ArticleMolecular biotechnology2003
Multiple color immunofluorescence for cytokine detection at the single-cell level.
Article in Molecular biotechnology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Flow cytometric detection of p38 MAPK phosphorylation and intracellular cytokine expression in peripheral blood subpopulations from patients with autoimmune rheumatic diseases.Journal of immunology research · 2014Article
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Detection of cytokines and identification of the producer cells are essential to define the interplay and the role of distinct leukocyte subsets in the development of immune and inflammatory responses. Several methods used to study cytokine expression are based on detection of the encoding mRNA (Northern blot, RNase protection assay, RT-PCR) or of protein in the supernatant from stimulated cells (ELISA, RIA, ELISPOT). These are simple and useful, but have limitations related to the need of using purified cell populations to precisely define the effector cells, and exception made for RT-PCR and ELISPOT assays, the requirement for relatively large numbers of cells for sufficient resolution. Here we present a method based on immunofluorescence (flow cytofluorimetry) to detect intracellular accumulation of cytokines in mixed leukocyte populations. It has the distinct advantage of: 1. identifying producing cells in mixed cell populations, 2. comparing quantitatively the levels of production within cells in a given population and among different cell subsets, and 3. defining simultaneous production of distinct cytokines by a single cell type. The detailed description/discussion of the method uses natural killer (NK) cells as an example, but this method can be applied to the study of other cell types, and is of special interest/use when analyzing subsets present in very low proportion.
Indexed as
Identifiers
12665694What OpenQuestion holds
Registered trials
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.