Evidence map›Paper›PMID 31544872›Full record

ArticleAntibodies (Basel, Switzerland)2018

Allosteric Effects between the Antibody Constant and Variable Regions: A Study of IgA Fc Mutations on Antigen Binding.

Chinh Tran-To Su, Wai-Heng Lua, Wei-Li Ling, Samuel Ken-En Gan

Open access · goldAbstract read
In one paragraph

Article in Antibodies (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.7field-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

32 citing papers in PubMed, 51 citations in OpenAlex.

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  14. Science immunology · 2021
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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

4 authors at 1 institution in 1 country.

Chinh Tran-To SuBioinformatics Institute, Agency for Science, Technology and Research (A*STAR), Singapore 138671, Singapore. chinhsutranto@bii.a-star.edu.sg.
Wai-Heng LuaBioinformatics Institute, Agency for Science, Technology and Research (A*STAR), Singapore 138671, Singapore. luawh@bii.a-star.edu.sg.
Wei-Li LingBioinformatics Institute, Agency for Science, Technology and Research (A*STAR), Singapore 138671, Singapore. lingwl@bii.a-star.edu.sg.
Samuel Ken-En GanBioinformatics Institute, Agency for Science, Technology and Research (A*STAR), Singapore 138671, Singapore. samuelg@bii.a-star.edu.sg.ORCID 0000-0001-9936-5090
Agency for Science, Technology and Research · SG

Funding

Agency for Science, Technology and Research BioMedical Research Council Young Investigator Grant (BMRC YIG 1510651021)Agency for Science, Technology and Research Joint Council Office (JCO1334i00050)
6 · The paper itself

Abstract

Therapeutic antibodies have shifted the paradigm of disease treatments from small molecules to biologics, especially in cancer therapy. Despite the increasing number of antibody candidates, much remains unknown about the antibody and how its various regions interact. Recent findings showed that the antibody constant region can govern localization effects that are useful in reducing side effects due to systemic circulation by the commonly used IgG isotypes. Given their localized mucosal effects, IgA antibodies are increasingly promising therapeutic biologics. While the antibody Fc effector cell activity has been a focus point, recent research showed that the Fc could also influence antigen binding, challenging the conventional idea of region-specific antibody functions. To investigate this, we analysed the IgA antibody constant region and its distal effects on the antigen binding regions using recombinant Pertuzumab IgA1 and IgA2 variants. We found that mutations in the C-region reduced Her2 binding experimentally, and computational structural analysis showed that allosteric communications were highly dependent on the antibody hinge, providing strong evidence that we should consider antibodies as whole proteins rather than a sum of functional regions.

Indexed as

allostericantibodybiologicsconstant regionisotype IgAPertuzumabvariable region

Identifiers

PMID31544872
PMCPMC6698812
OpenAlexW2805620739

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.