Evidence map›Paper›PMID 35775392›Full record

ArticleEuropean journal of haematology2022

Bone marrow CD3

Stefania Leone, Valentina Rubino, Anna Teresa Palatucci, Angela Giovazzino, Flavia Carriero, Giuseppe Cerciello, Fabrizio Pane, Giuseppina Ruggiero, Giuseppe Terrazzano

Open access · hybridAbstract read
In one paragraph

Article in European journal of haematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. TInternational journal of molecular sciences · 2024
    Article
  5. Immune Profile in COVID-19: Unveiling TInternational journal of molecular sciences · 2024
    Article
  6. Article
  7. Regulatory TCells · 2023
    Review
  8. Article
  9. Bone marrow CD3European journal of haematology · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Stefania LeoneDivisione di Ematologia, Dipartimento di Medicina Clinica e Chirurgia, Università di Napoli "Federico II", Naples, Italy.
Valentina RubinoDipartimento di Scienze Mediche Traslazionali, Università di Napoli "Federico II", Naples, Italy.
Anna Teresa PalatucciDipartimento di Scienze, Università della Basilicata, Potenza, Italy.
Angela GiovazzinoDipartimento di Scienze Mediche Traslazionali, Università di Napoli "Federico II", Naples, Italy.
Flavia CarrieroPh.D course in Science, Università della Basilicata, Potenza, 85100, Italy.
Giuseppe CercielloDivisione di Ematologia, Dipartimento di Medicina Clinica e Chirurgia, Università di Napoli "Federico II", Naples, Italy.
Fabrizio PaneDivisione di Ematologia, Dipartimento di Medicina Clinica e Chirurgia, Università di Napoli "Federico II", Naples, Italy.
Giuseppina RuggieroDipartimento di Scienze Mediche Traslazionali, Università di Napoli "Federico II", Naples, Italy.ORCID https://orcid.org/0000-0002-8975-6001
Giuseppe TerrazzanoDipartimento di Scienze Mediche Traslazionali, Università di Napoli "Federico II", Naples, Italy.
University of Naples Federico II · ITUniversity of Basilicata · IT

Funding

FISM-Fondazione Italiana Sclerosi Multipla - 2017/R/23 and financed or co-financed with the '5 per mille' public funding to Dr G. RuggieroProgramma Operativo Nazionale "Ricerca e Innovazione" 2014-2020 (PON "R&I" 2014-2020), for the project "Prodotti innovativi ad alto contenuto biotecnologico- INBIOMED" (Ministero Italiano dell'Università e della Ricerca, code ARS01_01081) to Dr G. Terrazzano
6 · The paper itself

Abstract

backgroundEmergence of dysplastic haematopoietic precursor/s, cytopenia and variable leukaemia risk characterise myelodysplastic syndromes (MDS). Impaired immune-regulation, preferentially affecting cytotoxic T cells (CTL), has been largely observed in MDS. Recently, we described the T

objectivesTo analyse the relationship between T

methodsPeripheral blood and BM specimens, obtained at disease onset in a cohort of 58 subjects, were analysed by immune-fluorescence and flow cytometry, to preserve the complexity of the biological sample.

resultsWe observed that a trend-increase of BM T

conclusionsThese data add T

Indexed as

Bone MarrowMyelodysplastic SyndromesBone Marrow CellsHumansT-Lymphocytes, CytotoxicT-Lymphocytes, RegulatoryT-Lymphocyte Subsetsbone marrowcytotoxic T-lymphocytesmyelodysplastic syndromeT lymphocytes regulatory

Identifiers

PMID35775392
PMCPMC9543123
OpenAlexW4283750426

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.