Evidence map›Paper›PMID 35093033›Full record

ReviewMolecular medicine (Cambridge, Mass.)2022

Immunometabolism in biofilm infection: lessons from cancer.

Rasoul Mirzaei, Niloofar Sabokroo, Yaghoub Ahmadyousefi, Hamid Motamedi, Sajad Karampoor

Open access · goldAbstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 55 citations in OpenAlex.

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  17. Extracellular Vesicles Derived FromJournal of parasitology research · 2024
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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

5 authors at 4 institutions in 1 country.

Rasoul MirzaeiDepartment of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. rasul.micro92@gmail.com.ORCID 0000-0002-4148-6495
Niloofar SabokrooDepartment of Microbiology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Yaghoub AhmadyousefiDepartment of Medical Biotechnology, School of Advanced Medical Sciences and Technologies, Hamadan University of Medical Sciences, Hamadan, Iran.
Hamid MotamediDepartment of Microbiology, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Sajad KarampoorGastrointestinal and Liver Diseases Research Center, Iran University of Medical Sciences, Tehran, Iran. sajadkarampour1987@gmail.com.
Hamedan University of Medical Sciences · IRIran University of Medical Sciences · IRKermanshah University of Medical Sciences · IRShahid Sadoughi University of Medical Sciences and Health Services · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiofilm is a community of bacteria embedded in an extracellular matrix, which can colonize different human cells and tissues and subvert the host immune reactions by preventing immune detection and polarizing the immune reactions towards an anti-inflammatory state, promoting the persistence of biofilm-embedded bacteria in the host. MAIN BODY OF THE MANUSCRIPT: It is now well established that the function of immune cells is ultimately mediated by cellular metabolism. The immune cells are stimulated to regulate their immune functions upon sensing danger signals. Recent studies have determined that immune cells often display distinct metabolic alterations that impair their immune responses when triggered. Such metabolic reprogramming and its physiological implications are well established in cancer situations. In bacterial infections, immuno-metabolic evaluations have primarily focused on macrophages and neutrophils in the planktonic growth mode.

conclusionBased on differences in inflammatory reactions of macrophages and neutrophils in planktonic- versus biofilm-associated bacterial infections, studies must also consider the metabolic functions of immune cells against biofilm infections. The profound characterization of the metabolic and immune cell reactions could offer exciting novel targets for antibiofilm therapy.

Indexed as

BiofilmsHost-Pathogen InteractionsAnimalsBiomarkersDisease ManagementDisease SusceptibilityEnergy MetabolismHumansImmune SystemInfectionsNeoplasmsOrgan SpecificityBiomarkersBiofilmBiofilm infectionCancerImmune polarizationImmunometabolismMetabolism

Identifiers

PMID35093033
PMCPMC8800364
OpenAlexW4210374470

What Socratic holds

Textmetadata
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 Socratic graph.