Evidence map›Paper›PMID 34869052›Full record

ArticleFrontiers in cellular and infection microbiology2021

Shelf-Life Extension of Fc-Fused Single Chain Fragment Variable Antibodies by Lyophilization.

Kai-Thomas Schneider, Toni Kirmann, Esther Veronika Wenzel, Jan-Hendrik Grosch, Saskia Polten, Doris Meier, Marlies Becker, Paul Matejtschuk, Michael Hust, Giulio Russo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. A single dose of a vectorized mAb targeting TDP-43 potently inhibits the neuropathology in a model of ALS/FTD.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Antibody Batch Cloning.Methods in molecular biology (Clifton, N.J.) · 2023
    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

11 authors at 3 institutions in 2 countries.

Kai-Thomas SchneiderDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Toni KirmannDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Esther Veronika WenzelDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Jan-Hendrik GroschInstitute of Biochemical Engineering, Technische Universität Braunschweig, Braunschweig, Germany.
Saskia PoltenDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Doris MeierDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Marlies BeckerDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Paul MatejtschukStandardisation Science, National Institute for Biological Standards & Control (NIBSC), Hertfordshire, United Kingdom.
Michael HustDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Giulio RussoDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Stefan DübelDepartment of Biotechnology, Technische Universität Braunschweig, Braunschweig, Germany.
Technische Universität Braunschweig · DEAmedes Genetics (Germany) · DENational Institute for Biological Standards and Control · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generation of sequence defined antibodies from universal libraries by phage display has been established over the past three decades as a robust method to cope with the increasing market demand in therapy, diagnostics and research. For applications requiring the bivalent antigen binding and an Fc part for detection, phage display generated single chain Fv (scFv) antibody fragments can rapidly be genetically fused to the Fc moiety of an IgG for the production in eukaryotic cells of antibodies with IgG-like properties. In contrast to conversion of scFv into IgG format, the conversion to scFv-Fc requires only a single cloning step, and provides significantly higher yields in transient cell culture production than IgG. ScFv-Fcs can be effective as neutralizing antibodies

Indexed as

Single-Chain AntibodiesAntibodies, NeutralizingCell Surface Display TechniquesFreeze DryingLife ExpectancyAntibodies, NeutralizingSingle-Chain Antibodiesantibody formattingantibody stabilityfreeze-dryingIgGlyophilizationphage displayrecombinant antibodyscFv-Fc

Identifiers

PMID34869052
PMCPMC8634725
OpenAlexW3211664192

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.