Evidence map›Paper›PMID 33172091›Full record

ArticleAntibodies (Basel, Switzerland)2020

Bringing the Heavy Chain to Light: Creating a Symmetric, Bivalent IgG-Like Bispecific.

Anusuya Ramasubramanian, Rachel Tennyson, Maureen Magnay, Sagar Kathuria, Tara Travaline, Annu Jain, Dana M Lord, Megan Salemi, Caitlin Sullivan, Tristan Magnay and 8 more

Abstract read
In one paragraph

Article in Antibodies (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

18 authors.

Anusuya RamasubramanianBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.ORCID 0000-0001-7178-7734
Rachel TennysonBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Maureen MagnayBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.ORCID 0000-0002-0865-9710
Sagar KathuriaBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Tara TravalineBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Annu JainBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Dana M LordBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.ORCID 0000-0001-9060-1210
Megan SalemiBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Caitlin SullivanBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Tristan MagnayBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.ORCID 0000-0001-7649-6960
Jiali HuBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Eva Bric-FurlongBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Pierrick RivalBiologics Research, Sanofi R&D, 13 Quai Jules Guesde, 94403 Vitry-sur-Seine, France.
Yanfeng ZhouBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Dietmar HoffmannBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
William BrondykBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.
Katarina RadoševićBiologics Research, Sanofi R&D, 13 Quai Jules Guesde, 94403 Vitry-sur-Seine, France.
Partha S ChowdhuryBiologics Research, Sanofi R&D, 49 New York Avenue, Framingham, MA 01701, USA.ORCID 0000-0003-0990-4658

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bispecific molecules are biologically significant, yet their complex structures pose important manufacturing and pharmacokinetic challenges. Nevertheless, owing to similarities with monoclonal antibodies (mAbs), IgG-like bispecifics conceptually align well with conventional expression and manufacturing platforms and often exhibit potentially favorable drug metabolism and pharmacokinetic (DMPK) properties. However, IgG-like bispecifics do not possess target bivalency and current designs often require tedious engineering and purification to ensure appropriate chain pairing. Here, we present a near-native IgG antibody format, the 2xVH, which can create bivalency for each target or epitope and requires no engineering for cognate chain pairing. In this modality, two different variable heavy (VH) domains with distinct binding specificities are grafted onto the first constant heavy (CH1) and constant light (CL) domains, conferring the molecule with dual specificity. To determine the versatility of this format, we characterized the expression, binding, and stability of several previously identified soluble human VH domains. By grafting these domains onto an IgG scaffold, we generated several prototype 2xVH IgG and Fab molecules that display similar properties to mAbs. These molecules avoided the post-expression purification necessary for engineered bispecifics while maintaining a capacity for simultaneous dual binding. Hence, the 2xVH format represents a bivalent, bispecific design that addresses limitations of manufacturing IgG-like bispecifics while promoting biologically-relevant dual target engagement.

Indexed as

2xVHbivalent bispecific moleculeconcomittant bindingIgG-like bispecificssoluble VHsymmetrical bispecific

Identifiers

PMID33172091
PMCPMC7709125

What OpenQuestion holds

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Registered trials

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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.