Evidence map›Paper›PMID 33585237›Full record

ArticleFrontiers in oncology2020

Lack of Viral Load Within Chronic Lymphoproliferative Disorder of Natural Killer Cells: What Is Outside the Leukemic Clone?

Edoardo Giussani, Andrea Binatti, Giulia Calabretto, Vanessa Rebecca Gasparini, Antonella Teramo, Cristina Vicenzetto, Gregorio Barilà, Monica Facco, Alessandro Coppe, Gianpietro Semenzato and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

12 authors at 2 institutions in 1 country.

Edoardo GiussaniDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Andrea BinattiDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Giulia CalabrettoDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Vanessa Rebecca GaspariniDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Antonella TeramoDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Cristina VicenzettoDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Gregorio BarilàDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Monica FaccoDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Alessandro CoppeDepartment of Maternal and Child Health, University of Padova, Padova, Italy.
Gianpietro SemenzatoDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Stefania BortoluzziDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Renato ZambelloDepartment of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
University of Padua · ITVeneto Institute of Molecular Medicine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large granular lymphocyte leukemias (LGLL) are sustained by proliferating cytotoxic T cells or NK cells, as happens in Chronic Lymphoproliferative Disorder of Natural Killer cells (CLPD-NK), whose etiology is only partly understood. Different hypotheses have been proposed on the original events triggering NK cell hyperactivation and transformation, including a role of viral agents. In this perspective, we revise the lines of evidence that suggested a pathogenetic role in LGLL of the exposure to retroviruses and that identified Epstein Barr Virus (EBV) in other NK cell leukemias and lymphomas and focus on the contrasting data about the importance of viral agents in CLPD-NK. EBV was detected in aggressive NK leukemias but not in the indolent CLPD-NK, where seroreactivity against HTLV-1 retrovirus envelope BA21 protein antigens has been reported in patients, although lacking clear evidence of HTLV infection. We next present original results of whole exome sequencing data analysis that failed to identify viral sequences in CLPD-NK. We recently demonstrated that proliferating NK cells of patients harbor several somatic lesions likely contributing to sustain NK cell proliferation. Thus, we explore whether "neoantigens" similar to the BA21 antigen could be generated by aberrancies present in the leukemic clone. In light of the literature and new data, we evaluated the intriguing hypothesis that NK cell activation can be caused by retroviral agents located outside the hematopoietic compartment and on the possible mechanisms involved with the prospects of immunotherapy-based approaches to limit the growth of NK cells in CLPD-NK disease.

Indexed as

chronic lymphoproliferative disorder of natural killer (NK) cellshepatocyteskiller immunoglobulin-like receptorsnatural killer cellspneumocytesretroviral infection

Identifiers

PMID33585237
PMCPMC7873950
OpenAlexW3125897413

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.