Evidence map›Paper›PMID 24533136›Full record

ArticlePloS one2014

Improved glucose metabolism in vitro and in vivo by an allosteric monoclonal antibody that increases insulin receptor binding affinity.

John A Corbin, Vinay Bhaskar, Ira D Goldfine, Daniel H Bedinger, Angela Lau, Kristen Michelson, Lisa M Gross, Betty A Maddux, Hua F Kuan, Catarina Tran and 15 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  8. Hypoglycemia After Gastric Bypass Surgery: Current Concepts and Controversies.The Journal of clinical endocrinology and metabolism · 2018
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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 2 institutions in 1 country.

John A CorbinDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Vinay BhaskarDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Ira D GoldfineDepartment of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Daniel H BedingerDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Angela LauDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Kristen MichelsonDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Lisa M GrossDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Betty A MadduxDepartment of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Hua F KuanDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Catarina TranDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Llewelyn LaoDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Masahisa HandaDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Susan R WatsonDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Ajay J NarasimhaDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Shirley ZhuDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Raphael LevyDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Lynn WebsterDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Sujeewa D WijesuriyaDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Naichi LiuDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Xiaorong WuDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
David Chemla-VogelDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Steve R LeeDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Steve WongDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Diane WilcockDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
Mark L WhiteDepartment of Preclinical Research, XOMA Corporation, Berkeley, California, United States of America.
XOMA (United States) · USUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously we reported studies of XMetA, an agonist antibody to the insulin receptor (INSR). We have now utilized phage display to identify XMetS, a novel monoclonal antibody to the INSR. Biophysical studies demonstrated that XMetS bound to the human and mouse INSR with picomolar affinity. Unlike monoclonal antibody XMetA, XMetS alone had little or no agonist effect on the INSR. However, XMetS was a strong positive allosteric modulator of the INSR that increased the binding affinity for insulin nearly 20-fold. XMetS potentiated insulin-stimulated INSR signaling ∼15-fold or greater including; autophosphorylation of the INSR, phosphorylation of Akt, a major enzyme in the metabolic pathway, and phosphorylation of Erk, a major enzyme in the growth pathway. The enhanced signaling effects of XMetS were more pronounced with Akt than with Erk. In cultured cells, XMetS also enhanced insulin-stimulated glucose transport. In contrast to its effects on the INSR, XMetS did not potentiate IGF-1 activation of the IGF-1 receptor. We studied the effect of XMetS treatment in two mouse models of insulin resistance and diabetes. The first was the diet induced obesity mouse, a hyperinsulinemic, insulin resistant animal, and the second was the multi-low dose streptozotocin/high-fat diet mouse, an insulinopenic, insulin resistant animal. In both models, XMetS normalized fasting blood glucose levels and glucose tolerance. In concert with its ability to potentiate insulin action at the INSR, XMetS reduced insulin and C-peptide levels in both mouse models. XMetS improved the response to exogenous insulin without causing hypoglycemia. These data indicate that an allosteric monoclonal antibody can be generated that markedly enhances the binding affinity of insulin to the INSR. These data also suggest that an INSR monoclonal antibody with these characteristics may have the potential to both improve glucose metabolism in insulinopenic type 2 diabetes mellitus and correct compensatory hyperinsulinism in insulin resistant conditions.

Indexed as

Allosteric SiteAnimalsAntibodies, MonoclonalAntigens, CDCell SeparationCHO CellsC-PeptideCricetinaeCricetulusDiabetes Mellitus, Type 2Flow CytometryGlucoseHumansHyperglycemiaHyperinsulinismInsulinAntibodies, MonoclonalAntigens, CDC-PeptideGlucoseINSR protein, humanInsulinPeptide LibraryReceptor, Insulin

Identifiers

PMID24533136
PMCPMC3922975
OpenAlexW2083342034

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.