Evidence map›Paper›PMID 28952549›Full record

ArticleBioengineering (Basel, Switzerland)2017

In Vitro Evaluation of Glycoengineered RSV-F in the Human Artificial Lymph Node Reactor.

Lars Radke, Grit Sandig, Annika Lubitz, Ulrike Schließer, Hans Henning von Horsten, Veronique Blanchard, Karolin Keil, Volker Sandig, Christoph Giese, Michael Hummel and 2 more

Open access · goldAbstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

12 authors at 4 institutions in 1 country.

Lars RadkeMolecular Biotechnology and Functional Genomics, Technical University of Applied Sciences Wildau, Hochschulring 1, Wildau 15745, Germany. lars.radke@charite.de.
Grit SandigLaboratory of Biochemistry, Department of Life Sciences and Technology, Beuth University of Applied Sciences, Seestraße 64, Berlin 13347, Germany. Grit.Sandig@HTW-Berlin.de.
Annika LubitzProBioGen AG, Goethestraße 54, Berlin 13086, Germany. Annika.Lubitz@Probiogen.de.
Ulrike SchließerProBioGen AG, Goethestraße 54, Berlin 13086, Germany. Ulrike.Schliesser@Probiogen.de.
Hans Henning von HorstenDepartment of Life Science Engineering, HTW Berlin University of Applied Sciences, Wilhelminenhofstraße 75a, Berlin 12459, Germany. HansHenning.vonHorsten@htw-berlin.de.
Veronique BlanchardInstitute of Laboratory Medicine, Clinical Chemistry and Pathobiochemistry, Charité Medical University Berlin, Augustenburger Platz 1, Berlin 13353, Germany. veronique.blanchard@charite.de.
Karolin KeilMolecular Biotechnology and Functional Genomics, Technical University of Applied Sciences Wildau, Hochschulring 1, Wildau 15745, Germany. keil@th-wildau.de.
Volker SandigProBioGen AG, Goethestraße 54, Berlin 13086, Germany. Volker.Sandig@Probiogen.de.
Christoph GieseProBioGen AG, Goethestraße 54, Berlin 13086, Germany. Christoph.Giese@Probiogen.de.
Michael HummelInstitute of Pathology, Charitè-University Medicine Berlin, Augustenburger Platz 1, Berlin 13353, Germany. michael.hummel@charite.de.
Stephan HinderlichLaboratory of Biochemistry, Department of Life Sciences and Technology, Beuth University of Applied Sciences, Seestraße 64, Berlin 13347, Germany. hinderlich@beuth-hochschule.de.
Marcus FrohmeMolecular Biotechnology and Functional Genomics, Technical University of Applied Sciences Wildau, Hochschulring 1, Wildau 15745, Germany. mfrohme@th-wildau.de.
Technical University of Applied Sciences Wildau · DEBerliner Hochschule für Technik · DECharité - Universitätsmedizin Berlin · DEHTW Berlin - University of Applied Sciences · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subunit vaccines often require adjuvants to elicit sustained immune activity. Here, a method is described to evaluate the efficacy of single vaccine candidates in the preclinical stage based on cytokine and gene expression analysis. As a model, the recombinant human respiratory syncytial virus (RSV) fusion protein (RSV-F) was produced in CHO cells. For comparison, wild-type and glycoengineered, afucosylated RSV-F were established. Both glycoprotein vaccines were tested in a commercial Human Artificial Lymph Node in vitro model (HuALN

Indexed as

F-ProteinfucosylationGlycoengineeringNanoStringRSV

Identifiers

PMID28952549
PMCPMC5615316
OpenAlexW2746500672

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.