Evidence map›Paper›PMID 27341129›Full record

ArticleOncotarget2016

Maturation of dendritic cells by pullulan promotes anti-cancer effect.

Wei Zhang, Xiaoqian Yu, Minseok Kwak, Li Xu, LiJun Zhang, Qing Yu, Jun-O Jin

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

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  11. The dynamic changes of CD3eParasitology research · 2017
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  12. Oncoimmunology
    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

7 authors at 4 institutions in 3 countries.

Wei ZhangShanghai Public Health Clinical Center, Shanghai Medical College, Fudan University, Shanghai, China.
Xiaoqian YuPeriodontal Department, Peking University School and Hospital of Stomatology, Beijing, China.
Minseok KwakDepartment of Chemistry, Pukyong National University, Busan, South Korea.
Li XuShanghai Public Health Clinical Center, Shanghai Medical College, Fudan University, Shanghai, China.
LiJun ZhangShanghai Public Health Clinical Center, Shanghai Medical College, Fudan University, Shanghai, China.
Qing YuDepartment of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
Jun-O JinShanghai Public Health Clinical Center, Shanghai Medical College, Fudan University, Shanghai, China.
Shanghai Public Health Clinical Center · CNHarvard University · USPeking University · CNPukyong National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies have demonstrated that pullulan, a polysaccharide purified from Aureobasidium pullulans, has immune-stimulatory effects on T and B cells. Moreover, pullulan has been used as a carrier in the delivery of the antigen (Ag) peptide to lymphoid tissues. However, the in vivo effect of pullulan on dendritic cells (DC) has not been well characterized. In this study, we assessed the effect of pullulan on DC activation and anti-cancer immunity. The results showed that the pullulan treatment up-regulated co-stimulatory molecule expression and enhanced pro-inflammatory cytokine production in bone marrow-derived DCs (BMDC) in vitro and in spleen DCs in vivo. Moreover, the combination of ovalbumin (OVA) and pullulan induced OVA antigen-specific T cell activations in vivo. In tumor-bearing mice, pullulan induced the maturation of DCs in spleen and tumor draining lymph node (drLN), and promoted the OVA-specific T cell activation and migration of the T cells into the tumor. In addition, the combination of OVA and pullulan inhibited B16-OVA tumor growth and liver metastasis. The combination of tyrosinase-related protein 2 (TRP2) peptide and pullulan treatment also suppressed B16 melanoma growth. Thus, the results demonstrated that pullulan enhanced DC maturation and function, and it acted as an adjuvant in promoting Ag-specific immune responses in mice. Thus, pullulan could be a new and useful adjuvant for use in therapeutic cancer vaccines.

Indexed as

AnimalsCell Line, TumorCells, CulturedCytokinesDendritic CellsDrug Therapy, CombinationGlucansMelanoma, ExperimentalMembrane ProteinsMice, Inbred C57BLMice, TransgenicOvalbuminPeptide FragmentsSurvival AnalysisT-LymphocytesTreatment OutcomeCytokinesGlucansMembrane ProteinsOvalbuminPeptide Fragmentspeptide SVYDFFVWLpullulanadjuvantanti-cancerdendritic cellimmunotherapypullulan

Identifiers

PMID27341129
PMCPMC5190125
OpenAlexW2465261539

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.