Evidence map›Paper›PMID 32244484›Full record

ReviewJournal of clinical medicine2020

Deriving Immune Modulating Drugs from Viruses-A New Class of Biologics.

Jordan R Yaron, Liqiang Zhang, Qiuyun Guo, Michelle Burgin, Lauren N Schutz, Enkidia Awo, Lyn Wise, Kurt L Krause, Cristhian J Ildefonso, Jacek M Kwiecien and 7 more

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. A protracted war against cancer drug resistance.Cancer cell international · 2024
    Review
  4. Biology · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. TNF Decoy Receptors Encoded by Poxviruses.Pathogens (Basel, Switzerland) · 2021
    Review
  10. Attenuation of acute and chronic inflammation using compounds derived from plants.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  11. Review
  12. Therapeutic SERPINs: Improving on Nature.Frontiers in cardiovascular medicine · 2021
    Review
  13. Article
  14. Review
  15. RecombinantPharmaceutics · 2020
    Article
  16. 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

17 authors at 8 institutions in 5 countries.

Jordan R YaronCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Liqiang ZhangCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Qiuyun GuoCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Michelle BurginCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Lauren N SchutzCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Enkidia AwoCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Lyn WiseUniversity of Otago, Dunedin, 9054, New Zealand.
Kurt L KrauseUniversity of Otago, Dunedin, 9054, New Zealand.
Cristhian J IldefonsoDepartment of Ophthalmology, University of Florida, Gainesville, FL 32610, USA.
Jacek M KwiecienDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON L8S4L8, Canada.
Michael JubyCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Masmudur M RahmanCenter for Immunotherapy, Vaccines and Virotherapy, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Hao ChenThe Department of Tumor Surgery, Second Hospital of Lanzhou University, Lanzhou, 730030, China.
Richard W MoyerDepartment of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL 32610, USA.
Antonio AlcamiCentro de Biología Molecular Severo Ochoa (Consejo Superior de Investigaciones Científicas and Universidad Autónoma de Madrid), Cantoblanco, Madrid, 28049, Spain.
Grant McFaddenCenter for Immunotherapy, Vaccines and Virotherapy, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Alexandra R LucasCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Arizona State University · USUniversity of Florida · USUniversity of Otago · NZConsejo Superior de Investigaciones Científicas · ESCreighton University · USLanzhou University Second Hospital · CNMcMaster University · CATongji Hospital · CN

Funding

American Heart Association 17GRNT33460327Biodesign Institute at Arizona State University Start-UpNIH HHS 1R01AI100987-01A1NIH HHS 1RC1HL100202University of Florida Foundation 00115070
6 · The paper itself

Abstract

Viruses are widely used as a platform for the production of therapeutics. Vaccines containing live, dead and components of viruses, gene therapy vectors and oncolytic viruses are key examples of clinically-approved therapeutic uses for viruses. Despite this, the use of virus-derived proteins as natural sources for immune modulators remains in the early stages of development. Viruses have evolved complex, highly effective approaches for immune evasion. Originally developed for protection against host immune responses, viral immune-modulating proteins are extraordinarily potent, often functioning at picomolar concentrations. These complex viral intracellular parasites have "performed the R&D", developing highly effective immune evasive strategies over millions of years. These proteins provide a new and natural source for immune-modulating therapeutics, similar in many ways to penicillin being developed from mold or streptokinase from bacteria. Virus-derived serine proteinase inhibitors (serpins), chemokine modulating proteins, complement control, inflammasome inhibition, growth factors (e.g., viral vascular endothelial growth factor) and cytokine mimics (e.g., viral interleukin 10) and/or inhibitors (e.g., tumor necrosis factor) have now been identified that target central immunological response pathways. We review here current development of virus-derived immune-modulating biologics with efficacy demonstrated in pre-clinical or clinical studies, focusing on pox and herpesviruses-derived immune-modulating therapeutics.

Indexed as

biologicchemokinechemokine binding proteincytokinegrowth factorimmune modulationinterleukinproteinserpintherapeuticvirus

Identifiers

PMID32244484
PMCPMC7230489
OpenAlexW3014571765

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.