The Sato Lab (Kei Sato) Profile picture
Jul 17 8 tweets 2 min read Read on X
BREAKING🔔 Here I want to quickly report our new results from G2P-Japan🇯🇵 before the preprint publication. We have elucidated the virological characteristics of SARS-CoV-2 KP.3.1.1 - a progeny of JN.1. Please RT🔥 1/
Cf.1 A new one, KP.2 (JN.1.11.1.2), has been already elucidated. 2/
Cf.2 Another new ones, KP.3 (JN.1.11.1.3), LB.1 (JN.1.9.2.1) and KP.2.3 (JN.1.11.1.2.3), have also been already elucidated. 3/
Here we focused on a new one, KP.3.1.1 (JN.1.11.1.3.1.1). This variant harbors these mutations.
KP.3.1.1 spike = KP.3 spike + S31del. 4/ Image
Transmissibility/fitness (Re): molecular phylogenetic-epidemic dynamics modeling led by Jumpei @jampei2 and Kaho showed that the Re of KP.3.1.1 is greater than those of the other JN.1 subvariants. 5/ Image
Pseudovirus infectivity: KP.3.1.1 is more infectious than KP.3. 6/ Image
Immune resistance: the 50% neutralization values of breakthrough infection (BTI) sera with XBB.1.5, EG.5.1, HK.3 and JN.1 as well as XBB.1.5 vaccine sera against KP.3.1.1 were significantly lower than those against KP.3 and even KP.2.3 in some cases🔥 7/ Image
These results suggest that KP.3.1.1 has the potential to be predominant, due to its higher infectivity and increased immune evasion. In particular, #S31del in spike, the common mutation in KP.3.1.1, LB.1 and KP.2.3, is likely to be a key mutation. 8/8

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More from @SystemsVirology

Jul 17
#拡散希望 速報🔔 G2P-Japan🇯🇵の新しい研究成果「新型コロナウイルス変異株KP.3.1.1のウイルス学的特性の解明」について、プレプリント公開に先立って速報します。本研究では、最近いくつかの国で増加傾向にある、JN.1の子孫株である新しい変異株KP.3.1.1の特性を検証しました。1/
春になり、JN.1の子孫株が出現し、それらが優勢になり始めています。現在本邦は第11波に入っていますが、それはこれらのJN.1の子孫株によって引き起こされています。現在の流行状況などについては、本日公開の最新コラムで解説しています↓ 2/
そのひとつ、KP.2 (JN.1.11.1.2)については、すでにG2P-Japan🇯🇵が論文として報告しています。3/
Read 10 tweets
Jun 6
#拡散希望 速報🔔 G2P-Japan🇯🇵の新しい研究成果「新型コロナウイルス変異株KP.3, LB.1, KP.2.3のウイルス学的特性の解明」について、プレプリント公開に先立って速報します。本研究では、最近いくつかの国で増加傾向にある、JN.1の子孫株である新しい3つの変異株の特性を検証しました。1/
春になり、JN.1の子孫株が出現し、それらが優勢になり始めています。そのひとつ、KP.2 (JN.1.11.1.2)の特性については、すでにG2P-Japan🇯🇵が論文として報告しています。2/
今回着目したのは、KP.2にやや遅れて出現した3つの株、KP.3 (JN.1.11.1.3)、LB.1 (JN.1.9.2.1)、KP.2.3 (JN.1.11.1.2.3)です。それぞれ、こんな変異を持っています。
(*参考まで、JN.1=BA.2.86.1.1で、BA.2.86系統の子孫株)3/ Image
Read 8 tweets
Jun 6
BREAKING🔔 Here I want to quickly report our new results from G2P-Japan🇯🇵 before the preprint publication. We have elucidated the virological characteristics of SARS-CoV-2 KP.3, LB.1 and KP.2.3 - progeny of JN.1. Please RT🔥 1/
Cf. A new one, KP.2 (JN.1.11.1.2), has been already elucidated. 2/
Here we focused on relatively new ones, KP.3 (JN.1.11.1.3), LB.1 (JN.1.9.2.1) and KP.2.3 (JN.1.11.1.2.3). These variants harbor these mutations⬇️ 3/ Image
Read 7 tweets
May 20
#拡散希望 第2回新型コロナウイルス研究集会を、8月2日〜4日に東京・品川で開催します! 今年のテーマは「COVID-19の疫学、臨床医学、免疫学、ウイルス学」。新型コロナに関する科学のすべてを網羅した集会になるよう準備を進めています! 1/
confit.atlas.jp/guide/event/co…
参加・演題登録はこちらから↓
今年は「オンデマンド配信」も予定しています。先約があったり、遠方で現地参加が難しい方や、医療従事者のみなさまにも広くご参加いただき、新型コロナの科学の最先端を知る機会を提供できればと思っています。2/
confit.atlas.jp/guide/event/co…
今年は、G2P-Japanが基礎ウイルス学を担当し、免疫学を⾼橋宜聖先生(感染研)、臨床医学を忽那賢志先生(阪⼤)@kutsunasatoshi 、公衆衛生学を押⾕仁(東北⼤)に担当いただきます。3/
confit.atlas.jp/guide/event/co…
Read 5 tweets
Apr 27
BREAKING🔔 A new study from G2P-Japan🇯🇵 is out at bioRxiv @biorxivpreprint. We elucidated the virological characteristics of SARS-CoV-2 KP.2 - a progeny of JN.1. Please RT🔥 1/
biorxiv.org/cgi/content/sh…
Cf. This is KP.2 (aka JN.1.11.1.2). In spike, KP.2 = JN.1 + S:R346T, S:F456L & S:V1104L).

We remember that R346T was observed in BQ.1.1 and XBB lineages, while F456L is a hallmark of EG.5 lineage. 2/ Image
Transmissibility/fitness (Re): molecular phylogenetic-epidemic dynamics modeling led by Jumpei @jampei2 and Kaho showed that the Re of KP.2 is ~1.2-fold greater than that of JN.1. 3/
Image
Image
Read 6 tweets
Jan 9
BREAKING🔔 The 32nd paper from G2P-Japan🇯🇵 is out at Lancet Infectious Diseases @TheLancetInfDis. We show the breadth of antisera induced by XBB.1.5 monovalent vaccine - comparison between infection-naïve and XBB-infected individuals. Please repost🔥 1/
thelancet.com/journals/lanin…
To control SARS-CoV-2 infection, the XBB.1.5 monovalent vaccine is now available. However, we found that natural infection with XBB subvariants, including XBB.1.5, does not efficiently induce humoral immunity against the infecting XBB subvariants, e.g. 2/
These observations raise the possibility that the XBB.1.5 monovalent vaccine may not be able to efficiently induce humoral immunity against emerging SARS-CoV-2 variants, including a variety of XBB subvariants as well as BA.2.86 and JN.1. 3/
Read 12 tweets

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