Evidence map›Paper›PMID 33628442›Full record

ArticleClinical & translational immunology2021

Human neutralising antibodies elicited by SARS-CoV-2 non-D614G variants offer cross-protection against the SARS-CoV-2 D614G variant.

Cheryl Yi-Pin Lee, Siti Naqiah Amrun, Rhonda Sin-Ling Chee, Yun Shan Goh, Tze-Minn Mak, Sophie Octavia, Nicholas Kim-Wah Yeo, Zi Wei Chang, Matthew Zirui Tay, Anthony Torres-Ruesta and 15 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

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  7. Evolution of SARS-CoV-2 neutralizing antibody in an HIV-positive patient with COVID-19.Journal of the Formosan Medical Association = Taiwan yi zhi · 2021
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  14. Molecular characterization of interactions between the D614G variant of SARS-CoV-2 S-protein and neutralizing antibodies: A computational approach.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2021
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  17. Functional importance of the D614G mutation in the SARS-CoV-2 spike protein.Biochemical and biophysical research communications · 2021
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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

25 authors at 5 institutions in 2 countries.

Cheryl Yi-Pin LeeASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Siti Naqiah AmrunASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Rhonda Sin-Ling CheeASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Yun Shan GohASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Tze-Minn MakNational Centre for Infectious Diseases Singapore.
Sophie OctaviaNational Centre for Infectious Diseases Singapore.
Nicholas Kim-Wah YeoASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Zi Wei ChangASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Matthew Zirui TayASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Anthony Torres-RuestaASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Guillaume CarissimoASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Chek Meng PohASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.ORCID https://orcid.org/0000-0003-0059-3937
Siew-Wai FongASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Wang BeiSingapore Immunology Network Agency for Science, Technology and Research (ASTAR) Singapore.
Sandy LeeSingapore Immunology Network Agency for Science, Technology and Research (ASTAR) Singapore.
Barnaby Edward YoungNational Centre for Infectious Diseases Singapore.
Seow-Yen TanDepartment of Infectious Diseases Changi General Hospital Singapore.
Yee-Sin LeoNational Centre for Infectious Diseases Singapore.
David C LyeNational Centre for Infectious Diseases Singapore.
Raymond Tp LinNational Public Health Laboratory National Centre for Infectious Diseases Singapore.
Sebastien Maurer-StrohASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Bernett LeeSingapore Immunology Network Agency for Science, Technology and Research (ASTAR) Singapore.
Cheng-I WangSingapore Immunology Network Agency for Science, Technology and Research (ASTAR) Singapore.
Laurent ReniaASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Lisa Fp NgASTAR Infectious Diseases Labs Agency for Science, Technology and Research (A*STAR) Singapore.
Agency for Science, Technology and Research · SGNational University of Singapore · SGNational Centre for Infectious Diseases · SGChangi General Hospital · SGNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe emergence of a SARS-CoV-2 variant with a point mutation in the spike (S) protein, D614G, has taken precedence over the original Wuhan isolate by May 2020. With an increased infection and transmission rate, it is imperative to determine whether antibodies induced against the D614 isolate may cross-neutralise against the G614 variant.

methodsAntibody profiling against the SARS-CoV-2 S protein of the D614 variant by flow cytometry and assessment of neutralising antibody titres using pseudotyped lentiviruses expressing the SARS-CoV-2 S protein of either the D614 or G614 variant tagged with a luciferase reporter were performed on plasma samples from COVID-19 patients with known D614G status (

resultsProfiling of the anti-SARS-CoV-2 humoral immunity reveals similar neutralisation profiles against both S protein variants, albeit waning neutralising antibody capacity at the later phase of infection. Of clinical importance, patients infected with either the D614 or G614 clade elicited a similar degree of neutralisation against both pseudoviruses, suggesting that the D614G mutation does not impact the neutralisation capacity of the elicited antibodies.

conclusionsCross-reactivity occurs at the functional level of the humoral response on both the S protein variants, which suggests that existing serological assays will be able to detect both D614 and G614 clades of SARS-CoV-2. More importantly, there should be negligible impact towards the efficacy of antibody-based therapies and vaccines that are currently being developed.

Indexed as

cladeCOVID‐19cross‐reactivityD614G variantneutralising antibodiesSARS‐CoV‐2

Identifiers

PMID33628442
PMCPMC7899292
OpenAlexW3129693855

What OpenQuestion holds

Textmetadata
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.