Evidence map›Paper›PMID 34110660›Full record

ArticleHepatology (Baltimore, Md.)2021

Immune Activation Induces Telomeric DNA Damage and Promotes Short-Lived Effector T Cell Differentiation in Chronic HCV Infection.

Lam Nhat Nguyen, Lam Ngoc Thao Nguyen, Juan Zhao, Madison Schank, Xindi Dang, Dechao Cao, Sushant Khanal, Bal Krishna Chand Thakuri, Jinyu Zhang, Zeyuan Lu and 6 more

Open access · greenAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. 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

16 authors at 1 institution in 1 country.

Lam Nhat NguyenCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Lam Ngoc Thao NguyenCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Juan ZhaoCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Madison SchankCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Xindi DangCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Dechao CaoCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Sushant KhanalCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Bal Krishna Chand ThakuriCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Jinyu ZhangCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Zeyuan LuCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Xiao Y WuCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Mohamed El GazzarCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Shunbin NingCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Ling WangCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Jonathan P MoormanCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.
Zhi Q YaoCenter of Excellence in Inflammation, Infectious Disease and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN.ORCID 0000-0002-1848-1071
East Tennessee State University · US

Funding

miRNA-mediated premature T cell aging in vaccine failure during viral infectionR01AI114748 · NIAID · EAST TENNESSEE STATE UNIVERSITY · PI YAO, ZHI Q. · 2015 to 2019
$1.9M
Multiuser Advanced Biosafe Flow CytometerS10OD021572 · OD · EAST TENNESSEE STATE UNIVERSITY · PI MOORMAN, JONATHAN P · 2017 to 2017
$553k
Telomere loss and T cell aging in HBV vaccine response in HIV-infected individualR21AI138598 · NIAID · EAST TENNESSEE STATE UNIVERSITY · PI YAO, ZHI Q. · 2018 to 2019
$407k
Multiuser Advanced Confocal MicroscopeIS1BX004778 · VA · JAMES H QUILLEN VA MEDICAL CENTER · PI YAO, ZHI Q. · 2019 to 2019
–
Telomere attrition and T cell aging in vaccine failure during HIV infectionI01BX002670 · VA · JAMES H QUILLEN VA MEDICAL CENTER · PI YAO, ZHI Q. · 2016 to 2025
–
Droplet Digital PCR SystemIS1BX005519 · VA · JAMES H QUILLEN VA MEDICAL CENTER · PI YAO, ZHI Q. · 2021 to 2021
–
Telomere loss and T cell aging in HBV vaccine response in HCV-infected individualI01BX004281 · VA · JAMES H QUILLEN VA MEDICAL CENTER · PI YAO, ZHI Q. · 2019 to 2022
–
ShEEP Proposal for a Multiuser Advanced Biosafe Flow CytometerIS1BX003540 · VA · JAMES H QUILLEN VA MEDICAL CENTER · PI YAO, ZHI Q. · 2016 to 2016
–
BLRD VA I01 BX002670BLRD VA I01 BX004281BLRD VA IS1 BX003540BLRD VA IS1 BX004778BLRD VA IS1 BX005519NIAID NIH HHS R01 AI114748NIAID NIH HHS R21 AI138598NIH HHS S10 OD021572
6 · The paper itself

Abstract

BACKGROUND AND

aimsHepatitis C virus (HCV) leads to a high rate of chronic infection and T cell dysfunction. Although it is well known that chronic antigenic stimulation is a driving force for impaired T cell functions, the precise mechanisms underlying immune activation-induced T cell dysfunctions during HCV infection remain elusive. APPROACH AND

resultsHere, we demonstrated that circulating CD4

conclusionsThese results suggest that modulation of immune activation through inhibiting Akt signaling and protecting telomeres through enhancing TRF2 expression may open therapeutic strategies to fine tune the adaptive immune responses in the setting of persistent immune activation and inflammation during chronic HCV infection.

Indexed as

AdultAgedApoptosisCD4-Positive T-LymphocytesCell DifferentiationCells, CulturedDNA DamageFemaleGene Knockdown TechniquesHepacivirusHepatitis C, ChronicHumansLymphocyte ActivationMaleMiddle AgedPersistent InfectionMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, ViralTelomeric Repeat Binding Protein 2TERF2 protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID34110660
PMCPMC8542603
OpenAlexW3166731822

What OpenQuestion holds

Textmetadata
LicenceTDM
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.