Evidence map›Paper›PMID 35228064›Full record

ReviewBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie2022

There is nothing exempt from the peril of mutation - The Omicron spike.

Tapan Behl, Ishnoor Kaur, Aayush Sehgal, Sukhbir Singh, Neelam Sharma, Md Khalid Anwer, Hafiz A Makeen, Mohammed Albratty, Hassan A Alhazmi, Saurabh Bhatia and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
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  9. Plants (Basel, Switzerland) · 2022
    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

11 authors at 5 institutions in 4 countries.

Tapan BehlChitkara College of Pharmacy, Chitkara University, Punjab, India. Electronic address: tapan.behl@chitkara.edu.in.
Ishnoor KaurChitkara College of Pharmacy, Chitkara University, Punjab, India.
Aayush SehgalChitkara College of Pharmacy, Chitkara University, Punjab, India.
Sukhbir SinghChitkara College of Pharmacy, Chitkara University, Punjab, India.
Neelam SharmaChitkara College of Pharmacy, Chitkara University, Punjab, India.
Md Khalid AnwerDepartment of Pharmaceutics, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia.
Hafiz A MakeenPharmacy Practice Research Unit, Clinical Pharmacy Department, College of Pharmacy, Jazan University, Jazan, Saudi Arabia.
Mohammed AlbrattyDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jazan University, Jazan, Saudi Arabia.
Hassan A AlhazmiDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jazan University, Jazan, Saudi Arabia; Substance Abuse and Toxicology Research Centre, Jazan University, Jazan, Saudi Arabia.
Saurabh BhatiaNatural & Medical Sciences Research Centre, University of Nizwa, Nizwa, Oman; School of Health Science, University of Petroleum and Energy Studies, Dehradun, Uttarakhand, India.
Simona BungauDepartment of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania. Electronic address: simonabngau@gmail.com.
Chitkara University · INJazan University · SAPrince Sattam Bin Abdulaziz University · SAUniversity of Oradea · ROUniversity of Petroleum and Energy Studies · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 2019 corona virus disease (COVID-19) has caused a global chaos, where a novel Omicron variant has challenged the healthcare system, followed by which it has been referred to as a variant of concern (VOC) by the World Health Organization (WHO), owing to its alarming transmission and infectivity rate. The large number of mutations in the receptor binding domain (RBD) of the spike protein is responsible for strengthening of the spike-angiotensin-converting enzyme 2 (ACE2) interaction, thereby explaining the elevated threat. This is supplemented by enhanced resistance of the variant towards pre-existing antibodies approved for the COVID-19 therapy. The manuscript brings into light failure of existing therapies to provide the desired effect, however simultaneously discussing the novel possibilities on the verge of establishing suitable treatment portfolio. The authors entail the risks associated with omicron resistance against antibodies and vaccine ineffectiveness on one side, and novel approaches and targets - kinase inhibitors, viral protease inhibitors, phytoconstituents, entry pathways - on the other. The manuscript aims to provide a holistic picture about the Omicron variant, by providing comprehensive discussions related to multiple aspects of the mutated spike variant, which might aid the global researchers and healthcare experts in finding an optimised solution to this pandemic.

Indexed as

Angiotensin-Converting Enzyme 2AnimalsCathepsinsCOVID-19COVID-19 VaccinesErbB ReceptorsHumansImmunization ScheduleImmunization, SecondaryPhytotherapyPlants, MedicinalProtein BindingProtein Interaction Domains and MotifsProtein Structural ElementsSARS-CoV-2Spike Glycoprotein, CoronavirusAngiotensin-Converting Enzyme 2CathepsinsCOVID-19 VaccinesErbB ReceptorsSpike Glycoprotein, CoronavirusViral Protease InhibitorsACE2Corona virusOmicronReceptor binding domainSpikeVariant of concern

Identifiers

PMID35228064
PMCPMC8872818
OpenAlexW4214645426

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.