Evidence map›Paper›PMID 36016196›Full record

ArticleVaccines2022

Identification and Characterization of Epithelial Cell-Derived Dense Bodies Produced upon Cytomegalovirus Infection.

Estéfani García-Ríos, María Josefa Rodríguez, María Carmen Terrón, Daniel Luque, Pilar Pérez-Romero

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. 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

5 authors at 1 institution in 1 country.

Estéfani García-RíosNational Center for Microbiology, Instituto de Salud Carlos III, Majadahonda, 28220 Madrid, Spain.ORCID 0000-0001-9028-055X
María Josefa RodríguezElectron and Confocal Microscopy Unit, Instituto de Salud Carlos III, Unidades Centrales Científico-Técnicas, Majadahonda, 28220 Madrid, Spain.
María Carmen TerrónElectron and Confocal Microscopy Unit, Instituto de Salud Carlos III, Unidades Centrales Científico-Técnicas, Majadahonda, 28220 Madrid, Spain.
Daniel LuqueElectron and Confocal Microscopy Unit, Instituto de Salud Carlos III, Unidades Centrales Científico-Técnicas, Majadahonda, 28220 Madrid, Spain.
Pilar Pérez-RomeroNational Center for Microbiology, Instituto de Salud Carlos III, Majadahonda, 28220 Madrid, Spain.ORCID 0000-0003-3026-7905
Instituto de Salud Carlos III · ES

Funding

Instituto de Salud Carlos III CD18CIII/00007Instituto de Salud Carlos III PI17CIII-00014 (MPY110/18); PI20CIII-00009 (MPY303/20); DTS18CIII/00006 (MPY127/19)Ministry of Science, Technology and Productive Innovation PTA2017-14233-I
6 · The paper itself

Abstract

Dense bodies (DB) are complex, noninfectious particles produced during CMVinfection containing envelope and tegument proteins that may be ideal candidates as vaccines. Although DB were previously described in fibroblasts, no evidence of DB formation has been shown after propagating CMV in epithelial cells. In the present study, both fibroblast MRC-5 and epithelial ARPE-19 cells were used to study DB production during CMV infection. We demonstrate the formation of epithelial cell-derived DB, mostly located as cytoplasmic inclusions in the perinuclear area of the infected cell. DB were gradient-purified, and the nature of the viral particles was confirmed using CMV-specific immunelabeling. Epithelial cell-derived DB had higher density and more homogeneous size (200-300 nm) compared to fibroblast-derived DB (100-600 nm).In agreement with previous results characterizing DB from CMV-infected fibroblasts, the pp65 tegument protein was predominant in the epithelial cell-derived DB. Our results also suggest that epithelial cells had more CMV capsids in the cytoplasm and had spherical bodies compatible with nucleus condensation (pyknosis) in cells undergoing apoptosis that were not detected in MRC-5 infected cells at the tested time post-infection. Our results demonstrate the formation of DB in CMV-infected ARPE-19 epithelial cells that may be suitable candidate to develop a multiprotein vaccine with antigenic properties similar to that of the virions while not including the viral genome.

Indexed as

cytomegalovirusdense bodiesepithelial cellsTEMvaccine design

Identifiers

PMID36016196
PMCPMC9412340
OpenAlexW4292183920

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.