Evidence map›Paper›PMID 33459589›Full record

ArticleeLife2021

Cytomegalovirus restricts ICOSL expression on antigen-presenting cells disabling T cell co-stimulation and contributing to immune evasion.

Guillem Angulo, Jelena Zeleznjak, Pablo Martínez-Vicente, Joan Puñet-Ortiz, Hartmut Hengel, Martin Messerle, Annette Oxenius, Stipan Jonjic, Astrid Krmpotić, Pablo Engel and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. A viral glycoprotein targets IgGEMBO molecular medicine · 2026
    Article
  2. Article
  3. Article
  4. Immune surveillance of cytomegalovirus in tissues.Cellular & molecular immunology · 2024
    Review
  5. Article
  6. Article
  7. 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

11 authors at 6 institutions in 4 countries.

Guillem Angulo *Immunology Unit, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.ORCID 0000-0001-7086-9754
Jelena Zeleznjak *Center for Proteomics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.ORCID 0000-0001-6619-3675
Pablo Martínez-VicenteImmunology Unit, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.ORCID 0000-0001-9277-1950
Joan Puñet-OrtizImmunology Unit, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.
Hartmut HengelInstitute of Virology, University Medical Center, Albert-Ludwigs-University Freiburg, Freiburg, Germany.ORCID 0000-0002-3482-816X
Martin MesserleInstitute of Virology, Hannover Medical School, Hannover, Germany.
Annette OxeniusInstitute of Microbiology, Department of Biology, ETH Zürich, Zürich, Switzerland.
Stipan JonjicCenter for Proteomics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Astrid KrmpotićDepartment of Histology and Embryology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Pablo EngelImmunology Unit, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.ORCID 0000-0001-8410-252X
Ana AnguloImmunology Unit, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-5792-1164
Consorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESUniversity of Rijeka · HRETH Zurich · CHMedizinische Hochschule Hannover · DEUniversitat de Barcelona · ESUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viral infections are controlled, and very often cleared, by activated T lymphocytes. The inducible co-stimulator (ICOS) mediates its functions by binding to its ligand ICOSL, enhancing T-cell activation and optimal germinal center (GC) formation. Here, we show that ICOSL is heavily downmodulated during infection of antigen-presenting cells by different herpesviruses. We found that, in murine cytomegalovirus (MCMV), the immunoevasin m138/fcr-1 physically interacts with ICOSL, impeding its maturation and promoting its lysosomal degradation. This viral protein counteracts T-cell responses, in an ICOS-dependent manner, and limits virus control during the acute MCMV infection. Additionally, we report that blockade of ICOSL in MCMV-infected mice critically regulates the production of MCMV-specific antibodies due to a reduction of T follicular helper and GC B cells. Altogether, these findings reveal a novel mechanism evolved by MCMV to counteract adaptive immune surveillance, and demonstrates a role of the ICOS:ICOSL axis in the host defense against herpesviruses.

Indexed as

Immune EvasionAnimalsHerpesviridae InfectionsInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator ProteinMiceMuromegalovirusT-LymphocytesInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator Proteinantigen presenting cellscd275cytomegalovirusherpesvirusicoslimmunologyinflammationmouset-cell co-stimulationviral immune evasionvirus

Identifiers

PMID33459589
PMCPMC7840182
OpenAlexW3125939843

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.