Evidence map›Paper›PMID 32116691›Full record

ArticleFrontiers in pharmacology2020

A Novel C Type CpG Oligodeoxynucleotide Exhibits Immunostimulatory Activity

Tete Li, Jing Wu, Shan Zhu, Guoxia Zang, Shuang Li, Xinping Lv, Wenjun Yue, Yuan Qiao, Jiuwei Cui, Yan Shao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. 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
0.9field-weighted citation impact, top 28% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. CpG-Based Nanovaccines for Cancer Immunotherapy.International journal of nanomedicine · 2021
    Review
  7. Review
  8. Review
  9. 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

13 authors at 2 institutions in 1 country.

Tete LiInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Jing WuInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Shan ZhuInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Guoxia ZangInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Shuang LiInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Xinping LvInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Wenjun YueInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Yuan QiaoInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Jiuwei CuiCancer Center, The First Hospital of Jilin University, Changchun, China.
Yan ShaoChangchun Huapu Biotechnology Co., Ltd., Changchun, China.
Jun ZhangChangchun Huapu Biotechnology Co., Ltd., Changchun, China.
Yong-Jun LiuInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
Jingtao ChenInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun, China.
First Hospital of Jilin University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundC type CpG oligodeoxynucleotides (CpG-C ODNs), possessing the features of both A type and B type CpG ODNs, exert a variety of immunostimulatory activities and have been demonstrated as an effective antitumor immunotherapy. Based on the structural characteristics, we designed 20 potential ODNs with the aim of synthesizing an optimal, novel CpG-C ODN specific to human and murine Toll-like receptor 9 (TLR9). We also sought to investigate the

methodsTwenty potential CpG-C ODNs were screened for their ability to secrete interferon (IFN)-α, and interleukin (IL)-6 and tumor necrosis factor (TNF)-α production for the three most promising sequences were assayed in human peripheral blood mononuclear cells (PBMCs) by enzyme-linked immunosorbent assay (ELISA) or cytometric bead array assay. The functions of human and mouse B cells, and cytokine production in mice induced by the most promising sequence, HP06T07, were determined by flow cytometry and ELISA. Growth and morphology of tumor tissues in

resultsAmong the 20 designed ODNs, HP06T07 significantly induced IFN-α, IL-6, and TNF-α secretion, and promoted B-cell activation and proliferation in a dose-dependent manner in human PBMCs and mouse splenocytes

conclusionsHP06T07, a novel CpG-C ODN, shows potent immunostimulatory activity

Indexed as

antitumor immunotherapyB cellscytosine-phosphate-guanosine dinucleotide-containing oligodeoxynucleotidesplasmacytoid dendritic cellsToll-like receptor 9

Identifiers

PMID32116691
PMCPMC7015978
OpenAlexW3004732178

What OpenQuestion holds

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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.