Further antibody escape by Omicron BA.4 and BA.5 from vaccine and BA.1 serum

Author:

Tuekprakhon Aekkachai,Huo Jiandong,Nutalai Rungtiwa,Dijokaite-Guraliuc Aiste,Zhou Daming,Ginn Helen M.,Selvaraj Muneeswaran,Liu Chang,Mentzer Alexander J.,Supasa Piyada,Duyvesteyn Helen M.E.,Das Raksha,Skelly Donal,Ritter Thomas G.,Amini Ali,Bibi Sagida,Adele Sandra,Johnson Sile Ann,Constantinides Bede,Webster Hermione,Temperton Nigel,Klenerman Paul,Barnes Eleanor,Dunachie Susanna J.,Crook Derrick,Pollard Andrew J,Lambe Teresa,Goulder Philip,Fry Elizabeth E.,Mongkolsapaya Juthathip,Ren Jingshan,Stuart David I.ORCID,Screaton Gavin R, ,

Abstract

SummaryThe Omicron lineage of SARS-CoV-2, first described in November 2021, spread rapidly to become globally dominant and has split into a number of sub-lineages. BA.1 dominated the initial wave but has been replaced by BA.2 in many countries. Recent sequencing from South Africa’s Gauteng region uncovered two new sub-lineages, BA.4 and BA.5 which are taking over locally, driving a new wave. BA.4 and BA.5 contain identical spike sequences and, although closely related to BA.2, contain further mutations in the receptor binding domain of spike. Here, we study the neutralization of BA.4/5 using a range of vaccine and naturally immune serum and panels of monoclonal antibodies. BA.4/5 shows reduced neutralization by serum from triple AstraZeneca or Pfizer vaccinated individuals compared to BA.1 and BA.2. Furthermore, using serum from BA.1 vaccine breakthrough infections there are likewise, significant reductions in the neutralization of BA.4/5, raising the possibility of repeat Omicron infections.

Publisher

Cold Spring Harbor Laboratory

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