Evidence map›Paper›PMID 42430241›Full record

ArticleSTAR protocols2026

Protocol for profiling circulating T cell subsets, their homing and regulatory markers, in pediatric samples using a 4-laser BD LSRII.

Tomas Thon, Jan Svoboda, Zaneta Slavickova, Eliska Kopelentova, Dagmar Srutkova, Stepan Coufal, Zuzana Reiss, Miloslav Kverka, Stepanka Capkova, Jana Cadova and 4 more

Abstract read
In one paragraph

Article in STAR protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Tomas ThonLaboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic.
Jan SvobodaCytometry and Microscopy Core Facility, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic. Electronic address: svoboda@biomed.cas.cz.
Zaneta SlavickovaLaboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic.
Eliska KopelentovaDepartment of Immunology, 2nd Faculty of Medicine, Charles University and Motol and Homolka University Hospital, Prague, Czech Republic.
Dagmar SrutkovaLaboratory of Gnotobiology, Institute of Microbiology of the Czech Academy of Sciences, Novy Hradek, Czech Republic.
Stepan CoufalLaboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic.
Zuzana ReissLaboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic.
Miloslav KverkaLaboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic.
Stepanka CapkovaDepartment of Paediatric Dermatology, Motol and Homolka University Hospital, Prague, Czech Republic.
Jana CadovaDepartment of Paediatric Dermatology, Motol and Homolka University Hospital, Prague, Czech Republic.
Anna SedivaDepartment of Immunology, 2nd Faculty of Medicine, Charles University and Motol and Homolka University Hospital, Prague, Czech Republic.
Helena Tlaskalova-HogenovaLaboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic; Institute of Clinical Immunology and Allergology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Andrea PolouckovaDepartment of Immunology, 2nd Faculty of Medicine, Charles University and Motol and Homolka University Hospital, Prague, Czech Republic.
Zuzana Jiraskova ZakostelskaLaboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czech Republic. Electronic address: zakostelska@biomed.cas.cz.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we present a protocol for profiling T cell subsets, regulatory phenotypes, and gut- and skin-homing markers of unstimulated cells or those stimulated with staphylococcal enterotoxin B (SEB), lipopolysaccharide (LPS), or zymosan (ZYM). We describe steps for isolation, cryopreservation, thawing, stimulation, and multiparameter flow cytometric analysis of human peripheral blood mononuclear cells (PBMCs). Use of the multicolored panel detailed in this protocol allows full utilization of the valuable samples with the minimal possible volume of collected pediatric blood. For complete details on the use and execution of this protocol, please refer to Thon et al.

Indexed as

Cell isolationFlow CytometryImmunology

Identifiers

PMID42430241
PMCPMC13380796

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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.