Evidence map›Paper›PMID 41299695›Full record

ReviewVirology journal2025

The virology of Omicron: pathophysiology, immune regulation, and clinical impact of SARS-CoV-2 sub variants.

Nistha Mishra, Tanya Goel, Nisarg Gangani, Heerak Chugh, Bhavesh Kevadiya, Manisha Tiwari, Snigdha Singh, Jai Gopal Sharma, Ramesh Chandra

Abstract readReview
In one paragraph

Review in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Observational
  5. 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

9 authors.

Nistha Mishra *Drug Discovery and Development Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India.
Tanya Goel *Drug Discovery and Development Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India.
Nisarg GanganiFaculty of Health Sciences, Queen's University, Kingston, ON, Canada.
Heerak ChughDrug Discovery and Development Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India.
Bhavesh KevadiyaDepartment of Radiology, School of Medicine, Stanford University, Palo Alto, CA, USA.
Manisha TiwariDr. B. R. Ambedkar Center for Biomedical Research, University of Delhi, Delhi, 110007, India.
Snigdha SinghDrug Discovery and Development Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India. ssingh3@chemistry.du.ac.in.
Jai Gopal SharmaDepartment of Biotechnology, Delhi Technological University, Delhi, 110042, India. sharmajaigopal@yahoo.com.
Ramesh ChandraDrug Discovery and Development Laboratory, Department of Chemistry, University of Delhi, Delhi, 110007, India. rchandra@chemistry.du.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since its emergence in late 2019, SARS-CoV-2 has evolved into multiple variants with distinct genetic and clinical features. Among them, the Omicron variant (B.1.1.529) and its sublineages BA.2.75, JN.1.8, and KP.2 have shown enhanced transmissibility and immune evasion, while generally exhibiting reduced lower respiratory tract pathogenicity compared to earlier variants, thereby continuing to pose significant challenges to public health. In India, these variants have significantly shaped the trajectory of the pandemic, necessitating focused evaluation of their biological and clinical impact. This review aims to provide a comprehensive study on the virology, pathophysiology, and systemic manifestations of Omicron and its emerging subvariants upto July 2025. We discuss their mechanisms of entry and replication, interaction with ACE2 and TMPRSS2 receptors, and evasion of host immune responses. Particular emphasis is placed on multi-organ involvement beyond the respiratory system, including neuro-respiratory dysregulation, cardiovascular complications, hepatic injury, gastrointestinal disturbances, and renal dysfunction. Furthermore, we evaluate the effectiveness of available vaccines, antiviral therapies, and diagnostic tools, alongside emerging clinical strategies such as vagus nerve stimulation, thermal modulation, and respiratory muscle training. By integrating molecular insights with clinical outcomes, this review highlights the multifaceted and systemic nature of Omicron-induced disease. We underscore the urgent need for variant-specific immunisation, early intervention strategies, and robust genomic surveillance to mitigate long-term sequelae and guide preparedness for future outbreaks.

Indexed as

COVID-19SARS-CoV-2Angiotensin-Converting Enzyme 2Evolution, MolecularHumansImmune EvasionIndiaSerine EndopeptidasesVirus InternalizationACE2 protein, humanAngiotensin-Converting Enzyme 2Serine EndopeptidasesTMPRSS2 protein, humanCovid-19MutationOmicronSARS-CoV-2TransmissibilityVaccines

Identifiers

PMID41299695
PMCPMC12750824

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.