Evidence map›Paper›PMID 26647964›Full record

ArticleScientific reports2015

Suppression of established hepatocarcinoma in adjuvant only immunotherapy: alum triggers anti-tumor CD8+ T cell response.

Bo Wang, Xuanyi Wang, Yumei Wen, Jing Fu, Hongyang Wang, Zhangmei Ma, Yan Shi, Bin Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Alum: an old dog with new tricks.Emerging microbes & infections · 2016
    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 at 5 institutions in 2 countries.

Bo WangKey Laboratory of Molecular Medical Virology, MOE/MOH, Shanghai Medical College, Fudan University, Shanghai, China.
Xuanyi WangKey Laboratory of Molecular Medical Virology, MOE/MOH, Shanghai Medical College, Fudan University, Shanghai, China.
Yumei WenKey Laboratory of Molecular Medical Virology, MOE/MOH, Shanghai Medical College, Fudan University, Shanghai, China.
Jing FuInternational Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Institute/Hospital, and National Center for Liver Cancer, Shanghai, China.
Hongyang WangInternational Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Institute/Hospital, and National Center for Liver Cancer, Shanghai, China.
Zhangmei MaKey Laboratory of Molecular Medical Virology, MOE/MOH, Shanghai Medical College, Fudan University, Shanghai, China.
Yan ShiInstitute of Immunology, Department of Basic Medical Sciences, Center for Life Sciences, Tsinghua University, Beijing, China.
Bin WangKey Laboratory of Molecular Medical Virology, MOE/MOH, Shanghai Medical College, Fudan University, Shanghai, China.
Shanghai Medical College of Fudan University · CNEastern Hepatobiliary Surgery Hospital · CNFudan University · CNSecond Military Medical University · CNUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cell-based immunotherapy is a new weapon in our battle against malignancies in human. Recent trials in human and research work in model animals have shown various degrees of success, suggesting its great potential for clinical use. While protocols vary, a common scheme in this category of treatment involves activation of dendritic cells, with the purpose of increasing antigen presentation and cellular immunity. Therefore, proper use of immune adjuvant is a central subject of study. We report here an unexpected finding that injection of alum, the most widely used human adjuvant, into mice carrying H22 hepatocarcinoma resulted in a significant reduction of tumor growth with extended animal survival. This effect was associated with an increased specific CD8(+) T cell activation and an inflammatory environment, yet with minimal overt side effects. Our finding suggests that use of adjuvant alone in certain established tumors can invoke protective host immune activation against the same target, which may be of value in our development of new cancer immunotherapies.

Indexed as

Adjuvants, ImmunologicAlum CompoundsAnimalsCarcinoma, HepatocellularCD8-Positive T-LymphocytesCell Line, TumorChemokinesDisease Models, AnimalFemaleGene Expression RegulationHumansImmunomodulationLiver NeoplasmsLymphocyte ActivationMiceNeutrophil InfiltrationAdjuvants, ImmunologicAlum Compoundsaluminum sulfateChemokines

Identifiers

PMID26647964
PMCPMC4673419
OpenAlexW2291711054

What OpenQuestion holds

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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.