Evidence map›Paper›PMID 31383491›Full record

ArticleVaccine2019

Recombinant hemagglutinin produced from Chinese Hamster Ovary (CHO) stable cell clones and a PELC/CpG combination adjuvant for H7N9 subunit vaccine development.

Ting-Hsuan Chen, Wen-Chun Liu, I-Chen Chen, Chia-Chyi Liu, Ming-Hsi Huang, Jia-Tsrong Jan, Suh-Chin Wu

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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 1 country.

Ting-Hsuan ChenInstitute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan.
Wen-Chun LiuInstitute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan.
I-Chen ChenInstitute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan.
Chia-Chyi LiuNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan.
Ming-Hsi HuangNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan.
Jia-Tsrong JanGenomics Research Center, Academia Sinica, Taipei 11529, Taiwan.
Suh-Chin WuInstitute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan; Department of Medical Science, National Tsing Hua University, Hsinchu 30013, Taiwan. Electronic address: scwu@mx.nthu.edu.tw.
National Tsing Hua University · TWNational Health Research Institutes · TWGenomics Research Center, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The novel H7N9 avian influenza A virus has caused human infections in China since 2013; some isolates from the fifth wave of infections have emerged as highly pathogenic avian influenza viruses. Recombinant hemagglutinin proteins of H7N9 viruses can be rapidly and efficiently produced with low-level biocontainment facilities. In this study, recombinant H7 antigen was obtained from engineered stable clones of Chinese Hamster Ovary (CHO) cells for subsequent large-scale production. The stable CHO cell clones were also adapted to grow in serum-free suspension cultures. To improve the immunogenicity of the recombinant H7 antigens, we evaluated the use of a novel combination adjuvant of PELC and CpG (PELC/CpG) to augment the anti-H7N9 immune responses in mice. We compared the effects with other adjuvants such as alum, AddaVax (MF59-like), and several Toll-like receptor ligands such as R848, CpG, and poly (I:C). With the PELC/CpG combination adjuvant, CHO cell-expressed rH7 antigens containing terminally sialylated complex type N-glycans were able to induce high titers of neutralizing antibodies in sera and conferred protection following live virus challenges. These data indicate that the CHO cell-expressed recombinant H7 antigens and a PELC/CpG combination adjuvant can be used for H7N9 subunit vaccine development.

Indexed as

Adjuvants, ImmunologicAlum CompoundsAnimalsAntibodies, NeutralizingAntibodies, ViralCell LineCHO CellsCpG IslandsCricetulusFemaleHemagglutination Inhibition TestsHemagglutinin Glycoproteins, Influenza VirusHemagglutininsInfluenza A Virus, H7N9 SubtypeInfluenza VaccinesMiceAddavaxAdjuvants, ImmunologicAlum Compoundsaluminum sulfateAntibodies, NeutralizingAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusHemagglutininsInfluenza VaccinesPolysorbatesRecombinant ProteinsSqualeneVaccines, SubunitCHO cellsH7N9 vaccineHemagglutininPELC/CpG adjuvant

Identifiers

PMID31383491
PMCPMC7115541
OpenAlexW2965603371

What OpenQuestion holds

Textmetadata
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.