Evidence map›Paper›PMID 32850472›Full record

ArticleFrontiers in cellular and infection microbiology2020

Per2 Upregulation in Circulating Hematopoietic Progenitor Cells During Chronic HIV Infection.

Veronica Bordoni, Eleonora Tartaglia, Giulia Refolo, Alessandra Sacchi, Germana Grassi, Andrea Antinori, Gian Maria Fimia, Chiara Agrati

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Resveratrol againstTropical medicine and infectious disease · 2023
    Article
  3. Review
  4. Review
  5. 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

8 authors at 1 institution in 1 country.

Veronica BordoniLaboratory of Cellular Immunology, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Eleonora TartagliaLaboratory of Cellular Immunology, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Giulia RefoloLaboratory of Cell Biology and Electron Microscopy, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Alessandra SacchiLaboratory of Cellular Immunology, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Germana GrassiLaboratory of Cellular Immunology, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Andrea AntinoriClinical Department, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Gian Maria FimiaLaboratory of Cell Biology and Electron Microscopy, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Chiara AgratiLaboratory of Cellular Immunology, National Institute for Infectious Diseases "L. Spallanzani" IRCCS, Rome, Italy.
Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic HIV infection accelerates immune aging and is associated with abnormal hemato-lymphopoiesis, but the relationship between HIV-induced aging and Hematopoietic Progenitor Cells (HPC) function is not well-defined. In the context of aging, it has been demonstrated using a murine model that Per2 (Period circadian clock 2) is a negative regulator of HPC survival and lineage potential. A possible involvement of Per2 modulation on hematopoietic failure during HIV infection has not yet been investigated. The aim of this study was to analyze whether Per2 is differently expressed and regulated on HPC during HIV infection, possibly providing a therapeutic target to restore lymphoid potential in the HPC compartment. To this purpose, Per2 expression in circulating HPC was compared in 69 chronic HIV infected patients under successful ART and in matched 30 uninfected healthy donors (HD). HPC aging was assessed by measuring relative telomere length (RTL), and HPC functionality was evaluated by Colony Forming Cell (CFC) assay from both

Indexed as

HIV InfectionsAgedAgingAnimalsCell DifferentiationHematopoietic Stem CellsHumansMicePeriod Circadian ProteinsUp-RegulationPER2 protein, humanPer2 protein, mousePeriod Circadian Proteinshematopoietic progenitor cellsHIVperiod circadian clock 2senescenceSirtuin 1telomere length

Identifiers

PMID32850472
PMCPMC7396677
OpenAlexW3045010060

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.