Evidence map›Paper›PMID 29553863›Full record

ArticlemAbs2018

Reformatting palivizumab and motavizumab from IgG to human IgA impairs their efficacy against RSV infection in vitro and in vivo.

Shamir R Jacobino, Maaike Nederend, J Frederiek Reijneveld, Daan Augustijn, J H Marco Jansen, Jan Meeldijk, Karli R Reiding, Manfred Wuhrer, Frank E J Coenjaerts, C Erik Hack and 2 more

Open access · goldAbstract read
In one paragraph

Article in mAbs, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 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

12 authors at 2 institutions in 1 country.

Shamir R Jacobinoa Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
Maaike Nederenda Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
J Frederiek Reijnevelda Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
Daan Augustijna Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
J H Marco Jansena Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
Jan Meeldijka Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
Karli R Reidingb Center for Proteomics and Metabolomics , Leiden University Medical Center , Leiden , The Netherlands.
Manfred Wuhrerb Center for Proteomics and Metabolomics , Leiden University Medical Center , Leiden , The Netherlands.
Frank E J Coenjaertsc Department of Medical Microbiology , UMC Utrecht , Utrecht , The Netherlands.ORCID 0000-0001-6054-3590
C Erik Hacka Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
Louis J Bonta Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.
Jeanette H W Leusena Laboratory of Translational Immunology , UMC Utrecht , Utrecht , The Netherlands.ORCID 0000-0003-4982-6914
University Medical Center Utrecht · NLLeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) infection is a leading cause of hospitalization and mortality in young children. Protective therapy options are limited. Currently, palivizumab, a monoclonal IgG1 antibody, is the only licensed drug for RSV prophylaxis, although other IgG antibody candidates are being evaluated. However, at the respiratory mucosa, IgA antibodies are most abundant and act as the first line of defense against invading pathogens. Therefore, it would be logical to explore the potential of recombinant human IgA antibodies to protect against viral respiratory infection, but very little research on the topic has been published. Moreover, it is unknown whether human antibodies of the IgA isotype are better suited than those of the IgG isotype as antiviral drugs to combat respiratory infections. To address this, we generated various human IgA antibody formats of palivizumab and motavizumab, two well-characterized human IgG1 anti-RSV antibodies. We evaluated their efficacy to prevent RSV infection in vitro and in vivo and found similar, but somewhat decreased efficacy for different IgA subclasses and formats. Thus, reformatting palivizumab or motavizumab into IgA reduces the antiviral potency of either antibody. Moreover, our results indicate that the efficacy of intranasal IgA prophylaxis against RSV infection in human FcαRI transgenic mice is independent of Fc receptor expression.

Indexed as

Antibodies, Monoclonal, HumanizedAntibodies, ViralImmunoglobulin AImmunoglobulin GPalivizumabRespiratory Syncytial Virus InfectionsAnimalsCell LineHumansMiceMice, Inbred BALB CMice, TransgenicProtein EngineeringRespiratory Syncytial VirusesAntibodies, Monoclonal, HumanizedAntibodies, ViralImmunoglobulin AImmunoglobulin GmotavizumabPalivizumabantibody glycosylationdIgAFc receptorfusion proteinIgGmIgAmotavizumabneutralizing antibodiespalivizumabRSVsIgA

Identifiers

PMID29553863
PMCPMC5939987
OpenAlexW2790790081

What OpenQuestion holds

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LicenceCC BY-NC
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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.