Evidence map›Paper›PMID 34467632›Full record

ArticleEMBO reports2021

Inhibition of IRGM establishes a robust antiviral immune state to restrict pathogenic viruses.

Parej Nath, Nishant Ranjan Chauhan, Kautilya Kumar Jena, Ankita Datey, Nilima Dinesh Kumar, Subhash Mehto, Saikat De, Tapas Kumar Nayak, Swatismita Priyadarsini, Kshitish Rout and 8 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Irgm1 Restrains CD8European journal of immunology · 2026
    Article
  3. Review
  4. Macrophages From Latently Infected Mice Have Trained Immunity to HSV-1.Investigative ophthalmology & visual science · 2026
    Article
  5. Autophagy and Bacterial infections.Autophagy reports · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Type I IFN signaling in the absence of IRGM1 promotesbioRxiv : the preprint server for biology · 2023
    Article
  11. Article
  12. Role of cGAS-Sting Signaling in Alzheimer's Disease.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Immunity-related GTPase IRGM at the intersection of autophagy, inflammation, and tumorigenesis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Frontiers in oncology · 2022
    Article
  19. Article
  20. 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

18 authors at 4 institutions in 2 countries.

Parej Nath *Cell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Nishant Ranjan Chauhan *Cell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.ORCID 0000-0002-9137-6024
Kautilya Kumar Jena *Cell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Ankita DateyMolecular Virology Lab, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Nilima Dinesh KumarDepartment of Biomedical Sciences of Cells and Systems, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0003-2788-0303
Subhash MehtoCell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Saikat DeMolecular Virology Lab, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Tapas Kumar NayakMolecular Virology Lab, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Swatismita PriyadarsiniCell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Kshitish RoutCell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Ramyasingh BalCell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Krushna C MurmuEpigenetic and Chromatin Biology Unit, Institute of Life Sciences, Bhubaneswar, India.ORCID 0000-0002-5568-680X
Manjula KaliaVirology Lab, Regional Centre for Biotechnology, NCR Biotech Science Cluster, Faridabad, India.ORCID 0000-0002-3376-3659
Srinivas PatnaikSchool of Biotechnology, KIIT University, Bhubaneswar, India.
Punit PrasadEpigenetic and Chromatin Biology Unit, Institute of Life Sciences, Bhubaneswar, India.
Fulvio ReggioriDepartment of Biomedical Sciences of Cells and Systems, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0003-2652-2686
Soma ChattopadhyayMolecular Virology Lab, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Santosh ChauhanCell Biology and Infectious Diseases Unit, Department of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.ORCID 0000-0001-9167-5107
Institute of Life Sciences · INUniversity Medical Center Groningen · NLKIIT University · INRegional Centre for Biotechnology · IN

Funding

Department of Biotechnology, Ministry of Science and Technology, India (DBT) BT/PR23942/BRB/10/1808/2019Department of Science and Technology, Ministry of Science and Technology, India (DST) DST/INSPIRE/04/2019/001857Department of Science and Technology, Ministry of Science and Technology, India (DST) EMR/2016/000854DST | Science and Engineering Research Board (SERB) CRG/2020/003480ENW KLEIN-1 OCENW.KLEIN.118Marie Sklodowska-Curie Cofund 713660Marie Sklodowska-Curie ETN 765912The Wellcome Trust DBT India Alliance (India Alliance) IA/I/15/2/502071Wellcome TrustZonMW TOP 91217002
6 · The paper itself

Abstract

The type I interferon (IFN) response is the major host arsenal against invading viruses. IRGM is a negative regulator of IFN responses under basal conditions. However, the role of human IRGM during viral infection has remained unclear. In this study, we show that IRGM expression is increased upon viral infection. IFN responses induced by viral PAMPs are negatively regulated by IRGM. Conversely, IRGM depletion results in a robust induction of key viral restriction factors including IFITMs, APOBECs, SAMHD1, tetherin, viperin, and HERC5/6. Additionally, antiviral processes such as MHC-I antigen presentation and stress granule signaling are enhanced in IRGM-deficient cells, indicating a robust cell-intrinsic antiviral immune state. Consistently, IRGM-depleted cells are resistant to the infection with seven viruses from five different families, including Togaviridae, Herpesviridae, Flaviviverdae, Rhabdoviridae, and Coronaviridae. Moreover, we show that Irgm1 knockout mice are highly resistant to chikungunya virus (CHIKV) infection. Altogether, our work highlights IRGM as a broad therapeutic target to promote defense against a large number of human viruses, including SARS-CoV-2, CHIKV, and Zika virus.

Indexed as

AnimalsAntiviral AgentsGTP-Binding ProteinsHumansMiceVirus DiseasesVirus ReplicationAntiviral AgentsGTP-Binding ProteinsIRGM protein, humanCHIKVIRGMIRGM1SARS-CoV-2ZIKV

Identifiers

PMID34467632
PMCPMC8567234
OpenAlexW3197718606

What Socratic 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 Socratic graph.