tetano
Editor, Senior Moderator
Nature
. 2021 Dec 31.
doi: 10.1038/s41586-022-04399-5. Online ahead of print.
Activity of convalescent and vaccine serum against SARS-CoV-2 Omicron
Juan Manuel Carreño[SUP] 1 [/SUP], Hala Alshammary[SUP] 1 [/SUP], Johnstone Tcheou[SUP] 1 [/SUP], Gagandeep Singh[SUP] 1 [/SUP], Ariel Raskin[SUP] 1 [/SUP], Hisaaki Kawabata[SUP] 1 [/SUP], Levy Sominsky[SUP] 1 [/SUP], Jordan Clark[SUP] 1 [/SUP], Daniel C Adelsberg[SUP] 1 [/SUP], Dominika Bielak[SUP] 1 [/SUP], Ana Silvia Gonzalez-Reiche[SUP] 2 [/SUP], Nicholas Dambrauskas[SUP] 3 [/SUP], Vladimir Vigdorovich[SUP] 3 [/SUP], PSP/PARIS Study Group; Komal Srivastava[SUP] 1 [/SUP], D Noah Sather[SUP] 3 4 [/SUP], Emilia Mia Sordillo[SUP] 5 [/SUP], Goran Bajic[SUP] 6 [/SUP], Harm van Bakel[SUP] 7 [/SUP], Viviana Simon[SUP] 8 9 10 11 [/SUP], Florian Krammer[SUP] 12 13 [/SUP]
Collaborators, Affiliations
Abstract
The Omicron (B.1.1.529) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was initially identified in November of 2021 in South Africa and Botswana as well as in a sample from a traveler from South Africa in Hong Kong[SUP]1,2[/SUP]. Since then, B.1.1.529 has been detected globally. This variant seems to be at least equally infectious than B.1.617.2 (Delta), has already caused super spreader events[SUP]3[/SUP] and has outcompeted Delta within weeks in several countries and metropolitan areas. B.1.1.529 hosts an unprecedented number of mutations in its spike gene and early reports have provided evidence for extensive immune escape and reduced vaccine effectiveness[SUP]2,4-6[/SUP]. Here, we investigated the neutralizing and binding activity of sera from convalescent, mRNA double vaccinated, mRNA boosted, convalescent double vaccinated, and convalescent boosted individuals against wild type, B.1.351 and B.1.1.529 SARS-CoV-2 isolates. Neutralizing activity of sera from convalescent and double vaccinated participants was undetectable to very low against B.1.1.529 while neutralizing activity of sera from individuals who had been exposed to spike three or four times was maintained, albeit at significantly reduced levels. Binding to the B.1.1.529 receptor binding domain (RBD) and N-terminal domain (NTD) was reduced in convalescent not vaccinated individuals, but was mostly retained in vaccinated individuals.
. 2021 Dec 31.
doi: 10.1038/s41586-022-04399-5. Online ahead of print.
Activity of convalescent and vaccine serum against SARS-CoV-2 Omicron
Juan Manuel Carreño[SUP] 1 [/SUP], Hala Alshammary[SUP] 1 [/SUP], Johnstone Tcheou[SUP] 1 [/SUP], Gagandeep Singh[SUP] 1 [/SUP], Ariel Raskin[SUP] 1 [/SUP], Hisaaki Kawabata[SUP] 1 [/SUP], Levy Sominsky[SUP] 1 [/SUP], Jordan Clark[SUP] 1 [/SUP], Daniel C Adelsberg[SUP] 1 [/SUP], Dominika Bielak[SUP] 1 [/SUP], Ana Silvia Gonzalez-Reiche[SUP] 2 [/SUP], Nicholas Dambrauskas[SUP] 3 [/SUP], Vladimir Vigdorovich[SUP] 3 [/SUP], PSP/PARIS Study Group; Komal Srivastava[SUP] 1 [/SUP], D Noah Sather[SUP] 3 4 [/SUP], Emilia Mia Sordillo[SUP] 5 [/SUP], Goran Bajic[SUP] 6 [/SUP], Harm van Bakel[SUP] 7 [/SUP], Viviana Simon[SUP] 8 9 10 11 [/SUP], Florian Krammer[SUP] 12 13 [/SUP]
Collaborators, Affiliations
- PMID: 35016197
- DOI: 10.1038/s41586-022-04399-5
Abstract
The Omicron (B.1.1.529) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was initially identified in November of 2021 in South Africa and Botswana as well as in a sample from a traveler from South Africa in Hong Kong[SUP]1,2[/SUP]. Since then, B.1.1.529 has been detected globally. This variant seems to be at least equally infectious than B.1.617.2 (Delta), has already caused super spreader events[SUP]3[/SUP] and has outcompeted Delta within weeks in several countries and metropolitan areas. B.1.1.529 hosts an unprecedented number of mutations in its spike gene and early reports have provided evidence for extensive immune escape and reduced vaccine effectiveness[SUP]2,4-6[/SUP]. Here, we investigated the neutralizing and binding activity of sera from convalescent, mRNA double vaccinated, mRNA boosted, convalescent double vaccinated, and convalescent boosted individuals against wild type, B.1.351 and B.1.1.529 SARS-CoV-2 isolates. Neutralizing activity of sera from convalescent and double vaccinated participants was undetectable to very low against B.1.1.529 while neutralizing activity of sera from individuals who had been exposed to spike three or four times was maintained, albeit at significantly reduced levels. Binding to the B.1.1.529 receptor binding domain (RBD) and N-terminal domain (NTD) was reduced in convalescent not vaccinated individuals, but was mostly retained in vaccinated individuals.