Evidence map›Paper›PMID 39775542›Full record

ArticlePloS one2024

Evaluation of the effect of cell freshness on pyrogen detection using a serum-free monocyte-activation test.

Katsuhiko Hayashi, Mizuki Sano, Toshie Kanayasu-Toyoda, Yuji Morita, Teruhide Yamaguchi, Kenji Ohya, Yutaka Kikuchi, Ken-Ichi Izutsu, Yukiko Hara-Kudo

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Katsuhiko HayashiDivision of Microbiology, National Institute of Health Sciences, Kawasaki, Kanagawa, Japan.ORCID 0000-0001-7359-5939
Mizuki SanoDepartment of Infection Control Science, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Toshie Kanayasu-ToyodaDepartment of Pharmaceutical and Medical Business Sciences, Nihon Pharmaceutical University, Kitaadachi-gun, Saitama, Japan.
Yuji MoritaDepartment of Infection Control Science, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Teruhide YamaguchiDepartment of Pharmaceutical and Medical Business Sciences, Nihon Pharmaceutical University, Kitaadachi-gun, Saitama, Japan.
Kenji OhyaDivision of Microbiology, National Institute of Health Sciences, Kawasaki, Kanagawa, Japan.
Yutaka KikuchiDepartment of Nutrition, Faculty of Healthcare Sciences, Chiba Prefectural University of Health Sciences, Chiba, Japan.
Ken-Ichi IzutsuDepartment of Pharmaceutical Sciences, School of Pharmacy International University of Health and Welfare, Ohtawara, Tochigi, Japan.
Yukiko Hara-KudoDivision of Microbiology, National Institute of Health Sciences, Kawasaki, Kanagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pyrogens cause shock symptoms when released into the bloodstream. They are classified into two main categories: endotoxins (lipopolysaccharides [LPS]) and non-endotoxin pyrogens. The monocyte activation test (MAT) is an in vitro assay to detect pyrogens in human monocytes. Cells were incubated in the culture medium, and the cellular response, specifically the production of the inflammatory cytokine interleukin-6 in the culture supernatant, was analyzed using enzyme-linked immunosorbent assay (ELISA). Technical improvements, such as cell acquisition and culture media selection, will be beneficial for the popularization of MAT. The cell freshness was strictly controlled to achieve high MAT sensitivity. However, it is necessary to investigate the usability of older and stored blood samples in the MAT. This study evaluated the effect of cell freshness on MAT using peripheral blood mononuclear cells (PBMCs) isolated from 2- and 5-d-old donated whole blood samples. To mitigate the influence of serum in the culture medium, a serum-free MAT was developed using the LPS-binding protein (LBP) as an enhancer for LPS detection. PBMCs were incubated with a two-fold dilution series of LPS at 0.001-4.096 endotoxin units/mL (EU/mL). Interleukin-6 levels in the culture supernatant were quantified by ELISA in the presence and absence of LBP. In the presence of LBP, the limit of detection (LOD) for LPS was 0.001-0.008 EU/mL. However, in the absence of LBP, the LOD was 0.512 EU/mL. Peripheral PBMCs were 38.6 times more sensitive in the presence of LBP than in its absence. When utilizing the developed serum-free MAT with LBP, 5-d-old PBMCs showed LODs of 0.016-0.064 EU/mL, indicating a 3.1-fold increase in sensitivity compared with 5- to 2-d-old PBMCs. These results suggest that the sensitivity of PBMCs decreased gradually rather than sharply. The study concluded that 2-d-old PBMCs were sufficiently fresh and could be used as serum-free MAT.

Indexed as

Enzyme-Linked Immunosorbent AssayInterleukin-6LipopolysaccharidesMonocytesPyrogensAcute-Phase ProteinsCarrier ProteinsCells, CulturedCulture Media, Serum-FreeHumansLeukocytes, MononuclearLipopolysaccharide-Binding ProteinMembrane GlycoproteinsAcute-Phase ProteinsCarrier ProteinsCulture Media, Serum-FreeInterleukin-6Lipopolysaccharide-Binding ProteinLipopolysaccharidesMembrane GlycoproteinsPyrogens

Identifiers

PMID39775542
PMCPMC11684592

What OpenQuestion 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 OpenQuestion graph.