Evidence map›Paper›PMID 28970485›Full record

ArticleScientific reports2017

The hUC-MSCs cell line CCRC-1 represents a novel, safe and high-yielding HDCs for the production of human viral vaccines.

Ping Chen, Ke-Hua Zhang, Tao Na, Lin Wang, Wei-Dong Yin, Bao-Zhu Yuan, Jun-Zhi Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
2.0field-weighted citation impact, top 13% 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, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. 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

7 authors at 2 institutions in 1 country.

Ping ChenCell Collection and Research Center, National Institutes for Food and Drug Control, Beijing, 100050, PR China.
Ke-Hua ZhangCell Collection and Research Center, National Institutes for Food and Drug Control, Beijing, 100050, PR China.
Tao NaCell Collection and Research Center, National Institutes for Food and Drug Control, Beijing, 100050, PR China.
Lin WangSino Vac Biotech, Beijing, 100085, PR China.
Wei-Dong YinSino Vac Biotech, Beijing, 100085, PR China.
Bao-Zhu YuanCell Collection and Research Center, National Institutes for Food and Drug Control, Beijing, 100050, PR China. ybao4356@gmail.com.
Jun-Zhi WangCell Collection and Research Center, National Institutes for Food and Drug Control, Beijing, 100050, PR China. wangjz@nifdc.org.cn.
National Institutes for Food and Drug Control · CNSinovac Biotech · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MRC-5 represents the most frequent human diploid cells (HDCs)-type cell substrate in the production of human viral vaccines. However, early-passage MRC-5 is diminishing and, due to both technical and ethical issues, it is extremely difficult to derive novel HDCs from fetal lung tissues, which are the common sources of HDCs. Our previous studies suggested that human umbilical cord may represent an alternative but convenient source of new HDCs. Here, we established a three-tiered cell banking system of a hUC-MSC line, designated previously as Cell Collection and Research Center-1 (CCRC-1). The full characterization indicated that the banked CCRC-1 cells were free from adventitious agents and remained non-tumorigenic. The CCRC-1 cells sustained its rapid proliferation even at passage 30 and were susceptible to the infection of a wide spectrum of viruses. Interestingly, the CCRC-1 cells showed much higher production of EV71 or Rubella viruses than MRC-5 and Vero cells when growing in serum-free medium. More importantly, the EV71 vaccine produced from CCRC-1 cells induced immunogenicity while eliciting no detectable toxicities in the tested mice. Collectively, these studies further supported that CCRC-1, and likely other hUC-MSCs as well, may serve as novel, safe and high-yielding HDCs for the production of human viral vaccines.

Indexed as

VaccinationAnimalsBiological Specimen BanksCell LineCell ProliferationChlorocebus aethiopsCulture Media, Serum-FreeDiploidyEnterovirus A, HumanEnterovirus InfectionsFemaleFetal BloodHumansImmunogenicity, VaccineMesenchymal Stem CellsMiceCulture Media, Serum-FreeViral Vaccines

Identifiers

PMID28970485
PMCPMC5624879
OpenAlexW2758048118

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.