Evidence map›Paper›PMID 32153407›Full record

ArticleFrontiers in pharmacology2020

The P2X7 Receptor 489C>T Gain of Function Polymorphism Favors HHV-6A Infection and Associates With Female Idiopathic Infertility.

Anna Pegoraro, Daria Bortolotti, Roberto Marci, Elisabetta Caselli, Simonetta Falzoni, Elena De Marchi, Francesco Di Virgilio, Roberta Rizzo, Elena Adinolfi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. P2X7 Variants in Pathophysiology.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. P2RX7 at the Host-Pathogen Interface of Infectious Diseases.Microbiology and molecular biology reviews : MMBR · 2021
    Review
  11. Review
  12. Review
  13. The P2X7 purinergic receptor: a potential therapeutic target for lung cancer.Journal of cancer research and clinical oncology · 2020
    Review
  14. Article
  15. Article
  16. Review
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

9 authors at 2 institutions in 2 countries.

Anna PegoraroDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Daria BortolottiDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Roberto MarciDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Elisabetta CaselliDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Simonetta FalzoniDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Elena De MarchiDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Francesco Di VirgilioDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Roberta RizzoDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Elena AdinolfiDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
University of Ferrara · ITUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The P2X7 receptor (P2X7R) is an ATP-gated ion channel known for its proinflammatory activity. Despite its participation in host defense against pathogens, the role played in viral infections, notably those caused by herpes viruses, has been seldom studied. Here we investigated the effect of P2X7R expression on human herpes virus 6 A (HHV-6A) infection of P2X7R-expressing HEK293 cells. We show that functional P2X7R increases while its blockade decreases viral load. Interestingly, HHV-6A infection was enhanced in HEK293 cells transfected with P2X7R cDNA bearing the gain of function 489C>T SNP (rs208294, replacing a histidine for tyrosine at position 155). The P2X7R 489C>T polymorphism correlated with HHV-6A infection also in a cohort of 50 women affected with idiopathic infertility, a condition previously shown to correlate with HHV-6A infection. None of the infertile women infected by HHV-6A was homozygote for 489CC genotype, while on the contrary HHV-6A infection significantly associated with the presence of the rs208294 allele. Levels of soluble human leukocyte antigen G (sHLA-G), a factor promoting embryo implant, measured in uterine flushings negatively correlated with the 489TT genotype and HHV-6A infection, while proinflammatory cytokines interleukins 1α (IL-1α), 1β (IL-1β), and 8 (IL-8) positively correlated with both the 489T allele presence and viral infection. Taken together these data point to the P2X7R as a new therapeutic target to prevent HHV-6A infection and the associated infertility.

Indexed as

female infertilityHHV-6A infectionHLA-GP2X7P2X7 489C>T polymorphism

Identifiers

PMID32153407
PMCPMC7046806
OpenAlexW3008432224

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.