Evidence map›Paper›PMID 32021567›Full record

ArticleJournal of inflammation (London, England)2020

Dendritic cells transduced with glioma-expressed antigen 2 recombinant adenovirus induces specific cytotoxic lymphocyte response and anti-tumor effect in mice.

Gaohai Shao, Changlong Zhou, Kunlong Ma, Wang Zhao, Guibo Feng, Qijiang Xiong, Ling Yang, Zhao Yang

Abstract read
In one paragraph

Article in Journal of inflammation (London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

8 authors.

Gaohai Shao1Department of orthopedics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.
Changlong Zhou2Department of Neurology, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.
Kunlong Ma1Department of orthopedics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.
Wang Zhao2Department of Neurology, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.
Guibo Feng2Department of Neurology, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.
Qijiang Xiong2Department of Neurology, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.
Ling Yang2Department of Neurology, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.
Zhao Yang2Department of Neurology, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160 China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGlioma is an aggressive common cancer with high mortality worldwide. Up to date, the effective medical therapeutical strategy is limited. Numerous previous studies have indicated that glioma-expressed antigen 2 (GLEA2) might be an attractive prognostic glioma biomarker.

methodsIn this experiment, dendritic cells (DCs) transduced with GLEA2 recombinant adenovirus were utilized to generate cytotoxic lymphocytes (CTLs) in vitro. Additionally, trimera mice were immunized with the transduced DCs to generate CTLs in vivo.

resultsThe data demonstrated that GLEA2 transduced DCs could effectively generate specific CTL response against glioma without lysing autologous lymphocytes. Moreover, GLEA2 transduced DCs significantly attenuated the tumor growth and prolonged the life span of tumor bearing mice.

conclusionsThese findings suggested that DCs transduced with GLEA2 recombinant adenovirus could generate effective CTL mediated anti-tumor response, and might represent insight in glioma therapy.

Indexed as

Anti-tumorCTLDendritic cellsGLEA2

Identifiers

PMID32021567
PMCPMC6995099

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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.