Evidence map›Paper›PMID 37088780›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Biomaterials Facilitating Dendritic Cell-Mediated Cancer Immunotherapy.

Heng Dong, Qiang Li, Yu Zhang, Meng Ding, Zhaogang Teng, Yongbin Mou

Open access · goldAbstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
12.0field-weighted citation impact, top 1% 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

34 citing papers in PubMed, 73 citations in OpenAlex.

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  16. Ferrum@albumin assembled nanoclusters inhibit NF-Acta pharmaceutica Sinica. B · 2025
    Article
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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

6 authors at 2 institutions in 1 country.

Heng DongNanjing Stomatological Hospital, Affiliated Hospital of Medical School, Nanjing University, 30 Zhongyang Road, Nanjing, Jiangsu, 210008, P. R. China.ORCID 0000-0002-2537-7950
Qiang LiNanjing Stomatological Hospital, Affiliated Hospital of Medical School, Nanjing University, 30 Zhongyang Road, Nanjing, Jiangsu, 210008, P. R. China.ORCID 0000-0002-9086-8502
Yu ZhangNanjing Stomatological Hospital, Affiliated Hospital of Medical School, Nanjing University, 30 Zhongyang Road, Nanjing, Jiangsu, 210008, P. R. China.ORCID 0000-0002-8681-3867
Meng DingNanjing Stomatological Hospital, Affiliated Hospital of Medical School, Nanjing University, 30 Zhongyang Road, Nanjing, Jiangsu, 210008, P. R. China.
Zhaogang TengKey Laboratory for Organic Electronics and Information Displays, Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials, Jiangsu National Synergetic Innovation Centre for Advanced Materials, Nanjing University of Posts and Telecommunications, 9 Wenyuan Road, Nanjing, Jiangsu, 210023, P. R. China.ORCID 0000-0001-8792-764X
Yongbin MouNanjing Stomatological Hospital, Affiliated Hospital of Medical School, Nanjing University, 30 Zhongyang Road, Nanjing, Jiangsu, 210008, P. R. China.ORCID 0000-0003-0964-2862
Nanjing Medical University · CNNanjing University of Posts and Telecommunications · CN

Funding

"3456" Cultivation Program for Junior Talents of Nanjing Stomatological Hospital, Medical School of Nanjing University 0222R212Jiangsu Provincial Key Research and Development Program BE2020629Nanjing Medical Science and Technique Development Foundation YKK19094National Natural Sciences Foundation of China 22275099National Natural Sciences Foundation of China 81571800National Natural Sciences Foundation of China 81971675Project of State Key Laboratory of Organic Electronics and Information Displays, the Nanjing University of Posts & Telecommunications GDX2022010014
6 · The paper itself

Abstract

Dendritic cell (DC)-based cancer immunotherapy has exhibited remarkable clinical prospects because DCs play a central role in initiating and regulating adaptive immune responses. However, the application of traditional DC-mediated immunotherapy is limited due to insufficient antigen delivery, inadequate antigen presentation, and high levels of immunosuppression. To address these challenges, engineered biomaterials have been exploited to enhance DC-mediated immunotherapeutic effects. In this review, vital principal components that can enhance DC-mediated immunotherapeutic effects are first introduced. The parameters considered in the rational design of biomaterials, including targeting modifications, size, shape, surface, and mechanical properties, which can affect biomaterial optimization of DC functions, are further summarized. Moreover, recent applications of various engineered biomaterials in the field of DC-mediated immunotherapy are reviewed, including those serve as immune component delivery platforms, remodel the tumor microenvironment, and synergistically enhance the effects of other antitumor therapies. Overall, the present review comprehensively and systematically summarizes biomaterials related to the promotion of DC functions; and specifically focuses on the recent advances in biomaterial designs for DC activation to eradicate tumors. The challenges and opportunities of treatment strategies designed to amplify DCs via the application of biomaterials are discussed with the aim of inspiring the clinical translation of future DC-mediated cancer immunotherapies.

Indexed as

ImmunotherapyNeoplasmsAntigen PresentationBiocompatible MaterialsDendritic CellsImmunosuppression TherapyBiocompatible Materialsbiomaterialscancer immunotherapydendritic cellsnanovaccinetumor microenvironment

Identifiers

PMID37088780
PMCPMC10288267
OpenAlexW4366782961

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.