Evidence map›Paper›PMID 27416017›Full record

ReviewmAbs2016

Phage display-derived human antibodies in clinical development and therapy.

André Frenzel, Thomas Schirrmann, Michael Hust

Registry-linked trialAbstract readReview
In one paragraph

Review in mAbs, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05889338 (Impact of Adalimumab Therapy on Quality of Life of Patients With Severe Psoriasis), which is not on this map. Cited by 178 papers.

0numbers the graph read from it
0cells of the map it votes in
178citing 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.

NCT05889338 naunknown statusnot on this mapstarted 2023, after this paper: background citation

Impact of Adalimumab Therapy on Quality of Life of Patients With Severe Psoriasis

TypeinterventionalSponsorSohag UniversityRan2023 to 2024Enrolled140ConditionsPsoriasiArmsadalimumab and methotrexate
3 · Its place in the literature

Who cites it

178 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Technologies for Monoclonal Antibody Discovery and Development.International journal of molecular sciences · 2025
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Protein CREATE enables closed-loop design ofbioRxiv : the preprint server for biology · 2025
    Article
  20. Review

118 more citing papers are in PubMed but not listed here.

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

3 authors.

André Frenzela YUMAB GmbH , Rebenring , Braunschweig.
Thomas Schirrmanna YUMAB GmbH , Rebenring , Braunschweig.
Michael Hustb Technische Universität Braunschweig, Institut für Biochemie, Biotechnologie und Bioinformatik, Abteilung Biotechnologie , Braunschweig , Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the last 3 decades, monoclonal antibodies have become the most important class of therapeutic biologicals on the market. Development of therapeutic antibodies was accelerated by recombinant DNA technologies, which allowed the humanization of murine monoclonal antibodies to make them more similar to those of the human body and suitable for a broad range of chronic diseases like cancer and autoimmune diseases. In the early 1990s in vitro antibody selection technologies were developed that enabled the discovery of "fully" human antibodies with potentially superior clinical efficacy and lowest immunogenicity. Antibody phage display is the first and most widely used of the in vitro selection technologies. It has proven to be a robust, versatile platform technology for the discovery of human antibodies and a powerful engineering tool to improve antibody properties. As of the beginning of 2016, 6 human antibodies discovered or further developed by phage display were approved for therapy. In 2002, adalimumab (Humira®) became the first phage display-derived antibody granted a marketing approval. Humira® was also the first approved human antibody, and it is currently the best-selling antibody drug on the market. Numerous phage display-derived antibodies are currently under advanced clinical investigation, and, despite the availability of other technologies such as human antibody-producing transgenic mice, phage display has not lost its importance for the discovery and engineering of therapeutic antibodies. Here, we provide a comprehensive overview about phage display-derived antibodies that are approved for therapy or in clinical development. A selection of these antibodies is described in more detail to demonstrate different aspects of the phage display technology and its development over the last 25 years.

Indexed as

Antibodies, MonoclonalCell Surface Display TechniquesDrug DiscoveryHumansAntibodies, MonoclonalAntibody engineeringbiologicsclinical developmentFabhuman antibodiesphage displayrecombinant antibodiesscFvtherapeutic antibodies

Identifiers

PMID27416017
PMCPMC5058633

What OpenQuestion holds

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Registered trials

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.