Evidence map›Paper›PMID 38627386›Full record

ArticleNature communications2024

Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection.

Chang Liu, Raksha Das, Aiste Dijokaite-Guraliuc, Daming Zhou, Alexander J Mentzer, Piyada Supasa, Muneeswaran Selvaraj, Helen M E Duyvesteyn, Thomas G Ritter, Nigel Temperton and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.8field-weighted citation impact, top 3% of its field
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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Monoclonal Antibodies Targeting Bacterial Infections: A Broad Review of the Field.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 3 countries.

Chang Liu *Chinese Academy of Medical Science (CAMS) Oxford Institute (COI), University of Oxford, Oxford, UK.ORCID http://orcid.org/0009-0008-8169-4572
Raksha Das *Nuffield Department of Medicine, Centre for Human Genetics, University of Oxford, Oxford, UK.
Aiste Dijokaite-Guraliuc *Nuffield Department of Medicine, Centre for Human Genetics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-4850-9709
Daming Zhou *Chinese Academy of Medical Science (CAMS) Oxford Institute (COI), University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-7188-5243
Alexander J MentzerNuffield Department of Medicine, Centre for Human Genetics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-4502-2209
Piyada SupasaNuffield Department of Medicine, Centre for Human Genetics, University of Oxford, Oxford, UK.
Muneeswaran SelvarajNuffield Department of Medicine, Centre for Human Genetics, University of Oxford, Oxford, UK.
Helen M E DuyvesteynDivision of Structural Biology, Nuffield Department of Medicine, University of Oxford, The Wellcome Centre for Human Genetics, Oxford, UK.
Thomas G RitterOxford University Hospitals NHS Foundation Trust, Oxford, UK.ORCID http://orcid.org/0000-0002-3153-342X
Nigel TempertonViral Pseudotype Unit, Medway School of Pharmacy, University of Kent and Greenwich Chatham Maritime, Kent, ME4 4TB, UK.ORCID http://orcid.org/0000-0002-7978-3815
Paul KlenermanOxford University Hospitals NHS Foundation Trust, Oxford, UK.
Susanna J DunachieOxford University Hospitals NHS Foundation Trust, Oxford, UK.ORCID http://orcid.org/0000-0001-5665-6293
Neil G PatersonDiamond Light Source Ltd, Harwell Science & Innovation Campus, Didcot, UK.ORCID http://orcid.org/0000-0003-4292-6971
Mark A WilliamsDiamond Light Source Ltd, Harwell Science & Innovation Campus, Didcot, UK.ORCID http://orcid.org/0000-0001-9031-9725
David R HallDiamond Light Source Ltd, Harwell Science & Innovation Campus, Didcot, UK.ORCID http://orcid.org/0000-0002-5333-6136
Elizabeth E FryDivision of Structural Biology, Nuffield Department of Medicine, University of Oxford, The Wellcome Centre for Human Genetics, Oxford, UK. liz@strubi.ox.ac.uk.ORCID http://orcid.org/0000-0001-9754-5303
Juthathip MongkolsapayaChinese Academy of Medical Science (CAMS) Oxford Institute (COI), University of Oxford, Oxford, UK. juthathip.mongkolsapaya@well.ox.ac.uk.ORCID http://orcid.org/0000-0003-3416-9480
Jingshan RenDivision of Structural Biology, Nuffield Department of Medicine, University of Oxford, The Wellcome Centre for Human Genetics, Oxford, UK. ren@strubi.ox.ac.uk.ORCID http://orcid.org/0000-0003-4015-1404
David I StuartChinese Academy of Medical Science (CAMS) Oxford Institute (COI), University of Oxford, Oxford, UK. dave@strubi.ox.ac.uk.ORCID http://orcid.org/0000-0002-3426-4210
Gavin R ScreatonChinese Academy of Medical Science (CAMS) Oxford Institute (COI), University of Oxford, Oxford, UK. gavin.screaton@medsci.ox.ac.uk.ORCID http://orcid.org/0000-0002-3549-4309
Centre for Human Genetics · GBDiamond Light Source · GBUniversity of Oxford · GBMedway School of Pharmacy · GBOxford University Hospitals NHS Trust · GB

Funding

Medical Research Council MC_PC_19059Medical Research Council MR/N00065X/1Medical Research Council MR/X009297/1Wellcome Trust
6 · The paper itself

Abstract

The rapid evolution of SARS-CoV-2 is driven in part by a need to evade the antibody response in the face of high levels of immunity. Here, we isolate spike (S) binding monoclonal antibodies (mAbs) from vaccinees who suffered vaccine break-through infections with Omicron sub lineages BA.4 or BA.5. Twenty eight potent antibodies are isolated and characterised functionally, and in some cases structurally. Since the emergence of BA.4/5, SARS-CoV-2 has continued to accrue mutations in the S protein, to understand this we characterize neutralization of a large panel of variants and demonstrate a steady attrition of neutralization by the panel of BA.4/5 mAbs culminating in total loss of function with recent XBB.1.5.70 variants containing the so-called 'FLip' mutations at positions 455 and 456. Interestingly, activity of some mAbs is regained on the recently reported variant BA.2.86.

Indexed as

Antibodies, MonoclonalPostoperative ComplicationsAntibodies, NeutralizingAntibodies, ViralHumansMutationSARS-CoV-2Antibodies, MonoclonalAntibodies, NeutralizingAntibodies, Viral

Identifiers

PMID38627386
PMCPMC11021415
OpenAlexW4394844415

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.