Evidence map›Paper›PMID 38115685›Full record

ArticleJournal of clinical laboratory analysis2023

High-throughput RNA sequencing of the T cell receptor alpha and beta chains for simultaneous clonality and biological analyses in Sezary syndrome.

Gonzalo Blanco, Daniel López-Aventín, Ramon M Pujol, Andrea Gómez-Llonín, Anna Puiggros, Manuela López-Sánchez, Teresa Estrach, Mª Pilar García-Muret, Ingrid López-Lerma, Octavio Servitje and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2023. 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
0.6field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  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

15 authors at 9 institutions in 2 countries.

Gonzalo BlancoGrup de Recerca Translacional en Neoplàsies Hematològiques, Cancer Research Programme, IMIM-Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0001-6557-3764
Daniel López-AventínServei de Dermatologia, Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0001-5097-5621
Ramon M PujolServei de Dermatologia, Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-5622-6055
Andrea Gómez-LlonínGrup de Recerca Translacional en Neoplàsies Hematològiques, Cancer Research Programme, IMIM-Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-7470-6730
Anna PuiggrosGrup de Recerca Translacional en Neoplàsies Hematològiques, Cancer Research Programme, IMIM-Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0001-9627-4978
Manuela López-SánchezServicio de Inmunología, Hospital Clínico Universitario Virgen de la Arrixaca-IMIB, Murcia, Spain.ORCID https://orcid.org/0000-0002-5094-0266
Teresa EstrachServei de Dermatologia, Hospital Clínic, IDIBAPS, Universitat de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0002-4601-2811
Mª Pilar García-MuretServei de Dermatologia, Hospital de Sant Pau, Barcelona, Spain.ORCID https://orcid.org/0000-0003-1714-5815
Ingrid López-LermaServei de Dermatologia, Hospital Vall d'Hebron, Barcelona, Spain.ORCID https://orcid.org/0000-0002-7690-8926
Octavio ServitjeServei de Dermatologia, Hospital de Bellvitge, Barcelona, Spain.ORCID https://orcid.org/0000-0002-9910-9617
Beatriz BellosilloGrup de Recerca Clínica Aplicada en Neoplàsies Hematològiques, Cancer Research Programme, IMIM-Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-5335-2726
Manuel MuroServicio de Inmunología, Hospital Clínico Universitario Virgen de la Arrixaca-IMIB, Murcia, Spain.ORCID https://orcid.org/0000-0001-9987-0994
Blanca EspinetGrup de Recerca Translacional en Neoplàsies Hematològiques, Cancer Research Programme, IMIM-Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-4294-8145
Raquel RabionetDepartament de Genètica, Microbiologia i Estadística, Universitat de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0001-5006-8140
Fernando GallardoGrup de Recerca Translacional en Neoplàsies Hematològiques, Cancer Research Programme, IMIM-Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-8996-3828
Hospital Del Mar · ESHospital Universitario Virgen de la Arrixaca · ESBellvitge University Hospital · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital de Sant Pau · ESHospital Sant Joan de Déu Barcelona · ESNorthwell Health · USUniversitat Autònoma de Barcelona · ESVall d'Hebron Hospital Universitari · ES

Funding

Generalitat de Catalunya 2017/SGR437Generalitat de Catalunya 2017/SGR738Generalitat de Catalunya 2021/SGR025Instituto de Salud Carlos III, Spanish Ministry of Economy and Competitiveness PI18/00021Instituto de Salud Carlos III, Spanish Ministry of Economy and Competitiveness PI21/00390
6 · The paper itself

Abstract

backgroundPrevious investigations pointed out a role for antigen stimulation in Sezary syndrome (SS). High-throughput sequencing of the T cell receptor (TR) offers several applications beyond diagnostic purposes, including the study of T cell pathogenesis.

methodsWe performed high-throughput RNA sequencing of the TR alpha (TRA) and beta (TRB) genes focusing on the complementarity-determining region 3 (CDR3) in 11 SS and one erythrodermic mycosis fungoides (MF) patients. Five psoriasis patients were employed as controls. Peripheral blood CD4

resultsHighly expanded predominant TRA and TRB CDR3 were only found in SS patients (median frequency: 94.4% and 93.7%). No remarkable CDR3 expansions were observed in psoriasis patients (median frequency of predominant TRA and TRB CDR3: 0.87% and 0.69%, p < 0.001 compared to SS). CDR3 almost identical to the predominant were identified within each SS patient and were exponentially correlated with frequencies of the predominant CDR3 (R

conclusionsBesides detecting clonality, these findings shed light on the nature of SS-related antigens, pointing to RNA sequencing as a useful tool for simultaneous clonality and biological analysis in SS.

Indexed as

PsoriasisSezary SyndromeSkin NeoplasmsComplementarity Determining RegionsHigh-Throughput Nucleotide SequencingHumansReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaComplementarity Determining RegionsReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaantigen restrictioncomplementarity determining regionmycosis fungoidesRNA sequencingSezary syndromeT cell receptor

Identifiers

PMID38115685
PMCPMC10756948
OpenAlexW4390012912

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.