Evidence map›Paper›PMID 31727737›Full record

ArticleThe Journal of biological chemistry2019

The impact of thioredoxin reduction of allosteric disulfide bonds on the therapeutic potential of monoclonal antibodies.

Shalom A Gurjar, Jun X Wheeler, Meenu Wadhwa, Robin Thorpe, Ian Kimber, Jeremy P Derrick, Rebecca J Dearman, Clive Metcalfe

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 16 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

8 authors at 2 institutions in 1 country.

Shalom A GurjarDivision of Biotherapeutics, The National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Potters Bar, Hertfordshire EN6 3QG, United Kingdom.
Jun X WheelerDivision of Technology Development and Infrastructure, National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Potters Bar, Hertfordshire EN6 3QG, United Kingdom.
Meenu WadhwaDivision of Biotherapeutics, The National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Potters Bar, Hertfordshire EN6 3QG, United Kingdom.
Robin ThorpeDivision of Biotherapeutics, The National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Potters Bar, Hertfordshire EN6 3QG, United Kingdom.
Ian KimberLydia Becker Institute of Immunology and Inflammation, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester M13 9PT, United Kingdom.
Jeremy P DerrickLydia Becker Institute of Immunology and Inflammation, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester M13 9PT, United Kingdom.
Rebecca J DearmanLydia Becker Institute of Immunology and Inflammation, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester M13 9PT, United Kingdom.
Clive MetcalfeDivision of Biotherapeutics, The National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Potters Bar, Hertfordshire EN6 3QG, United Kingdom clive.metcalfe@nibsc.org.ORCID 0000-0002-7856-8574
National Institute for Biological Standards and Control · GBManchester Academic Health Science Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic mAbs are used to manage a wide range of cancers and autoimmune disorders. However, mAb-based treatments are not always successful, highlighting the need for a better understanding of the factors influencing mAb efficacy. Increased levels of oxidative stress associated with several diseases are counteracted by the activities of various oxidoreductase enzymes, such as thioredoxin (Trx), which also reduces allosteric disulfide bonds in proteins, including mAbs. Here, using an array of

Indexed as

Allosteric SiteAntibodies, MonoclonalAntibody-Dependent Cell CytotoxicityAntigensAntineoplastic Agents, ImmunologicalB-LymphocytesCell LineCell MembraneCell ProliferationComplement System ProteinsDisulfidesErb-b2 Receptor Tyrosine KinasesHumansImmunoglobulin Fc FragmentsImmunoglobulin GKineticsAntibodies, MonoclonalAntigensAntineoplastic Agents, ImmunologicalComplement System ProteinsDisulfidesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesImmunoglobulin Fc FragmentsImmunoglobulin GOxygenProtein-Tyrosine KinasesThioredoxinsTrastuzumaballosteric regulationantibody-dependent cellular cytotoxicity (ADCC)biotherapeuticcomplement-dependent cytotoxicity (CDC)disulfidedisulfide bondfunctional effectsmonoclonal antibodyredox regulationsafety and efficacythioredoxin (Trx)

Identifiers

PMID31727737
PMCPMC6926469
OpenAlexW2986616908

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.