Cited by 204SARS-CoV-2 and COVID-19 ResearchCOVID-19 Clinical Research StudiesCOVID-19 epidemiological studies

Increased immune escape of the new SARS-CoV-2 variant of concern Omicron

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Hu, Jie, Peng, Pai, Cao, Xiaoxia, Wu, Kang, Chen, Juan, Wang, Kai, Tang, Ni, Huang, Ai-long·2022·Cellular & Molecular Immunology

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Research works printed but not linked: 8

  1. Jhun H, Park H-Y, Hisham Y, Song C-S, Kim S. SARS-CoV-2 Delta (B.1.617.2) variant: a unique T478K mutation in receptor binding motif (RBM) of spike gene. Immune Netw. 2021;21:e32.
  2. Hu J, Gao Q, He C, Huang A, Tang N, Wang K. Development of cell-based pseudovirus entry assay to identify potential viral entry inhibitors and neu- tralizing antibodies against SARS-CoV-2. Genes Dis. 2020;7:551-7.
  3. Cong Z, Evans JP, Qu P, Faraone J, Zheng YM, Carlin C, et al. Neutralization and Stability of SARS-CoV-2 Omicron Variant. bioRxiv, 2021; Preprint at https://doi.org/ 10.1101/2021.2012.2016.472934. · DOI
  4. Peng P, Hu J, Deng HJ, Liu BZ, Fang L, Wang K, et al. Changes in the humoral immunity response in SARS-CoV-2 convalescent patients over 8 months. Cell Mol Immunol. 2021;18:490-1.
  5. Chan CW, Hui PY, Tam WC, Poon LLM, Nicholls J. Omicron SARS-CoV-2 can infect faster and better than Delta in human bronchus but with less severe infection in lung. In press (December 15th, 2021). https://www.med.hku.hk/en/news/press/ 20211215-omicron-sars-cov-2-infection.
  6. Syed F, Li W, Relich RF, Russell PM, Zhang S, Zimmerman MK, et al. Omicron mutations enhance infectivity and reduce antibody neutralization of SARS-CoV-2 virus-like particles. medRxiv, 2021; Preprint at https://doi.org/ 10.1101/2021.12.20.21268048. · DOI
  7. Planas D, Saunders N, Maes P, Guivel-Benhassine F, Planchais C, Buchrieser J, et al. Considerable escape of SARS-CoV-2 variant Omicron to antibody neutralization. Nature. 2021;596:276-80.
  8. Tang J, Grubbs G, Lee Y, Huang C, Ravichandran S, Forgacs D, et al. Antibody affinity maturation and cross-variant activity following SARS-CoV-2 mRNA vacci- nation: Impact of prior exposure and sex. EBioMedicine. 2021;74:103748.

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Authors
Hu, J., Peng, P., Cao, X., Wu, K., Chen, J., Wang, K., Tang, N., & Huang, A.-L.
Affiliations
Second Affiliated Hospital of Chongqing Medical University (CN)
Corresponding author
Huang, Ai-long
Venue
Cellular & Molecular Immunology
Published
2022-01-11
Volume
19
Issue
2
Pages
293-295
ISSN
  • 1672-7681 (ISSN-L)
  • 2042-0226
OpenAlex
W4206175278
Cited by
204
References
6
Citations by year
2026: 4 · 2025: 9 · 2024: 29 · 2023: 65 · 2022: 95 · 2021: 1
FWCI
24.32
Type
journal article
Language
en
Open access
Locations
  • Cellular and Molecular Immunology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Natural Science Foundation of China (111 Project, [2021]02, 2021-05, U20A20392, 2017ZX10202203, 82102361, D20028)
  • China Postdoctoral Science Foundation (202102, 2021M693924, 202105, 2017ZX10202203)
  • Chongqing Science and Technology Commission (cstc2020jscx-fyzx0053, CSTCCXLJRC201719)
  • Chongqing Medical University (D20028, 202105, CQMUNCP0302)
  • Natural Science Foundation of Chongqing (cstc2020jscx-fyzx0053, cstc2021jcyj)
  • Chongqing Postdoctoral Science Special Foundation (2010010005216630)
  • Higher Education Discipline Innovation Project (D20028)
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
  • Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
Keywords
Omicron variant, SARS-CoV-2, immune evasion, variants of concern, COVID-19 pandemic, viral evolution, SARS-CoV-2 spike protein
MeSH terms
A549 Cells, Angiotensin-Converting Enzyme 2, COVID-19, SARS-CoV-2, Antibodies, Viral, Humans, Mutation, Transfection, Immune Evasion, Antibodies, Neutralizing, HEK293 Cells, Spike Glycoprotein, Coronavirus

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