Evidence map›Paper›PMID 38962939›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Dendritic Cell-Hitchhiking In Vivo for Vaccine Delivery to Lymph Nodes.

Lei Zhou, Ling Zhao, Mengyao Wang, Xu Qi, Xin Zhang, Qingying Song, Dayu Xue, Meihua Mao, Zhenzhong Zhang, Jinjin Shi and 2 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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  13. Dendritic Cell-Hitchhiking In Vivo for Vaccine Delivery to Lymph Nodes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

12 authors.

Lei ZhouSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Ling ZhaoSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Mengyao WangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Xu QiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Xin ZhangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Qingying SongSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Dayu XueSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Meihua MaoSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Zhenzhong ZhangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Jinjin ShiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Pilei SiDepartment of Breast Surgery, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, People's Hospital of Henan University, Zhengzhou, Henan, 450003, China.
Junjie LiuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.ORCID 0000-0002-9404-050X

Funding

Henan Science Fund for Outstanding Young Scholars 232300421051National Natural Science Foundation of China 82172762National Natural Science Foundation of China 82373287Science and technology innovation talents support project of Henan Province 23HASTIT041
6 · The paper itself

Abstract

Therapeutic cancer vaccines are among the first FDA-approved cancer immunotherapies. Among them, it remains a major challenge to achieve robust lymph-node (LN) accumulation. However, delivering cargo into LN is difficult owing to the unique structure of the lymphatics, and clinical responses have been largely disappointing. Herein, inspired by the Migrated-DCs homing from the periphery to the LNs, an injectable hydrogel-based polypeptide vaccine system is described for enhancing immunostimulatory efficacy, which could form a local niche of vaccine "hitchhiking" on DCs. The OVA peptide modified by lipophilic DSPE domains in the hydrogel is spontaneously inserted into the cell membrane to achieve "antigen anchoring" on DCs in vivo. Overall, OVA peptide achieves active access LNs through recruiting and "hitchhiking" subcutaneous Migrated-DCs. Remarkably, it is demonstrated that the composite hydrogel enhances LNs targeting efficacy by approximately six-fold compared to free OVA peptide. Then, OVA peptide can be removed from the cell surface under a typical acidic microenvironment within the LNs, further share them with LN-resident APCs via the "One-to-Many" strategy (One Migrated-DC corresponding to Many LN-resident APCs), thereby activating powerful immune stimulation. Moreover, the hydrogel vaccine exhibits significant tumor growth inhibition in melanoma and inhibits pulmonary metastatic nodule formation.

Indexed as

Cancer VaccinesDendritic CellsLymph NodesAnimalsDisease Models, AnimalFemaleHydrogelsImmunotherapyMiceMice, Inbred C57BLOvalbuminCancer VaccinesHydrogelsOvalbumindendritic cell‐hitchhikinglymph node targetingvaccine delivery

Identifiers

PMID38962939
PMCPMC11434131

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Registered trials

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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.