Evidence map›Paper›PMID 33816521›Full record

ReviewFrontiers in medicine2021

Combination of Angiotensin (1-7) Agonists and Convalescent Plasma as a New Strategy to Overcome Angiotensin Converting Enzyme 2 (ACE2) Inhibition for the Treatment of COVID-19.

Hawraa Issa, Ali H Eid, Bassam Berry, Vahideh Takhviji, Abbas Khosravi, Sarah Mantash, Rawan Nehme, Rawan Hallal, Hussein Karaki, Kawthar Dhayni and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  6. Potency of Xanthone Derivatives fromMolecules (Basel, Switzerland) · 2023
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  9. Journal of inflammation research · 2023
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  13. Molecular and pro-inflammatory aspects of COVID-19: The impact on cardiometabolic health.Biochimica et biophysica acta. Molecular basis of disease · 2022
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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

14 authors at 7 institutions in 5 countries.

Hawraa IssaPRASE and Biology Department, Faculty of Sciences - I, Lebanese University, Beirut, Lebanon.
Ali H EidDepartment of Basic Medical Sciences, College of Medicine, QU Health, Qatar University, Doha, Qatar.
Bassam BerryInstitut Pasteur, Paris 6 University, Paris, France.
Vahideh TakhvijiTransfusion Research Center, High Institute for Research and Education in Transfusion, Tehran, Iran.
Abbas KhosraviTransfusion Research Center, High Institute for Research and Education in Transfusion, Tehran, Iran.
Sarah MantashPRASE and Biology Department, Faculty of Sciences - I, Lebanese University, Beirut, Lebanon.
Rawan NehmePRASE and Biology Department, Faculty of Sciences - I, Lebanese University, Beirut, Lebanon.
Rawan HallalPRASE and Biology Department, Faculty of Sciences - I, Lebanese University, Beirut, Lebanon.
Hussein KarakiPRASE and Biology Department, Faculty of Sciences - I, Lebanese University, Beirut, Lebanon.
Kawthar DhayniPRASE and Biology Department, Faculty of Sciences - I, Lebanese University, Beirut, Lebanon.
Wissam H FaourSchool of Medicine, Lebanese American University, Byblos, Lebanon.
Firas KobeissyDepartment of Biochemistry and Molecular Genetics, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.
Ali NehmeDepartment of Human Genetics, McGill University, Montreal, QC, Canada.
Kazem ZibaraPRASE and Biology Department, Faculty of Sciences - I, Lebanese University, Beirut, Lebanon.
Lebanese University · LBHigh Institute for Education and Research in Transfusion Medicine · IRAmerican University of Beirut · LBInstitut Pasteur · FRLebanese American University · LBMcGill University · CAQatar University · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease-2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently the most concerning health problem worldwide. SARS-CoV-2 infects cells by binding to angiotensin-converting enzyme 2 (ACE2). It is believed that the differential response to SARS-CoV-2 is correlated with the differential expression of ACE2. Several reports proposed the use of ACE2 pharmacological inhibitors and ACE2 antibodies to block viral entry. However, ACE2 inhibition is associated with lung and cardiovascular pathology and would probably increase the pathogenesis of COVID-19. Therefore, utilizing ACE2 soluble analogs to block viral entry while rescuing ACE2 activity has been proposed. Despite their protective effects, such analogs can form a circulating reservoir of the virus, thus accelerating its spread in the body. Levels of ACE2 are reduced following viral infection, possibly due to increased viral entry and lysis of ACE2 positive cells. Downregulation of ACE2/Ang (1-7) axis is associated with Ang II upregulation. Of note, while Ang (1-7) exerts protective effects on the lung and cardiovasculature, Ang II elicits pro-inflammatory and pro-fibrotic detrimental effects by binding to the angiotensin type 1 receptor (AT1R). Indeed, AT1R blockers (ARBs) can alleviate the harmful effects associated with Ang II upregulation while increasing ACE2 expression and thus the risk of viral infection. Therefore, Ang (1-7) agonists seem to be a better treatment option. Another approach is the transfusion of convalescent plasma from recovered patients with deteriorated symptoms. Indeed, this appears to be promising due to the neutralizing capacity of anti-COVID-19 antibodies. In light of these considerations, we encourage the adoption of Ang (1-7) agonists and convalescent plasma conjugated therapy for the treatment of COVID-19 patients. This therapeutic regimen is expected to be a safer choice since it possesses the proven ability to neutralize the virus while ensuring lung and cardiovascular protection through modulation of the inflammatory response.

Indexed as

ACE2Angiotensin 1-7 (Ang1-7)cardiovascular pathologycombination therapyconvalescent plasma (CP)COVID-19lung pathologySARS-CoV-2

Identifiers

PMID33816521
PMCPMC8012486
OpenAlexW3136913962

What OpenQuestion holds

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LicenceCC BY
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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.