Evidence map›Paper›PMID 34673299›Full record

ReviewInternational immunopharmacology2021

Anti-VEGF agents: As appealing targets in the setting of COVID-19 treatment in critically ill patients.

Adeleh Sahebnasagh, Seyed Mohammad Nabavi, Hamid Reza Khayat Kashani, Safieh Abdollahian, Solomon Habtemariam, Aysa Rezabakhsh

Open access · greenAbstract readReview
In one paragraph

Review in International immunopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. VEGF Polymorphisms (International journal of molecular sciences · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Frontiers in pharmacology · 2022
    Article
  17. Observational
  18. Article
  19. 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

6 authors at 6 institutions in 2 countries.

Adeleh SahebnasaghClinical Research Center, Department of Internal Medicine, School of Medicine, North Khorasan University of Medical Sciences, Bojnurd, Iran.
Seyed Mohammad NabaviApplied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Hamid Reza Khayat KashaniImam Hossein Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Safieh AbdollahianDepartment of Nanobiotechnology, New Technologies Research Group, Pasteur Institute, Tehran, Iran.
Solomon HabtemariamPharmacognosy Research Laboratories & Herbal Analysis Services UK, University of Greenwich, Chatham-Maritime, Kent ME4 4TB, UK.
Aysa RezabakhshCardiovascular Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address: rezabakhsha@tbzmed.ac.ir.
Baqiyatallah University of Medical Sciences · IRImam Hossein Hospital · IRNorth Khorasan University of Medical Sciences · IRPasteur Institute of Iran · IRTabriz University of Medical Sciences · IRUniversity of Greenwich · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, the medications used for the severe form of the coronavirus disease-19 (COVID-19) therapy are of particular interest. In this sense, it has been supposed that anti-VEGF compounds would be good candidates in the face of "cytokine storm" and intussuscepted angiogenesis due to having an appreciable anti-inflammatory effect. Therefore, they can be subjected to therapeutic protocols to manage acute respiratory distress syndrome (ARDS). Since the compelling evidence emphasized that VEGFs contribute to the inflammatory process and play a mainstay role in disease pathogenesis, in this review, we aimed to highlight the VEGF's plausible participation in the cytokine storm exacerbation in COVID-19. Next, the recent clinical advances regarding the anti-VEGF medications, including humanized monoclonal antibody, immunosuppressant, a tyrosine kinase inhibitor, and a cytokine inhibitor, have been addressed in the setting of COVID-19 treatment in critically ill patients. Together, retrieving the increased level of VEGF subsets, as well as antagonizing VEGF related receptors, could be helpful for the treatment of COVID-19, especially in those suffering from ARDS.

Indexed as

COVID-19 Drug TreatmentAngiogenesis InhibitorsCOVID-19Critical IllnessHumansReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth FactorsAngiogenesis InhibitorsReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth FactorsAnti-VEGF therapyCOVID-19Critically Ill PatientsInflammationSARS-CoV-2Therapeutic Target

Identifiers

PMID34673299
PMCPMC8519896
OpenAlexW3207259968

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.