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SARS-CoV-2 Omicron-B.1.1.529 leads to widespread escape from neutralizing antibody responses

📅 January 3, 2022 👤 Wanwisa Dejnirattisai, Jiandong Huo, Daming Zhou et al. 📖 Cell 📊 1,017 citations

🤖 Plain-English Summary

November 2021, the sequence of a new SARS-CoV-2 viral isolate Omicron-B.1.1.529 was announced, containing far more mutations in Spike (S) than previously reported variants. Omicron S has structural changes from earlier viruses and uses mutations that confer tight binding to ACE2 to unleash evolution driven by immune escape.

🔑 Key Findings

  • Neutralization titers of Omicron by sera from vaccinees and convalescent subjects infected with early pandemic Alpha, Beta, Gamma, or Delta are substantially reduced, or the sera failed to neutralize.
  • Titers against Omicron are boosted by third vaccine doses and are high in both vaccinated individuals and those infected by Delta.
  • Mutations in Omicron knock out or substantially reduce neutralization by most of the large panel of potent monoclonal antibodies and antibodies under commercial development.

💡 Why This Matters

Understanding this could lead to better treatments, improved diagnostics, or a deeper grasp of how the human body works — benefiting patient care globally.

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📋 Article Details

Category 🧬 Medicine & Biology
Published Jan 03, 2022
Journal Cell
Authors Wanwisa Dejnirattisai, Jiandong Huo, Daming Zhou, Jiří Zahradník, Piyada Supasa
DOI 10.1016/j.cell.2021.12.046
Citations 1,017
Source OpenAlex

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