Evidence map›Paper›PMID 42236671›Full record

ArticleSignal transduction and targeted therapy2026

Innovative peptide-loaded hybrid membrane nanovaccine enables precise personalized immunotherapy for HPV-related cervical diseases.

Renjie Wang, Jie Wang, Jinghan Ruan, Chun Gao, Bai Hu, Liang Chen, Bingqing Liao, Ding Ma, Shuguang Tan, Yuanzhen Zhang and 1 more

Abstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Renjie Wang *Department of Obstetrics and Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Jie Wang *Innovative Vaccine and Immunotherapy Research Center, The Second Affiliated Hospital , Zhejiang University School of Medicine, Hangzhou, China.
Jinghan Ruan *Department of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Chun GaoDepartment of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Bai HuDepartment of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Liang ChenDepartment of Obstetrics and Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Bingqing LiaoDepartment of Obstetrics and Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Ding MaDepartment of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Shuguang TanInnovative Vaccine and Immunotherapy Research Center, The Second Affiliated Hospital , Zhejiang University School of Medicine, Hangzhou, China. tansg@zju.edu.cn.ORCID http://orcid.org/0000-0002-2599-4959
Yuanzhen ZhangDepartment of Obstetrics and Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China. zhangyuanzhen@whu.edu.cn.
Shujie LiaoDepartment of Obstetrics and Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China. liaosjmailbox@126.com.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82341120National Natural Science Foundation of China (National Science Foundation of China) 82372354National Natural Science Foundation of China (National Science Foundation of China) 82501971
6 · The paper itself

Abstract

Human papillomavirus (HPV)-associated cervical diseases pose significant health risks to women worldwide. Current clinical interventions face challenges in achieving complete viral clearance and controlling disease progression, with limited efficacy and recurrence risks. To address this unmet need, we developed an innovative nanovaccine (HM-NPs@LP) designed to codeliver tumor cell membranes (TMs), bacterial cytoplasmic membranes (EMs), and HPV16 long peptides (LP) through PLGA nanoparticles to elicit antitumor immunity. HPV16 E5/E6/E7 LP and TM provide individualized broad-spectrum antigen repertoires, including tumor-specific and tumor-associated antigens. EMs serve as natural adjuvants to enhance immunogenicity. The resulting nanovaccine demonstrates uniform nanoparticles (177 nm) with excellent stability and biosafety. In vitro, HM-NPs@LP exhibited efficient uptake by bone marrow-derived dendritic cells (BMDCs), which in turn promoted DC maturation and strengthened tumor-specific T-cell responses. In vivo studies in murine models demonstrate that HM-NPs@LP preferentially accumulate in lymph nodes and elicit potent tumor suppression. Furthermore, this vaccination induces durable immune memory to prevent tumor recurrence with minimal systemic toxicity. Additionally, humanized HLA-A*02:01 transgenic mice mirror these therapeutic outcomes. Synergy with taxane-platinum (TP) chemotherapy and anti-PD-1 immunotherapy further augments tumor regression. Overall, the scalable production, biosafety, and adaptability for personalized immunotherapy position this nanovaccine platform as a promising therapeutic strategy for the treatment of HPV-related cervical diseases and potentially other malignancies.

Indexed as

Cancer VaccinesHuman papillomavirus 16ImmunotherapyPapillomavirus InfectionsUterine Cervical NeoplasmsAnimalsDendritic CellsFemaleHumansMiceNanoparticlesNanovaccinesPeptidesPrecision MedicineProtein Subunit VaccinesCancer VaccinesNanovaccinesPeptidesProtein Subunit Vaccines

Identifiers

PMID42236671
PMCPMC13233851

What OpenQuestion holds

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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.