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ファイル | 記述 | サイズ | フォーマット | |
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j.virol.2024.110067.pdf | 2.03 MB | Adobe PDF | 見る/開く |
タイトル: | Neutralization sensitivity of FL.1 and GE.1 from therapeutic antibodies and seropositive XBB sera |
著者: | Lee, Joseph Naoe, Youichi Bang, Uikyu Nakagama, Yu Saito, Akatsuki Kido, Yasutoshi Hotta, Akitsu https://orcid.org/0000-0002-2619-7441 (unconfirmed) |
著者名の別形: | リー, ジョセフ 直江, 洋一 パン, イギュ 堀田, 秋津 |
キーワード: | SARS-CoV-2 Omicron Spike XBB EG.5 FL.1 GE.1 Neutralization Humoral immunity |
発行日: | Jul-2024 |
出版者: | Elsevier BV |
誌名: | Virology |
巻: | 595 |
論文番号: | 110067 |
抄録: | Two SARS-CoV-2 XBB sub-variants, FL.1 and GE.1, have been increasing in prevalence worldwide, but limited information is available about their ability to evade the immune system. FL.1 and GE.1 are emerging Omicron XBB variants possessing additional mutations in the spike RBD raising concerns of increased neutralization escape. In this study, we assessed the neutralizing ability of eleven FDA-approved monoclonal antibody combinations against different Omicron variants, including BA.2.75, BA.2.76, BA.4/5, XBB.1.5, and CH.1.1. Among the eleven antibodies, Sotrovimab was the only antibody to show broad neutralization ability against XBB.1.5. However, Sotrovimab showed attenuated neutralization efficiency against recently emerging XBB sub-lineages EG.5, FL.1, and GE.1 compared to XBB.1.5. Additionally, XBB.1.5 seropositive convalescent sera displayed lower neutralization activity against EG.5, FL.1, and GE.1. Overall, our findings present enhanced immune evasion capacity of emerging XBB variants and emphasize the importance of continued monitoring of novel variants. |
著作権等: | © 2024 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license. |
URI: | http://hdl.handle.net/2433/290306 |
DOI(出版社版): | 10.1016/j.virol.2024.110067 |
PubMed ID: | 38653156 |
出現コレクション: | 学術雑誌掲載論文等 |
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