Evidence map›Paper›PMID 25505292›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2015

Profiling T cell activation using single-molecule fluorescence in situ hybridization and flow cytometry.

Yuri Bushkin, Felix Radford, Richard Pine, Alfred Lardizabal, Bonita T Mangura, Maria Laura Gennaro, Sanjay Tyagi

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2015. 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
2.8field-weighted citation impact, top 10% 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, 30 citations in OpenAlex.

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  6. High-fidelity amplified FISH for the detection and allelic discrimination of single mRNA molecules.Proceedings of the National Academy of Sciences of the United States of America · 2019
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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

7 authors at 1 institution in 1 country.

Yuri BushkinPublic Health Research Institute, New Jersey Medical School, Rutgers University, Newark, NJ 07103; and.
Felix RadfordPublic Health Research Institute, New Jersey Medical School, Rutgers University, Newark, NJ 07103; and.
Richard PinePublic Health Research Institute, New Jersey Medical School, Rutgers University, Newark, NJ 07103; and.
Alfred LardizabalGlobal Tuberculosis Institute, New Jersey Medical School, Rutgers University, Newark, NJ 07103.
Bonita T ManguraGlobal Tuberculosis Institute, New Jersey Medical School, Rutgers University, Newark, NJ 07103.
Maria Laura GennaroPublic Health Research Institute, New Jersey Medical School, Rutgers University, Newark, NJ 07103; and.
Sanjay TyagiPublic Health Research Institute, New Jersey Medical School, Rutgers University, Newark, NJ 07103; and bushkiyu@njms.rutgers.edu sanjay.tyagi@rutgers.edu.ORCID http://orcid.org/0000-0001-7303-5827
Rutgers, The State University of New Jersey · US

Funding

FISH-Flow platform for host-based tuberculosis diagnosticsR01AI104615 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI GENNARO, MARIA LAURA · 2013 to 2017
$5.5M
Rapid Analysis of Single T Cell Immunity Signatures in TuberculosisR01AI106036 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI BUSHKIN, YURI, GENNARO, MARIA LAURA · 2012 to 2016
$3.8M
NIAID NIH HHS AI104615NIAID NIH HHS AI106036NIAID NIH HHS R01 AI104615NIAID NIH HHS R01 AI106036
6 · The paper itself

Abstract

Flow cytometric characterization of Ag-specific T cells typically relies on detection of protein analytes. Shifting the analysis to detection of RNA would provide several significant advantages, which we illustrate by developing a new host immunity-based platform for detection of infections. Cytokine mRNAs synthesized in response to ex vivo stimulation with pathogen-specific Ags are detected in T cells with single-molecule fluorescence in situ hybridization followed by flow cytometry. Background from pre-existing in vivo analytes is lower for RNAs than for proteins, allowing greater sensitivity for detection of low-frequency cells. Moreover, mRNA analysis reveals kinetic differences in cytokine expression that are not apparent at the protein level but provide novel insights into gene expression programs expected to define different T cell subsets. The utility of probing immunological memory of infections is demonstrated by detecting T cells that recognize mycobacterial and viral Ags in donors exposed to the respective pathogens.

Indexed as

Lymphocyte ActivationAdultAgedAntigens, BacterialCytokinesFemaleFlow CytometryHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedRNA, MessengerT-LymphocytesTuberculosis, PulmonaryAntigens, BacterialCytokinesRNA, Messenger

Identifiers

PMID25505292
PMCPMC4350577
OpenAlexW1928259156

What OpenQuestion holds

Textmetadata
LicenceTDM
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.