Evidence map›Paper›PMID 37011197›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Subclass-switched anti-spike IgG3 oligoclonal cocktails strongly enhance Fc-mediated opsonization.

Arman Izadi, Arsema Hailu, Magdalena Godzwon, Sebastian Wrighton, Berit Olofsson, Tobias Schmidt, Anna Söderlund-Strand, Elizabeth Elder, Sofia Appelberg, Maria Valsjö and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–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

17 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Arman IzadiDepartment of Clinical Sciences Lund, Division of Infection Medicine, Faculty of Medicine, Lund University, 221 84 Lund, Sweden.ORCID 0000-0002-0262-1017
Arsema HailuDepartment of Clinical Sciences Lund, Division of Infection Medicine, Faculty of Medicine, Lund University, 221 84 Lund, Sweden.
Magdalena GodzwonDepartment of Immunotechnology, Faculty of Engineering, Lund University, 221 00 Lund, Sweden.ORCID 0000-0002-9745-1160
Sebastian WrightonDepartment of Clinical Sciences Lund, Division of Infection Medicine, Faculty of Medicine, Lund University, 221 84 Lund, Sweden.ORCID 0000-0002-3378-7925
Berit OlofssonDepartment of Clinical Sciences Lund, Division of Infection Medicine, Faculty of Medicine, Lund University, 221 84 Lund, Sweden.ORCID 0009-0009-0602-2183
Tobias SchmidtDepartment of Clinical Sciences Lund, Division of Pediatrics, Faculty of Medicine, Lund University, 221 84 Lund, Sweden.
Anna Söderlund-StrandDepartment of Laboratory Medicine, Clinical Microbiology, Skåne University Hospital Lund, Lund University, 221 85 Lund, Sweden.ORCID 0009-0001-8886-4385
Elizabeth ElderDepartment of Microbiology, National Veterinary Institute, 751 89 Uppsala, Sweden.ORCID 0000-0003-1615-2642
Sofia AppelbergDepartment of Microbiology, Public Health Agency of Sweden, 171 82 Stockholm, Sweden.ORCID 0000-0002-7381-3606
Maria ValsjöScantox A/S, 171 65 Stockholm, Sweden.
Olivia LarssonScantox A/S, 171 65 Stockholm, Sweden.
Vidar Wendel-HansenTanea Medical AB, 751 83 Uppsala, Sweden.ORCID 0009-0002-3179-1565
Mats OhlinDepartment of Immunotechnology, Faculty of Engineering, Lund University, 221 00 Lund, Sweden.ORCID 0000-0002-5105-1938
Wael BahnanDepartment of Clinical Sciences Lund, Division of Infection Medicine, Faculty of Medicine, Lund University, 221 84 Lund, Sweden.
Pontus NordenfeltDepartment of Clinical Sciences Lund, Division of Infection Medicine, Faculty of Medicine, Lund University, 221 84 Lund, Sweden.ORCID 0000-0002-9481-9951

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies play a central role in the immune defense against SARS-CoV-2. Emerging evidence has shown that nonneutralizing antibodies are important for immune defense through Fc-mediated effector functions. Antibody subclass is known to affect downstream Fc function. However, whether the antibody subclass plays a role in anti-SARS-CoV-2 immunity remains unclear. Here, we subclass-switched eight human IgG1 anti-spike monoclonal antibodies (mAbs) to the IgG3 subclass by exchanging their constant domains. The IgG3 mAbs exhibited altered avidities to the spike protein and more potent Fc-mediated phagocytosis and complement activation than their IgG1 counterparts. Moreover, combining mAbs into oligoclonal cocktails led to enhanced Fc- and complement receptor-mediated phagocytosis, superior to even the most potent single IgG3 mAb when compared at equivalent concentrations. Finally, in an in vivo model, we show that opsonic mAbs of both subclasses can be protective against a SARS-CoV-2 infection, despite the antibodies being nonneutralizing. Our results suggest that opsonic IgG3 oligoclonal cocktails are a promising idea to explore for therapy against SARS-CoV-2, its emerging variants, and potentially other viruses.

Indexed as

COVID-19Immunoglobulin GAntibodies, MonoclonalHumansOpsonizationPhagocytosisSARS-CoV-2Antibodies, MonoclonalImmunoglobulin GaffinityFc-mediated functionoligoclonalphagocytosissubclass

Identifiers

PMID37011197
PMCPMC10104557

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.