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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  kyouindb  KAKEN_id  orcid 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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