Evidence map›Paper›PMID 23974102›Full record

ArticleCell cycle (Georgetown, Tex.)2013

Metabolic profiling of human CD4+ cells following treatment with methotrexate and anti-TNF-α infliximab.

Maria Sole Chimenti, Paola Tucci, Eleonora Candi, Roberto Perricone, Gerry Melino, Anne E Willis

Open access · hybridAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
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  4. Endogenous drivers of altered immune cell metabolism.Experimental biology and medicine (Maywood, N.J.) · 2022
    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

6 authors at 5 institutions in 4 countries.

Maria Sole ChimentiRheumatology, Allergology and Clinical Immunology; Department of Internal Medicine; University of Rome Tor Vergata; Rome, Italy.
Paola Tucci
Eleonora Candi
Roberto Perricone
Gerry Melino
Anne E Willis
University of Rome Tor Vergata · ITCenter for Rheumatology · USMedical Research Council · GBNutrition Sciences (Belgium) · BEUniversity of Leicester · GB

Funding

Medical Research Council MC_U132670600Medical Research Council MC_UP_A600_1023
6 · The paper itself

Abstract

The autoimmune process in rheumatoid arthritis depends on activation of immune cells, which utilize intracellular kinases to respond to external stimuli such as cytokines, immune complexes, and antigens. CD4+ T cells comprise a large proportion of the inflammatory cells that invade the synovial tissue and may therefore be a cell type of pathogenic importance. Both methotrexate and infliximab are effective in the treatment of inflammatory arthritis; however, the biological effects triggered by these treatments and the biochemical mechanisms underlining the cell response are still not fully understood. Thus, in this study the global metabolic changes associated with methotrexate or infliximab treatment of isolated human CD4+ T cells were examined using gas chromatography/mass spectrometry or liquid chromatography/mass spectrometry. In total 148 metabolites involved in selective pathways were found to be significantly altered. Overall, the changes observed are likely to reflect the effort of CD4+ cells to increase the production of cellular reducing power to offset the cellular stress exerted by treatment. Importantly, analysis of the global metabolic changes associated with MTX or infliximab treatment of isolated human CD4+ T cells suggested that the toxicity associated with these agents is minimal when used at clinically relevant concentrations.

Indexed as

Antibodies, MonoclonalAnti-Inflammatory Agents, Non-SteroidalAntimetabolites, AntineoplasticArthritis, RheumatoidCD4-Positive T-LymphocytesCells, CulturedChromatography, High Pressure LiquidGas Chromatography-Mass SpectrometryGlycogenHumansInfliximabMass SpectrometryMetabolomeMethotrexateTumor Necrosis Factor-alphaAntibodies, MonoclonalAnti-Inflammatory Agents, Non-SteroidalAntimetabolites, AntineoplasticGlycogenInfliximabMethotrexateTumor Necrosis Factor-alphaapoptosisautoimmunity diseaserheumatoid arthritisT cells

Identifiers

PMID23974102
PMCPMC3875677
OpenAlexW1972749396

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.