Evidence map›Paper›PMID 31440240›Full record

ArticleFrontiers in immunology2019

Maintenance of Functional CD57+ Cytolytic CD4+ T Cells in HIV+ Elite Controllers.

Chansavath Phetsouphanh, Daniel Aldridge, Emanuele Marchi, C Mee Ling Munier, Jodi Meyerowitz, Lyle Murray, Cloete Van Vuuren, Dominique Goedhals, Sarah Fidler, Anthony Kelleher and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Cytotoxic CD4Frontiers in immunology · 2023
    Review
  12. Article
  13. Uncovering the significance of expanded CD8Frontiers in immunology · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Functional Characteristics and Phenotypic Plasticity of CD57Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  20. 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

12 authors at 5 institutions in 3 countries.

Chansavath PhetsouphanhPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Daniel AldridgePeter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Emanuele MarchiPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
C Mee Ling MunierDepartment of Medicine, University of New South Wales, Sydney, NSW, Australia.
Jodi MeyerowitzPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Lyle MurrayPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Cloete Van VuurenMilitary Hospital, Bloemfontein, South Africa.
Dominique GoedhalsNational Health Laboratory Service, Division of Virology, University of the Free State, Bloemfontein, South Africa.
Sarah FidlerImperial College London, London, United Kingdom.
Anthony KelleherDepartment of Medicine, University of New South Wales, Sydney, NSW, Australia.
Paul KlenermanPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
John FraterPeter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Medawar Building for Pathogen Research · GBUniversity of Oxford · GBUNSW Sydney · AUImperial College London · GBUniversity of the Free State · ZA

Funding

Medical Research Council MR/L00528X/1Medical Research Council MR/L006588/1Medical Research Council MR/P011233/1Wellcome Trust 109965/Z/15/Z
6 · The paper itself

Abstract

Cytolytic CD4+ T cells play a prominent role in chronic viral infection. CD4+ CTLs clones specific for HIV-1 Nef and Gag are capable of killing HIV-1 infected CD4+ T cells and macrophages. Additionally, HIV-specific cytolytic CD4+ T cell responses in acute HIV infection are predictive of disease progression. CD57 expression on CD4s identifies cytolytic cells. These cells were dramatically increased in chronic HIV infection. CD57 expression correlated with cytolytic granules, granzyme B and perforin expression. They express lower CCR5 compared to CD57- cells, have less HIV total DNA, and were a minor component of the HIV reservoir. A small percentage of CD57+ CD4+ CTLs from EC were HIV-specific, could upregulate IFNγ with Gag peptide stimulation, express cytolytic granule markers and maintain Tbet

Indexed as

HIV Long-Term SurvivorsBiomarkersCD4-Positive T-LymphocytesCD57 AntigensCytokinesCytotoxicity, ImmunologicDisease ProgressionHIV InfectionsHumansImmunologic MemoryImmunophenotypingLymphocyte ActivationSuperantigensT-Lymphocyte SubsetsTranscriptomeViral LoadBiomarkersCD57 AntigensCytokinesSuperantigensCD4 T cellscytotoxic T cellsHIVT cellsviral immunology

Identifiers

PMID31440240
PMCPMC6694780
OpenAlexW2963209862

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.