Evidence map›Paper›PMID 24362551›Full record

ArticleHaematologica2014

HLA-G is a component of the chronic lymphocytic leukemia escape repertoire to generate immune suppression: impact of the HLA-G 14 base pair (rs66554220) polymorphism.

Roberta Rizzo, Valentina Audrito, Paola Vacca, Davide Rossi, Davide Brusa, Marina Stignani, Daria Bortolotti, Giovanni D'Arena, Marta Coscia, Luca Laurenti and 6 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Genetic polymorphism association ofAmerican journal of translational research · 2024
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  7. Review
  8. Article
  9. Review
  10. Article
  11. NK Cells in Chronic Lymphocytic Leukemia and Their Therapeutic Implications.International journal of molecular sciences · 2021
    Review
  12. Article
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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

16 authors at 10 institutions in 2 countries.

Roberta Rizzosilvia.deaglio@unito.it or roberta.rizzo@unife.it.
Valentina Audrito
Paola Vacca
Davide Rossi
Davide Brusa
Marina Stignani
Daria Bortolotti
Giovanni D'Arena
Marta Coscia
Luca Laurenti
Francesco Forconi
Gianluca Gaidano
Maria Cristina Mingari
Lorenzo Moretta
Fabio Malavasi
Silvia Deaglio
University of Ferrara · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITItalian institute for Genomic Medicine · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversity of Genoa · ITCentro di Riferimento Oncologico della Basilicata · ITIstituto Giannina Gaslini · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Southampton · GBUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This work investigates the possibility that HLA-G, a molecule modulating innate and adaptive immunity, is part of an immune escape strategy of chronic lymphocytic leukemia cells. A 14 base pair insertion/deletion polymorphism (rs66554220) in the 3'-untranslated region of HLA-G influences mRNA stability and protein expression. The analysis of a cohort of patients with chronic lymphocytic leukemia confirmed that del/del individuals are characterized by higher levels of surface and soluble HLA-G than subjects with the other two genotypes. In line with its role in immunomodulation, the percentage of regulatory T lymphocytes is higher in del/del patients than in patients with the other genotypes and correlates with the amounts of surface or soluble HLA-G. Furthermore, addition of sHLA-G-rich plasma from patients with chronic lymphocytic leukemia induces natural killer cell apoptosis and impairs natural killer cell lysis, with effects proportional to the amount of soluble HLA-G added. Lastly, the presence of an HLA-G 14 base pair polymorphism is of prognostic value, with del/del patients showing reduced overall survival, as compared to those with other genotypes. These results suggest that: (i) the HLA-G 14 base pair polymorphism influences the levels of surface and soluble HLA-G expression, and (ii) the over-expression of HLA-G molecules contributes to creating tolerogenic conditions.

Indexed as

Polymorphism, GeneticFemaleGene ExpressionHLA-G AntigensHumansImmunophenotypingKiller Cells, NaturalLeukemia, Lymphocytic, Chronic, B-CellLymphocyte CountMalePrognosisRNA, MessengerTumor EscapeHLA-G AntigensRNA, Messenger

Identifiers

PMID24362551
PMCPMC4008099
OpenAlexW1796843950

What OpenQuestion holds

Textmetadata
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.