Evidence map›Paper›PMID 34909788›Full record

ArticlemedRxiv : the preprint server for health sciences2021

SARS-CoV-2 Omicron has extensive but incomplete escape of Pfizer BNT162b2 elicited neutralization and requires ACE2 for infection.

Sandile Cele, Laurelle Jackson, David S Khoury, Khadija Khan, Thandeka Moyo-Gwete, Houriiyah Tegally, James Emmanuel San, Deborah Cromer, Cathrine Scheepers, Daniel Amoako and 24 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 361 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 9 institutions in 5 countries.

Sandile CeleAfrica Health Research Institute, Durban, South Africa.
Laurelle JacksonAfrica Health Research Institute, Durban, South Africa.
David S KhouryKirby Institute, University of New South Wales, Sydney, Australia.
Khadija KhanAfrica Health Research Institute, Durban, South Africa.
Thandeka Moyo-GweteNational Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Houriiyah TegallyKwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
James Emmanuel SanKwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
Deborah CromerKirby Institute, University of New South Wales, Sydney, Australia.
Cathrine ScheepersNational Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Daniel AmoakoNational Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Farina KarimAfrica Health Research Institute, Durban, South Africa.
Mallory BernsteinAfrica Health Research Institute, Durban, South Africa.
Gila LustigCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.
Derseree ArcharyCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.
Muneerah SmithDepartment of Integrative Biomedical Sciences, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Yashica GangaAfrica Health Research Institute, Durban, South Africa.
Zesuliwe JuleAfrica Health Research Institute, Durban, South Africa.
Kajal ReedoyAfrica Health Research Institute, Durban, South Africa.
Shi-Hsia HwaAfrica Health Research Institute, Durban, South Africa.
Jennifer GiandhariKwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
Jonathan M BlackburnDepartment of Integrative Biomedical Sciences, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Bernadett I GosnellDepartment of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal, Durban, South Africa.
Salim S Abdool KarimCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.
Willem HanekomAfrica Health Research Institute, Durban, South Africa.
NGS-SA
COMMIT-KZN Team
Anne von GottbergNational Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Jinal BhimanNational Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Richard J LessellsKwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
Mahomed-Yunus S MoosaDepartment of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal, Durban, South Africa.
Miles P DavenportKirby Institute, University of New South Wales, Sydney, Australia.
Tulio de OliveiraKwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
Penny L MooreNational Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Alex SigalAfrica Health Research Institute, Durban, South Africa.
Africa Health Research Institute · ZANational Health Laboratory Service · ZACentre for the AIDS Programme of Research in South Africa · ZAStellenbosch University · ZAUniversity of Cape Town · ZAUniversity of Washington · USUNSW Sydney · AUMax Planck Institute for Infection Biology · DEUniversity of KwaZulu-Natal · ZA

Funding

Identification of the HIV Reservoir in Lymph Nodes Using Single Cell RNA-SeqR01AI138546 · NIAID · KWAZULU-NATAL RESEARCH INSTITUTE TB-HIV · PI SIGAL, ALEXANDER · 2018 to 2022
$721k
NIAID NIH HHS R01 AI138546Wellcome Trust
6 · The paper itself

Abstract

The emergence of SARS-CoV-2 Omicron, first identified in Botswana and South Africa, may compromise vaccine effectiveness and the ability of antibodies triggered by previous infection to protect against re-infection (1). Here we investigated whether Omicron escapes antibody neutralization in South Africans, either previously SARS-CoV-2 infected or uninfected, who were vaccinated with Pfizer BNT162b2. We also investigated if Omicron requires the ACE2 receptor to infect cells. We isolated and sequence confirmed live Omicron virus from an infected person in South Africa and compared plasma neutralization of this virus relative to an ancestral SARS-CoV-2 strain with the D614G mutation, observing that Omicron still required ACE2 to infect. For neutralization, blood samples were taken soon after vaccination, so that vaccine elicited neutralization was close to peak. Neutralization capacity of the D614G virus was much higher in infected and vaccinated versus vaccinated only participants but both groups had 22-fold Omicron escape from vaccine elicited neutralization. Previously infected and vaccinated individuals had residual neutralization predicted to confer 73% protection from symptomatic Omicron infection, while those without previous infection were predicted to retain only about 35%. Both groups were predicted to have substantial protection from severe disease. These data support the notion that high neutralization capacity elicited by a combination of infection and vaccination, and possibly boosting, could maintain reasonable effectiveness against Omicron. A waning neutralization response is likely to decrease vaccine effectiveness below these estimates. However, since protection from severe disease requires lower neutralization levels and involves T cell immunity, such protection may be maintained.

Identifiers

PMID34909788
PMCPMC8669855
OpenAlexW4200317137

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.