (G/A) and CC for rs5030737 (T/C) showed a higher prevalence in the COVID-19 group. The intense activation of the lectin pathway, with particular emphasis on the MBL pathway, together with endothelial dysfunction and a massive proinflammatory cytokines production, possibly lead to a worse outcome in patients infected with SARS-Cov-2. Moreover, 3 SNPs of our study presented genotypes that might be correlated with high MBL tissue expression in the COVID-19 pulmonary samples.

Indexed as

SARS-CoV-2AdultAgedAged, 80 and overAutopsyCase-Control StudiesComplement ActivationCOVID-19CytokinesFemaleGenotypeHumansImmunohistochemistryInfluenza A Virus, H1N1 SubtypeInfluenza, HumanLectinsCytokinesLectins

Identifiers

PMID33221483
PMCPMC7677075
OpenAlexW3109446887

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.