Omicron BA.4/BA.5 escape neutralizing immunity elicited by BA.1 infection

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作者
Khadija Khan
Farina Karim
Yashica Ganga
Mallory Bernstein
Zesuliwe Jule
Kajal Reedoy
Sandile Cele
Gila Lustig
Daniel Amoako
Nicole Wolter
Natasha Samsunder
Aida Sivro
James Emmanuel San
Jennifer Giandhari
Houriiyah Tegally
Sureshnee Pillay
Yeshnee Naidoo
Matilda Mazibuko
Yoliswa Miya
Nokuthula Ngcobo
Nithendra Manickchund
Nombulelo Magula
Quarraisha Abdool Karim
Anne von Gottberg
Salim S. Abdool Karim
Willem Hanekom
Bernadett I. Gosnell
Richard J. Lessells
Tulio de Oliveira
Mahomed-Yunus S. Moosa
Alex Sigal
机构
[1] Africa Health Research Institute,School of Laboratory Medicine and Medical Sciences
[2] University of KwaZulu-Natal,School of Health Sciences, College of Health Sciences
[3] Centre for the AIDS Programme of Research in South Africa,School of Pathology, Faculty of Health Sciences
[4] National Institute for Communicable Diseases of the National Health Laboratory Service,Department of Medical Microbiology
[5] University of KwaZulu-Natal,Centre for Epidemic Response and Innovation (CERI), School of Data Science and Computational Thinking
[6] University of the Witwatersrand,Department of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine
[7] University of KwaZulu-Natal,Division of Internal Medicine, Nelson R. Mandela School of Medicine
[8] KwaZulu-Natal Research Innovation and Sequencing Platform,Department of Epidemiology, Mailman School of Public Health
[9] Stellenbosch University,Division of Infection and Immunity
[10] University of KwaZulu-Natal,Department of Global Health
[11] University of Kwa-Zulu Natal,Division of Infectious Diseases
[12] Columbia University,undefined
[13] University College London,undefined
[14] University of Washington,undefined
[15] Max Planck Institute for Infection Biology,undefined
[16] University of Alabama at Birmingham,undefined
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摘要
SARS-CoV-2 Omicron (B.1.1.529) BA.4 and BA.5 sub-lineages, first detected in South Africa, have changes relative to Omicron BA.1 including substitutions in the spike receptor binding domain. Here we isolated live BA.4 and BA.5 viruses and measured BA.4/BA.5 neutralization elicited by BA.1 infection either in the absence or presence of previous vaccination as well as from vaccination without BA.1 infection. In BA.1-infected unvaccinated individuals, neutralization relative to BA.1 declines 7.6-fold for BA.4 and 7.5-fold for BA.5. In vaccinated individuals with subsequent BA.1 infection, neutralization relative to BA.1 decreases 3.2-fold for BA.4 and 2.6-fold for BA.5. The fold-drop versus ancestral virus neutralization in this group is 4.0-fold for BA.1, 12.9-fold for BA.4, and 10.3-fold for BA.5. In contrast, BA.4/BA.5 escape is similar to BA.1 in the absence of BA.1 elicited immunity: fold-drop relative to ancestral virus neutralization is 19.8-fold for BA.1, 19.6-fold for BA.4, and 20.9-fold for BA.5. These results show considerable escape of BA.4/BA.5 from BA.1 elicited immunity which is moderated with vaccination and may indicate that BA.4/BA.5 may have the strongest selective advantage in evading neutralization relative to BA.1 in unvaccinated, BA.1 infected individuals.
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