Evidence map›Paper›PMID 30349535›Full record

ArticleFrontiers in immunology2018

Ficolin-1 and Ficolin-3 Plasma Levels Are Altered in HIV and HIV/HCV Coinfected Patients From Southern Brazil.

Maria Regina Tizzot, Kárita Cláudia Freitas Lidani, Fabiana Antunes Andrade, Hellen Weinschutz Mendes, Marcia Holsbach Beltrame, Edna Reiche, Steffen Thiel, Jens C Jensenius, Iara J de Messias-Reason

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Ficolin-1 in pediatricInfection and immunity · 2025
    Article
  2. Article
  3. Article
  4. Deimination Protein Profiles inFrontiers in immunology · 2020
    Article
  5. Article
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

9 authors at 2 institutions in 2 countries.

Maria Regina TizzotLaboratory of Molecular Immunopathology, Department of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Kárita Cláudia Freitas LidaniLaboratory of Molecular Immunopathology, Department of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Fabiana Antunes AndradeLaboratory of Molecular Immunopathology, Department of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Hellen Weinschutz MendesLaboratory of Molecular Immunopathology, Department of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Marcia Holsbach BeltrameLaboratory of Molecular Immunopathology, Department of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Edna ReicheClinic Hospital, Estate University of Londrina, Londrina, Brazil.
Steffen ThielDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Jens C JenseniusDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Iara J de Messias-ReasonLaboratory of Molecular Immunopathology, Department of Medical Pathology, Federal University of Paraná, Curitiba, Brazil.
Universidade Federal do Paraná · BRAarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complement system is a key component of the innate immune system, participating in the surveillance against infectious agents. Once activated by one of the three different pathways, complement mediates cell lysis, opsonization, signalizes pathogens for phagocytosis and induces the adaptive immune response. The lectin pathway is constituted by several soluble and membrane bound proteins, called pattern recognition molecules (PRM), including mannose binding lectin (MBL), Ficolins-1, -2, and -3, and Collectin 11. These PRMs act on complement activation as recognition molecules of pathogen-associated molecular patterns (PAMPs) such as N-acetylated, found in glycoproteins of viral envelopes. In this study, Ficolin-1 and Ficolin-3 plasma levels were evaluated in 178 HIV patients (93 HIV; 85 HIV/HCV) and 85 controls from southern Brazil. Demographic and clinical-laboratory findings were obtained during medical interview and from medical records. All parameters were assessed by logistic regression, adjusted for age, ancestry, and sex. Significantly lower levels of Ficolin-1 were observed in HIV/HCV coinfected when compared to HIV patients (

Indexed as

AdultAgedBrazilCoinfectionFemaleFicolinsGlycoproteinsHepatitis CHIV InfectionsHumansLectinsMaleMiddle AgedFCN3 protein, humanFicolinsGlycoproteinsLectinscomplement systemFicolin-1Ficolin-3hepatitis C virusHIV infection

Identifiers

PMID30349535
PMCPMC6187973
OpenAlexW2897829536

What OpenQuestion holds

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LicenceCC BY
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.