Activity of convalescent and vaccine serum against a B.1.1.529 variant SARS-CoV-2 isolate

Author:

Carreño Juan Manuel,Alshammary Hala,Tcheou Johnstone,Singh Gagandeep,Raskin Ariel,Kawabata Hisaaki,Sominsky Levy,Clark Jordan,Adelsberg Daniel C.,Bielak Dominika,Gonzalez-Reiche Ana Silvia,Srivastava Komal,Sordillo Emilia MiaORCID,Bajic Goran,van Bakel HarmORCID,Simon Viviana,Krammer Florian,

Abstract

The B.1.1.529 (Omicron) variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was identified in November of 2021 in South Africa and Botswana as well as in a sample of a traveler from South Africa in Hong Kong.1,2 Since then, B.1.1.529 has been detected in many countries globally. This variant seems to be more infectious than B.1.617.2 (Delta), has already caused super spreader events3 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.2,4-6 Here, we investigated the neutralizing and binding activity of sera from convalescent, mRNA double vaccinated, mRNA boosted as well as 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 strongly reduced levels. Binding to the B.1.1.529 receptor binding domain (RBD) and N-terminal domain (NTD) was reduced in convalescent not vaccinated but was mostly retained in vaccinated individuals.

Publisher

Cold Spring Harbor Laboratory

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