Evidence map›Paper›PMID 26229115›Full record

ArticleScience (New York, N.Y.)2015

Transmission of innate immune signaling by packaging of cGAMP in viral particles.

Matteo Gentili, Joanna Kowal, Mercedes Tkach, Takeshi Satoh, Xavier Lahaye, Cécile Conrad, Marilyn Boyron, Bérangère Lombard, Sylvère Durand, Guido Kroemer and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Science (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 187 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed, 2 pooled it
11.1field-weighted citation impact, top 1% 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

187 citing papers in PubMed, 2 syntheses or guidelines pooled it, 303 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  9. Article
  10. Extracellular cGAMP in health and disease.Molecular biomedicine · 2026
    Review
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  13. Article
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  15. Article
  16. Restoration of cGAS in cancer cells promotes antitumor immunity via transfer of cancer cell-generated cGAMP.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Review
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  19. A diverse family of bacterial deubiquitinases is defined by theProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Article

127 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

Matteo GentiliINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France.
Joanna KowalINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France.
Mercedes TkachINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France.
Takeshi SatohINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France.
Xavier LahayeINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France.
Cécile ConradINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France.
Marilyn BoyronCentre d'Immunologie de Marseille-Luminy, Aix Marseille Université UM2, INSERM U1104, CNRS UMR7280, 13288 Marseille, France.
Bérangère LombardLaboratoire de Spectrométrie de Masse Protéomique, Institut Curie, Paris, France.
Sylvère DurandLabex Dendritic Cell Biology (DCBIOL), Paris, France.
Guido KroemerMetabolomics and Cell Biology Platforms, Gustave Roussy Comprehensive Cancer Institute, 94805 Villejuif, France.
Damarys LoewLaboratoire de Spectrométrie de Masse Protéomique, Institut Curie, Paris, France.
Marc DalodCentre d'Immunologie de Marseille-Luminy, Aix Marseille Université UM2, INSERM U1104, CNRS UMR7280, 13288 Marseille, France.
Clotilde ThéryINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France. Labex Dendritic Cell Biology (DCBIOL), Paris, France.
Nicolas ManelINSERM U932, Immunity and Cancer Unit, Institut Curie, Paris, France. Labex Dendritic Cell Biology (DCBIOL), Paris, France. Labex Vaccine Research Institute (VRI), Paris, France. nicolas.manel@curie.fr.
Institut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infected cells detect viruses through a variety of receptors that initiate cell-intrinsic innate defense responses. Cyclic guanosine monophosphate (GMP)-adenosine monophosphate (AMP) synthase (cGAS) is a cytosolic sensor for many DNA viruses and HIV-1. In response to cytosolic viral DNA, cGAS synthesizes the second messenger 2'3'-cyclic GMP-AMP (cGAMP), which activates antiviral signaling pathways. We show that in cells producing virus, cGAS-synthesized cGAMP can be packaged in viral particles and extracellular vesicles. Viral particles efficiently delivered cGAMP to target cells. cGAMP transfer by viral particles to dendritic cells activated innate immunity and antiviral defenses. Finally, we show that cell-free murine cytomegalovirus and Modified Vaccinia Ankara virus contained cGAMP. Thus, transfer of cGAMP by viruses may represent a defense mechanism to propagate immune responses to uninfected target cells.

Indexed as

Second Messenger SystemsAnimalsChlorocebus aethiopsCytosolDendritic CellsGenetic VectorsHeLa CellsHerpesviridae InfectionsHIV-1HIV InfectionsHumansImmunity, InnateMiceMice, Inbred C57BLMuromegalovirusNucleotides, Cycliccyclic guanosine monophosphate-adenosine monophosphateNucleotides, Cyclic

Identifiers

PMID26229115
OpenAlexW1933048492

What OpenQuestion holds

Textmetadata
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.