Evidence map›Paper›PMID 30153311›Full record

ArticlePLoS pathogens2018

Control of primary mouse cytomegalovirus infection in lung nodular inflammatory foci by cooperation of interferon-gamma expressing CD4 and CD8 T cells.

Yvonne Lueder, Katrin Heller, Christiane Ritter, Kirsten A Keyser, Karen Wagner, Xiaokun Liu, Martin Messerle, Felix R Stahl, Stephan Halle, Reinhold Förster

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2018. 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
1.5field-weighted citation impact, top 18% 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, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Immune surveillance of cytomegalovirus in tissues.Cellular & molecular immunology · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. CD4Journal of virology · 2022
    Article
  12. Article
  13. The CD8Microbiology and molecular biology reviews : MMBR · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Cytomegalovirus (CMV) Pneumonitis: Cell Tropism, Inflammation, and Immunity.International journal of molecular sciences · 2019
    Review
  18. Article
  19. Review
  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

10 authors at 1 institution in 1 country.

Yvonne LuederInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Katrin HellerInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Christiane RitterInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Kirsten A KeyserInstitute of Virology, Hannover Medical School, Hannover, Germany.
Karen WagnerInstitute of Virology, Hannover Medical School, Hannover, Germany.
Xiaokun LiuInstitute of Immunology, Hannover Medical School, Hannover, Germany.ORCID 0000-0003-0732-7404
Martin MesserleInstitute of Virology, Hannover Medical School, Hannover, Germany.
Felix R StahlInstitute of Immunology, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-7443-8967
Stephan HalleInstitute of Immunology, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-7624-7005
Reinhold FörsterInstitute of Immunology, Hannover Medical School, Hannover, Germany.ORCID 0000-0001-6190-7923
Medizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (CMV) and mouse cytomegalovirus (MCMV) infection share many characteristics. Therefore infection of mice with MCMV is an important tool to understand immune responses and to design vaccines and therapies for patients at the risk of severe CMV disease. In this study, we investigated the immune response in the lungs following acute infection with MCMV. We used multi-color fluorescence microscopy to visualize single infected and immune cells in nodular inflammatory foci (NIFs) that formed around infected cells in the lungs. These NIFs consisted mainly of myeloid cells, T cells, and some NK cells. We found that the formation of NIFs was essential to reduce the number of infected cells in the lung tissue, showing that NIFs were sites of infection as well as sites of immune response. Comparing mice deficient for several leukocyte subsets, we identified T cells to be of prime importance for restricting MCMV infection in the lung. Moreover, T cells had to be present in NIFs in high numbers, and CD4 as well as CD8 T cells supported each other to efficiently control virus spread. Additionally, we investigated the effects of perforin and interferon-gamma (IFNγ) on the virus infection and found important roles for both mechanisms. NK cells and T cells were the major source for IFNγ in the lung and in in vitro assays we found that IFNγ had the potential to reduce plaque growth on primary lung stromal cells. Notably, the T cell-mediated control was shown to be perforin-independent but IFNγ-dependent. In total, this study systematically identifies crucial antiviral factors present in lung NIFs for early containment of a local MCMV infection at the single cell level.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDNA-Binding ProteinsHerpesviridae InfectionsImmunity, CellularInterferon-gammaLungMiceMice, Inbred C57BLMice, KnockoutMuromegalovirusPneumoniaDNA-Binding ProteinsInterferon-gammaRag2 protein, mouse

Identifiers

PMID30153311
PMCPMC6112668
OpenAlexW2889451681

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.