Evidence map›Paper›PMID 31949612›Full record

ArticleInternational journal of clinical and experimental pathology2018

TLR3 regulates PD-L1 expression in human cytomegalovirus infected glioblastoma.

Ziying Qin, Li Zhang, Yujiao Xu, Xianjuan Zhang, Xiaolu Fang, Dongmeng Qian, Xiaoke Liu, Ting Liu, Ling Li, Hong Yu and 1 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Does human cytomegalovirus provide a novel therapeutic target for patients with glioblastoma?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. 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

11 authors at 1 institution in 1 country.

Ziying QinDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Li ZhangDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Yujiao XuQingdao Hospital of Integrated Traditional and Western Medicine Qingdao, Shandong, PR China.
Xianjuan ZhangDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Xiaolu FangDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Dongmeng QianDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Xiaoke LiuDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Ting LiuDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Ling LiDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Hong YuDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Bin WangDepartment of Pathogenic Biology, Qingdao University Medical College Qingdao, Shandong, PR China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma, the most common primary brain tumor of adults, is characterized by poor survival rates. Programmed death ligand 1 (PD-L1, CD274) has been implicated in the immune escape of glioblastoma. The presence of human cytomegalovirus (HCMV) in glioblastoma multiforme (GBM) has sparked considerable interest and controversy. The exposure of toll-like receptor 3 (TLR3) to pathogens induces an antiviral state in cells or in animals. In the current study, the expression of PD-L1 and TLR3 in HCMV-infected glioma specimens was observed to be higher compared to the control. We therefore investigated if PD-L1 expression in glioblastoma is mediated by TLR3 triggering in HCMV infected glioblastoma. TLR3 siRNA transfections were utilized to identify the induction of PD-L1 via TLR3 triggering in HCMV infected cell lines. Also, IL-8 and TGF-β were detected by ELISA for the antitumor role of TLR3. Thus, we propose a novel immune treatment using a combination of PD-L1 blockade with TLR3 triggering against HCMV infected glioblastoma.

Indexed as

gliomaHCMVimmune treatmentPD-L1TLR3

Identifiers

PMID31949612
PMCPMC6963014
OpenAlexW3006139119

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.