Evidence map›Paper›PMID 27144097›Full record

ArticleAdipocyte

Human cytomegalovirus infection of human adipose-derived stromal/stem cells restricts differentiation along the adipogenic lineage.

K J Zwezdaryk, M B Ferris, A L Strong, C A Morris, B A Bunnell, N V Dhurandhar, J M Gimble, D E Sullivan

Abstract read
In one paragraph

Article in Adipocyte. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Pathways to Severe COVID-19 for People with Obesity.Obesity (Silver Spring, Md.) · 2021
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. HIV Persistence in Adipose Tissue Reservoirs.Current HIV/AIDS reports · 2018
    Review
  13. Article
  14. Review
  15. Review
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

8 authors.

K J ZwezdarykDepartment of Microbiology and Immunology, Tulane University School of Medicine , New Orleans, LA, USA.
M B FerrisDepartment of Microbiology and Immunology, Tulane University School of Medicine , New Orleans, LA, USA.
A L StrongCenter for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine , New Orleans, LA, USA.
C A MorrisDepartment of Microbiology and Immunology, Tulane University School of Medicine , New Orleans, LA, USA.
B A BunnellCenter for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine, New Orleans, LA, USA; Department of Pharmacology, Tulane University School of Medicine, New Orleans, LA, USA.
N V DhurandharDepartment of Nutritional Sciences, Texas Tech University , Lubbock, TX, USA.
J M GimbleCenter for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine, New Orleans, LA, USA; Department of Medicine, Tulane University School of Medicine, New Orleans, LA, USA; Department of Surgery, Tulane University School of Medicine, New Orleans, LA, USA; LaCell LLC, New Orleans, LA, USA.
D E SullivanDepartment of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, LA, USA; Center for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine, New Orleans, LA, USA.

Funding

The role of the CMV-associated reactive oxygen species in age-relatedP20GM103629 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI JAZWINSKI, S MICHAL · 2012 to 2021
$22.4M
NIGMS NIH HHS P20 GM103629
6 · The paper itself

Abstract

Human adipose-derived stromal/stem cells (ASCs) display potential to be used in regenerative stem cell therapies and as treatments for inflammatory and autoimmune disorders. Despite promising use of ASCs as therapeutics, little is known about their susceptibility to infectious agents. In this study, we demonstrate that ASCs are highly susceptible to human cytomegalovirus (HCMV) infection and permissive for replication leading to release of infectious virions. Additionally, many basic ASC functions are inhibited during HCMV infection, such as differentiation and immunomodulatory potential. To our knowledge this is the first study examining potential adverse effects of HCMV infection on ASC biology. Our results suggest, that an active HCMV infection during ASC therapy may result in a poor clinical outcome due to interference by the virus.

Indexed as

Adipogenesis; adipose stem cell; cytomegalovirus; herpesvirus

Identifiers

PMID27144097
PMCPMC4836472

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.