Evidence map›Paper›PMID 24404168›Full record

ArticlePloS one2014

T cells detect intracellular DNA but fail to induce type I IFN responses: implications for restriction of HIV replication.

Randi K Berg, Stine H Rahbek, Emil Kofod-Olsen, Christian K Holm, Jesper Melchjorsen, David G Jensen, Anne Louise Hansen, Louise B Jørgensen, Lars Ostergaard, Martin Tolstrup and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. IFIH1 (MDA5) is required for innate immune detection of intron-containing RNA expressed from the HIV-1 provirus.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Transcriptomic analysis of the innate immune response toMolecular therapy. Nucleic acids · 2023
    Article
  9. Article
  10. Review
  11. Absence of cGAS-mediated type I IFN responses in HIV-1-infected T cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Article
  13. Article
  14. Review
  15. Rationale for stimulator of interferon genes-targeted cancer immunotherapy.European journal of cancer (Oxford, England : 1990) · 2017
    Review
  16. Review
  17. Review
  18. Review
  19. Advanced Design of Dumbbell-shaped Genetic Minimal Vectors Improves Non-coding and Coding RNA Expression.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    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

14 authors at 3 institutions in 1 country.

Randi K BergDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark.
Stine H RahbekDepartment of Biomedicine, Aarhus University, Aarhus, Denmark ; Aarhus Research Center for Innate Immunology, Aarhus, Denmark.
Emil Kofod-OlsenDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark ; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Christian K HolmDepartment of Biomedicine, Aarhus University, Aarhus, Denmark ; Aarhus Research Center for Innate Immunology, Aarhus, Denmark.
Jesper MelchjorsenDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark.
David G JensenDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark.
Anne Louise HansenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Louise B JørgensenDepartment of Virology, The State Serum Institute, Copenhagen, Denmark.
Lars OstergaardDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark.
Martin TolstrupDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark.
Carsten S LarsenDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark.
Søren R PaludanDepartment of Biomedicine, Aarhus University, Aarhus, Denmark ; Aarhus Research Center for Innate Immunology, Aarhus, Denmark.
Martin R JakobsenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark ; Aarhus Research Center for Innate Immunology, Aarhus, Denmark.
Trine H MogensenDepartment of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark ; Aarhus Research Center for Innate Immunology, Aarhus, Denmark.
Aarhus University Hospital · DKAarhus University · DKStatens Serum Institut · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIV infects key cell types of the immune system, most notably macrophages and CD4+ T cells. Whereas macrophages represent an important viral reservoir, activated CD4+ T cells are the most permissive cell types supporting high levels of viral replication. In recent years, it has been appreciated that the innate immune system plays an important role in controlling HIV replication, e.g. via interferon (IFN)-inducible restriction factors. Moreover, innate immune responses are involved in driving chronic immune activation and the pathogenesis of progressive immunodeficiency. Several pattern recognition receptors detecting HIV have been reported, including Toll-like receptor 7 and Retinoic-inducible gene-I, which detects viral RNA. Here we report that human primary T cells fail to induce strong IFN responses, despite the fact that this cell type does express key molecules involved in DNA signaling pathways. We demonstrate that the DNA sensor IFI16 migrates to sites of foreign DNA localization in the cytoplasm and recruits the signaling molecules stimulator of IFN genes and Tank-binding kinase, but this does not result in expression of IFN and IFN-stimulated genes. Importantly, we show that cytosolic DNA fails to affect HIV replication. However, exogenous treatment of activated T cells with type I IFN has the capacity to induce expression of IFN-stimulated genes and suppress HIV replication. Our data suggest the existence of an impaired DNA signaling machinery in T cells, which may prevent this cell type from activating cell-autonomous anti-HIV responses. This phenomenon could contribute to the high permissiveness of CD4+ T cells for HIV-1.

Indexed as

ApoptosisBiological TransportCD4-Positive T-LymphocytesCytokinesCytosolDNAHIV-1HIV InfectionsHumansInflammation MediatorsInterferon Type IInterleukin-2Leukocytes, MononuclearMembrane ProteinsProtein BindingProtein Serine-Threonine KinasesCytokinesDNAInflammation MediatorsInterferon Type IInterleukin-2Membrane ProteinsProtein Serine-Threonine KinasesSTING1 protein, humanSTING ProteinTBK1 protein, human

Identifiers

PMID24404168
PMCPMC3880311
OpenAlexW2012580035

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.