Evidence map›Paper›PMID 23392215›Full record

ArticlemAbs

Rapid optimization and prototyping for therapeutic antibody-like molecules.

Lihui Xu, Neeraj Kohli, Rachel Rennard, Yang Jiao, Maja Razlog, Kathy Zhang, Jason Baum, Bryan Johnson, Jian Tang, Birgit Schoeberl and 3 more

Abstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Trial
  2. Toward Drug-Like Multispecific Antibodies by Design.International journal of molecular sciences · 2020
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Advances in Antibody Design.Annual review of biomedical engineering · 2015
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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

13 authors.

Lihui XuMerrimack Pharmaceuticals, Inc. Cambridge, MA, USA.
Neeraj Kohli
Rachel Rennard
Yang Jiao
Maja Razlog
Kathy Zhang
Jason Baum
Bryan Johnson
Jian Tang
Birgit Schoeberl
Jonathan Fitzgerald
Ulrik Nielsen
Alexey A Lugovskoy

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multispecific antibody-like molecules have the potential to advance the standard-of-care in many human diseases. The design of therapeutic molecules in this class, however, has proven to be difficult and, despite significant successes in preclinical research, only one trivalent antibody, catumaxomab, has demonstrated clinical utility. The challenge originates from the complexity of the design space where multiple parameters such as affinity, avidity, effector functions, and pharmaceutical properties need to be engineered in concurrent fashion to achieve the desired therapeutic efficacy. Here, we present a rapid prototyping approach that allows us to successfully optimize these parameters within one campaign cycle that includes modular design, yeast display of structure focused antibody libraries and high throughput biophysical profiling. We delineate this approach by presenting a design case study of MM-141, a tetravalent bispecific antibody targeting two compensatory signaling growth factor receptors: insulin-like growth factor 1 receptor (IGF-1R) and v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (ErbB3). A MM-141 proof-of-concept (POC) parent molecule did not meet initial design criteria due to modest bioactivity and poor stability properties. Using a combination of yeast display, structured-guided antibody design and library-scale thermal challenge assay, we discovered a diverse set of stable and active anti-IGF-1R and anti-ErbB3 single-chain variable fragments (scFvs). These optimized modules were reformatted to create a diverse set of full-length tetravalent bispecific antibodies. These re-engineered molecules achieved complete blockade of growth factor induced pro-survival signaling, were stable in serum, and had adequate activity and pharmaceutical properties for clinical development. We believe this approach can be readily applied to the optimization of other classes of bispecific or even multispecific antibody-like molecules.

Indexed as

Antibodies, BispecificDrug DesignSingle-Chain AntibodiesAnimalsAntibodies, MonoclonalCHO CellsCricetulusGene LibraryHEK293 CellsHigh-Throughput Screening AssaysHumansProtein EngineeringReceptor, ErbB-3Receptor, IGF Type 1Antibodies, BispecificAntibodies, MonoclonalERBB3 protein, humanReceptor, ErbB-3Receptor, IGF Type 1Single-Chain Antibodiesbispecific antibodiesErbB3high throughput screeningIGF-1RlibraryscFvyeast display

Identifiers

PMID23392215
PMCPMC3893234

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.