Evidence map›Paper›PMID 33584747›Full record

ArticleFrontiers in plant science2020

Development of Plant-Produced Recombinant ACE2-Fc Fusion Protein as a Potential Therapeutic Agent Against SARS-CoV-2.

Konlavat Siriwattananon, Suwimon Manopwisedjaroen, Phongthon Kanjanasirirat, Priyo Budi Purwono, Kaewta Rattanapisit, Balamurugan Shanmugaraj, Duncan R Smith, Suparerk Borwornpinyo, Arunee Thitithanyanont, Waranyoo Phoolcharoen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Therapeutic Fusion Proteins.The AAPS journal · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Frontiers in bioengineering and biotechnology · 2023
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  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 3 institutions in 2 countries.

Konlavat SiriwattananonResearch Unit for Plant-Produced Pharmaceuticals, Chulalongkorn University, Bangkok, Thailand.
Suwimon ManopwisedjaroenDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Phongthon KanjanasiriratExcellence Center for Drug Discovery, Faculty of Science, Mahidol University, Bangkok, Thailand.
Priyo Budi PurwonoDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Kaewta RattanapisitResearch Unit for Plant-Produced Pharmaceuticals, Chulalongkorn University, Bangkok, Thailand.
Balamurugan ShanmugarajResearch Unit for Plant-Produced Pharmaceuticals, Chulalongkorn University, Bangkok, Thailand.
Duncan R SmithInstitute of Molecular Bioscience, Mahidol University, Salaya, Thailand.
Suparerk BorwornpinyoExcellence Center for Drug Discovery, Faculty of Science, Mahidol University, Bangkok, Thailand.
Arunee ThitithanyanontDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Waranyoo PhoolcharoenResearch Unit for Plant-Produced Pharmaceuticals, Chulalongkorn University, Bangkok, Thailand.
Mahidol University · THChulalongkorn University · THAirlangga University · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of coronavirus disease (COVID-19) which has recently emerged as a potential threat to global public health. SARS-CoV-2 is the third known human coronavirus that has huge impact on the human population after SARS-CoV and MERS-CoV. Although some vaccines and therapeutic drugs are currently in clinical trials, none of them are approved for commercial use yet. As with SARS-CoV, SARS-CoV-2 utilizes angiotensin-converting enzyme 2 (ACE2) as the cell entry receptor to enter into the host cell. In this study, we have transiently produced human ACE2 fused with the Fc region of human IgG1 in

Indexed as

ACE2-Fc fusion proteinCOVID-19molecular farmingNicotiana benthamianaplant-produced recombinant proteinSARS-CoV-2

Identifiers

PMID33584747
PMCPMC7874119
OpenAlexW3118542260

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.