Evidence map›Paper›PMID 38198525›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

High-resolution map of the Fc functions mediated by COVID-19-neutralizing antibodies.

Ida Paciello, Giuseppe Maccari, Elisa Pantano, Emanuele Andreano, Rino Rappuoli

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Ida PacielloMonoclonal Antibody Discovery Lab, Fondazione Toscana Life Sciences, Siena 53100, Italy.
Giuseppe MaccariData Science for Health Lab, Fondazione Toscana Life Sciences, Siena 53100, Italy.
Elisa PantanoMonoclonal Antibody Discovery Lab, Fondazione Toscana Life Sciences, Siena 53100, Italy.
Emanuele AndreanoMonoclonal Antibody Discovery Lab, Fondazione Toscana Life Sciences, Siena 53100, Italy.ORCID 0000-0003-0088-5788
Rino RappuoliDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena 53100, Italy.ORCID 0000-0002-8827-254X
Toscana Life Sciences · ITUniversity of Siena · IT

Funding

EC | ERC | HORIZON EUROPE European Research Council (ERC) 787552Italian Ministry of Health COVID-2020-12371817
6 · The paper itself

Abstract

A growing body of evidence shows that fragment crystallizable (Fc)-dependent antibody effector functions play an important role in protection from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. To unravel the mechanisms that drive these responses, we analyzed the phagocytosis and complement deposition mediated by a panel of 482 human monoclonal antibodies (nAbs) neutralizing the original Wuhan virus, expressed as recombinant IgG1. Our study confirmed that nAbs no longer neutralizing SARS-CoV-2 Omicron variants can retain their Fc functions. Surprisingly, we found that nAbs with the most potent Fc function recognize the N-terminal domain, followed by those targeting class 3 epitopes in the receptor binding domain. Interestingly, nAbs direct against the class 1/2 epitopes in the receptor binding motif, which are the most potent in neutralizing the virus, were the weakest in Fc functions. The divergent properties of the neutralizing and Fc function-mediating antibodies were confirmed by the use of different B cell germlines and by the observation that Fc functions of polyclonal sera differ from the profile observed with nAbs, suggesting that non-neutralizing antibodies also contribute to Fc functions. These data provide a high-resolution picture of the Fc-antibody response to SARS-CoV-2 and suggest that the Fc contribution should be considered for the design of improved vaccines, the selection of therapeutic antibodies, and the evaluation of correlates of protection.

Indexed as

Antibodies, NeutralizingCOVID-19EpitopesHumansSARS-CoV-2Antibodies, NeutralizingEpitopesantibodiesB cell germlinesFc functionSARS-CoV-2

Identifiers

PMID38198525
PMCPMC10801854
OpenAlexW4390691639

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-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.