Evidence map›Paper›PMID 35396920›Full record

ArticleBiotechnology progress2022

Generation of a host cell line containing a MAR-rich landing pad for site-specific integration and expression of transgenes.

Claudia Oliviero, Steffen C Hinz, Jan P Bogen, Henri Kornmann, Björn Hock, Harald Kolmar, Gerrit Hagens

Open access · hybridAbstract read
In one paragraph

Article in Biotechnology progress, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Unique DNA impacts on transient Expi293Frontiers in bioengineering and biotechnology · 2026
    Article
  3. Article
  4. Article
  5. 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

7 authors at 3 institutions in 2 countries.

Claudia OlivieroInstitute of Life Technology, Haute Ecole d'Ingénierie HES-SO Valais Wallis, Sion, Switzerland.
Steffen C HinzInstitute of Life Technology, Haute Ecole d'Ingénierie HES-SO Valais Wallis, Sion, Switzerland.
Jan P BogenInstitute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, Darmstadt, Germany.
Henri KornmannFerring Biologics Innovation Center, Epalinges, Switzerland.
Björn HockFerring Biologics Innovation Center, Epalinges, Switzerland.
Harald KolmarInstitute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, Darmstadt, Germany.
Gerrit HagensInstitute of Life Technology, Haute Ecole d'Ingénierie HES-SO Valais Wallis, Sion, Switzerland.ORCID 0000-0001-6240-6071
HES-SO Valais-Wallis · CHFerring Pharmaceuticals (Switzerland) · CHTechnische Universität Darmstadt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, targeted gene integration (TI) has been introduced as a strategy for the generation of recombinant mammalian cell lines for the production of biotherapeutics. Besides reducing the immense heterogeneity within a pool of recombinant transfectants, TI also aims at shortening the duration of the current cell line development process. Here we describe the generation of a host cell line carrying Matrix-Attachment Region (MAR)-rich landing pads (LPs), which allow for the simultaneous and site-specific integration of multiple genes of interest (GOIs). We show that several copies of each chicken lysozyme 5'MAR-based LP containing either BxB1 wild type or mutated recombination sites, integrated at one random chromosomal locus of the host cell genome. We further demonstrate that these LP-containing host cell lines can be used for the site-specific integration of several GOIs and thus, generation of transgene-expressing stable recombinant clones. Transgene expression was shown by site-specific integration of heavy and light chain genes coding for a monospecific antibody (msAb) as well as for a bi-specific antibody (bsAb). The genetic stability of the herein described LP-based recombinant clones expressing msAb or bsAb was demonstrated by cultivating the recombinant clones and measuring antibody titers over 85 generations. We conclude that the host cell containing multiple copies of MAR-rich landing pads can be successfully used for stable expression of one or several GOIs.

Indexed as

GenomeAnimalsCHO CellsCricetinaeCricetulusRecombinant ProteinsTransgenesRecombinant ProteinsantibodyCHO cellsprotein expressionrecombinant proteinsite-specific integration

Identifiers

PMID35396920
PMCPMC9539524
OpenAlexW4223453082

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.