Evidence map›Paper›PMID 31720998›Full record

ArticleCell stress & chaperones2020

Response to oxidative stress of peripheral blood mononuclear cells from multiple sclerosis patients and healthy controls.

Cristiana Pistono, Maria Cristina Monti, Chiara Boiocchi, Francesca Gigli Berzolari, Cecilia Osera, Giulia Mallucci, Mariaclara Cuccia, Alessia Pascale, Cristina Montomoli, Roberto Bergamaschi

Open access · bronzeAbstract read
In one paragraph

Article in Cell stress & chaperones, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Oxidative Stress Markers in Multiple Sclerosis.International journal of molecular sciences · 2024
    Review
  6. Review
  7. Review
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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

10 authors at 2 institutions in 2 countries.

Cristiana PistonoLaboratory of Immunogenetics, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, Pavia, Italy. pistono@unistra.fr.ORCID 0000-0002-3304-0864
Maria Cristina MontiDepartment of Public Health Experimental and Forensic Medicine, Unit of Biostatistics and Clinical Epidemiology, University of Pavia, Pavia, Italy.
Chiara BoiocchiInter-Department Multiple Sclerosis Research Centre, National Neurological Institute "C. Mondino", Pavia, Italy.
Francesca Gigli BerzolariDepartment of Public Health Experimental and Forensic Medicine, Unit of Biostatistics and Clinical Epidemiology, University of Pavia, Pavia, Italy.
Cecilia OseraDepartment of Drug Sciences, Section of Pharmacology, University of Pavia, Pavia, Italy.
Giulia MallucciInter-Department Multiple Sclerosis Research Centre, National Neurological Institute "C. Mondino", Pavia, Italy.
Mariaclara CucciaLaboratory of Immunogenetics, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, Pavia, Italy.
Alessia PascaleDepartment of Drug Sciences, Section of Pharmacology, University of Pavia, Pavia, Italy.
Cristina MontomoliDepartment of Public Health Experimental and Forensic Medicine, Unit of Biostatistics and Clinical Epidemiology, University of Pavia, Pavia, Italy.
Roberto BergamaschiInter-Department Multiple Sclerosis Research Centre, National Neurological Institute "C. Mondino", Pavia, Italy.
University of Pavia · ITCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complex scenario of multiple sclerosis (MS) pathology involves several mechanisms, including oxidative stress response. The heat shock proteins (HSPs) are important for the protection of the cells; however, their role in MS is not clear. The present research is focused on the response of peripheral blood mononuclear cells (PBMCs) to oxidative stress and to the involvement of HSP70-2 (a protein coded by the HSPA1B gene, located in the MHC class III). To this aim, we challenged PBMCs from MS patients and healthy controls with hydrogen peroxide. Specifically, PBMCs mitochondrial activity, HSP70-2 protein expression and the production of intracellular reactive oxygen species were assessed. These parameters were also related to the HSP70-2 rs1061581 polymorphism, which is linked to the risk of developing MS. Moreover, mitochondrial activity and HSP70-2 protein levels were also related to disease severity. Overall, our results indicate that PBMCs, from both MS patients and healthy controls, may display a similar response towards an oxidative insult; within this context, HSP70-2 does not seem to be central in the protection of PBMCs. Nevertheless, the HSP70-2 rs1061581 polymorphism is related to ROS levels and appears to have a role in the different expression of HSP70-2 under oxidative stimulus.

Indexed as

AdultHeat-Shock ProteinsHumansLeukocytes, MononuclearMitochondriaMultiple SclerosisOxidative StressPolymorphism, GeneticReactive Oxygen SpeciesRNA, MessengerHeat-Shock ProteinsReactive Oxygen SpeciesRNA, MessengerHSP70-2Hydrogen peroxideMultiple sclerosisOxidative stressPBMCsrs1061581

Identifiers

PMID31720998
PMCPMC6985352
OpenAlexW2983389599

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.