Antibody Binding and Angiotensin-Converting Enzyme 2 Binding Inhibition Is Significantly Reduced for Both the BA.1 and BA.2 Omicron Variants. (15th July 2022)
- Record Type:
- Journal Article
- Title:
- Antibody Binding and Angiotensin-Converting Enzyme 2 Binding Inhibition Is Significantly Reduced for Both the BA.1 and BA.2 Omicron Variants. (15th July 2022)
- Main Title:
- Antibody Binding and Angiotensin-Converting Enzyme 2 Binding Inhibition Is Significantly Reduced for Both the BA.1 and BA.2 Omicron Variants
- Authors:
- Junker, Daniel
Becker, Matthias
Wagner, Teresa R
Kaiser, Philipp D
Maier, Sandra
Grimm, Tanja M
Griesbaum, Johanna
Marsall, Patrick
Gruber, Jens
Traenkle, Bjoern
Heinzel, Constanze
Pinilla, Yudi T
Held, Jana
Fendel, Rolf
Kreidenweiss, Andrea
Nelde, Annika
Maringer, Yacine
Schroeder, Sarah
Walz, Juliane S
Althaus, Karina
Uzun, Gunalp
Mikus, Marco
Bakchoul, Tamam
Schenke-Layland, Katja
Bunk, Stefanie
Haeberle, Helene
Göpel, Siri
Bitzer, Michael
Renk, Hanna
Remppis, Jonathan
Engel, Corinna
Franz, Axel R
Harries, Manuela
Kessel, Barbora
Lange, Berit
Strengert, Monika
Krause, Gerard
Zeck, Anne
Rothbauer, Ulrich
Dulovic, Alex
Schneiderhan-Marra, Nicole
… (more) - Abstract:
- Abstract: Background: The rapid emergence of the Omicron variant and its large number of mutations led to its classification as a variant of concern (VOC) by the World Health Organization. Subsequently, Omicron evolved into distinct sublineages (eg, BA.1 and BA.2), which currently represent the majority of global infections. Initial studies of the neutralizing response toward BA.1 in convalescent and vaccinated individuals showed a substantial reduction. Methods: We assessed antibody (immunoglobulin G [IgG]) binding, ACE2 (angiotensin-converting enzyme 2) binding inhibition, and IgG binding dynamics for the Omicron BA.1 and BA.2 variants compared to a panel of VOCs/variants of interest, in a large cohort (N = 352) of convalescent, vaccinated, and infected and subsequently vaccinated individuals. Results: While Omicron was capable of efficiently binding to ACE2, antibodies elicited by infection or immunization showed reduced binding capacities and ACE2 binding inhibition compared to wild type. Whereas BA.1 exhibited less IgG binding compared to BA.2, BA.2 showed reduced inhibition of ACE2 binding. Among vaccinated samples, antibody binding to Omicron only improved after administration of a third dose. Conclusions: Omicron BA.1 and BA.2 can still efficiently bind to ACE2, while vaccine/infection-derived antibodies can bind to Omicron. The extent of the mutations within both variants prevents a strong inhibitory binding response. As a result, both Omicron variants are able toAbstract: Background: The rapid emergence of the Omicron variant and its large number of mutations led to its classification as a variant of concern (VOC) by the World Health Organization. Subsequently, Omicron evolved into distinct sublineages (eg, BA.1 and BA.2), which currently represent the majority of global infections. Initial studies of the neutralizing response toward BA.1 in convalescent and vaccinated individuals showed a substantial reduction. Methods: We assessed antibody (immunoglobulin G [IgG]) binding, ACE2 (angiotensin-converting enzyme 2) binding inhibition, and IgG binding dynamics for the Omicron BA.1 and BA.2 variants compared to a panel of VOCs/variants of interest, in a large cohort (N = 352) of convalescent, vaccinated, and infected and subsequently vaccinated individuals. Results: While Omicron was capable of efficiently binding to ACE2, antibodies elicited by infection or immunization showed reduced binding capacities and ACE2 binding inhibition compared to wild type. Whereas BA.1 exhibited less IgG binding compared to BA.2, BA.2 showed reduced inhibition of ACE2 binding. Among vaccinated samples, antibody binding to Omicron only improved after administration of a third dose. Conclusions: Omicron BA.1 and BA.2 can still efficiently bind to ACE2, while vaccine/infection-derived antibodies can bind to Omicron. The extent of the mutations within both variants prevents a strong inhibitory binding response. As a result, both Omicron variants are able to evade control by preexisting antibodies. Abstract : Using a large diverse cohort of vaccinated and convalescent individuals, we found that Omicron can bind to angiotensin-converting enzyme 2 (ACE2) more efficiently than inhibitory antibodies. Immunoglobulin G binding and inhibition of ACE2 binding were significantly reduced for both BA.1 and BA.2. … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 76:Number 3(2023)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 76:Number 3(2023)
- Issue Display:
- Volume 76, Issue 3 (2023)
- Year:
- 2023
- Volume:
- 76
- Issue:
- 3
- Issue Sort Value:
- 2023-0076-0003-0000
- Page Start:
- e240
- Page End:
- e249
- Publication Date:
- 2022-07-15
- Subjects:
- SARS-CoV-2 -- Omicron -- antibody binding -- multiplex -- variants of concern
Communicable diseases -- Periodicals
616.905 - Journal URLs:
- http://cid.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://www.journals.uchicago.edu/CID/journal ↗
http://www.jstor.org/journals/10584838.html ↗ - DOI:
- 10.1093/cid/ciac498 ↗
- Languages:
- English
- ISSNs:
- 1058-4838
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.293860
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25748.xml