Evidence map›Paper›PMID 38715363›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

Development of an mRNA-based therapeutic vaccine mHTV-03E2 for high-risk HPV-related malignancies.

Jing Wang, Qixin Wang, Ling Ma, Kai Lv, Lu Han, Yunfeng Chen, Rui Zhou, Haokun Zhou, Hua Chen, Yi Wang and 11 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
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  8. Circular RNA-based HPV16 therapeutic vaccine elicits potent and durable antitumor immunity.Journal of experimental & clinical cancer research : CR · 2026
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  11. Review
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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

21 authors.

Jing WangInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Qixin WangRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Ling MaInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Kai LvInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Lu HanRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Yunfeng ChenRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Rui ZhouInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Haokun ZhouRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Hua ChenRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Yi WangRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Tingting ZhangRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Dongrong YiInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Qian LiuInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Yongxin ZhangInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Xiaoyu LiInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Tingting ChengInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Jinming ZhangRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Chunjian HuangRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China.
Yijie DongRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China. Electronic address: yijie.dong@rinuagene.com.
Weiguo ZhangRinuaGene Biotechnology Co., Ltd., Suzhou 215127, China. Electronic address: weiguo.zhang@rinuagene.com.
Shan CenInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China. Electronic address: shancen@imb.pumc.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human papillomavirus (HPV) 16 and 18 infections are related to many human cancers. Despite several preventive vaccines for high-risk (hr) HPVs, there is still an urgent need to develop therapeutic HPV vaccines for targeting pre-existing hrHPV infections and lesions. In this study, we developed a lipid nanoparticle (LNP)-formulated mRNA-based HPV therapeutic vaccine (mHTV)-03E2, simultaneously targeting the E2/E6/E7 of both HPV16 and HPV18. mHTV-03E2 dramatically induced antigen-specific cellular immune responses, leading to significant CD8

Indexed as

Oncogene Proteins, ViralPapillomavirus InfectionsPapillomavirus VaccinesRNA, MessengerAnimalsCancer VaccinesCD8-Positive T-LymphocytesCell Line, TumorDisease Models, AnimalDNA-Binding ProteinsFemaleHuman papillomavirus 16Human papillomavirus 18HumansLiposomesMiceCancer VaccinesDNA-Binding ProteinsE6 protein, Human papillomavirus type 16E6 protein, Human papillomavirus type 18Lipid NanoparticlesLiposomesoncogene protein E7, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus E7 ProteinsPapillomavirus VaccinesRepressor ProteinsRNA, Messengeranimal modelcheckpoint blockadeHPVmRNA therapeutic vaccinetumor

Identifiers

PMID38715363
PMCPMC11286823

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.