Evidence map›Paper›PMID 25354725›Full record

ArticleNature communications2014

Clearance of persistent HPV infection and cervical lesion by therapeutic DNA vaccine in CIN3 patients.

Tae Jin Kim, Hyun-Tak Jin, Soo-Young Hur, Hyun Gul Yang, Yong Bok Seo, Sung Ran Hong, Chang-Woo Lee, Suhyeon Kim, Jung-Won Woo, Ki Seok Park and 10 more

Open access · hybridAbstract readClinical Trial, Phase I
In one paragraph

Article in Nature communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 1 pooled it
13.7field-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

131 citing papers in PubMed, 1 synthesis or guideline pooled it, 255 citations in OpenAlex.

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  15. bioRxiv : the preprint server for biology · 2025
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  20. Cancer vaccines: current status and future directions.Journal of hematology & oncology · 2025
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71 more citing papers are in PubMed but not listed here.

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

20 authors at 6 institutions in 1 country.

Tae Jin KimDepartment of Obstetrics and Gynecology, Cheil General Hospital and Women's Healthcare Center, College of Medicine, Kwandong University, Seoul 100-380, Korea.
Hyun-Tak JinResearch Institute, Genexine Inc., Korea Bio Park, Seongnam, Gyeonggi-do 463-400, Korea.
Soo-Young HurDepartment of Obstetrics and Gynecology, Seoul St Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 137-701, Korea.
Hyun Gul YangDivision of Integrative Bioscience and Biotechnology, Pohang University of Science and Technology, Pohang 790-784, Korea.
Yong Bok SeoDivision of Integrative Bioscience and Biotechnology, Pohang University of Science and Technology, Pohang 790-784, Korea.
Sung Ran HongDepartment of Pathology, Cheil General Hospital and Women's Healthcare Center, College of Medicine, Kwandong University, Seoul 100-380, Korea.
Chang-Woo LeeDepartment of Molecular Cell Biology, Samsung Biomedical Research Institute, Sungkyunkwan University School of Medicine, Suwon, Gyeonggi-do 440-746, Korea.
Suhyeon KimDepartment of Molecular Cell Biology, Samsung Biomedical Research Institute, Sungkyunkwan University School of Medicine, Suwon, Gyeonggi-do 440-746, Korea.
Jung-Won WooResearch Institute, Genexine Inc., Korea Bio Park, Seongnam, Gyeonggi-do 463-400, Korea.
Ki Seok ParkResearch Institute, Genexine Inc., Korea Bio Park, Seongnam, Gyeonggi-do 463-400, Korea.
Youn-Young HwangResearch Institute, Genexine Inc., Korea Bio Park, Seongnam, Gyeonggi-do 463-400, Korea.
Jaehan ParkResearch Institute, Genexine Inc., Korea Bio Park, Seongnam, Gyeonggi-do 463-400, Korea.
In-Ho LeeDepartment of Obstetrics and Gynecology, Cheil General Hospital and Women's Healthcare Center, College of Medicine, Kwandong University, Seoul 100-380, Korea.
Kyung-Taek LimDepartment of Obstetrics and Gynecology, Cheil General Hospital and Women's Healthcare Center, College of Medicine, Kwandong University, Seoul 100-380, Korea.
Ki-Heon LeeDepartment of Obstetrics and Gynecology, Cheil General Hospital and Women's Healthcare Center, College of Medicine, Kwandong University, Seoul 100-380, Korea.
Mi Seon JeongLaboratory of R&D for Genomics, Cheil General Hospital and Women's Healthcare Center, College of Medicine, Kwandong University, Seoul 100-380, Korea.
Charles D Surh1] Division of Integrative Bioscience and Biotechnology, Pohang University of Science and Technology, Pohang 790-784, Korea [2] Academy of Immunology and Microbiology, Institute of Basic Science, Pohang 790-784, Korea.
You Suk SuhResearch Institute, Genexine Inc., Korea Bio Park, Seongnam, Gyeonggi-do 463-400, Korea.
Jong Sup ParkDepartment of Obstetrics and Gynecology, Seoul St Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 137-701, Korea.
Young Chul Sung1] Research Institute, Genexine Inc., Korea Bio Park, Seongnam, Gyeonggi-do 463-400, Korea [2] Division of Integrative Bioscience and Biotechnology, Pohang University of Science and Technology, Pohang 790-784, Korea.
Genexine (South Korea) · KRPohang University of Science and Technology · KRCatholic Kwandong University · KRCheil General Hospital and Women's Healthcare Center · KRCatholic University of Korea · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we demonstrate that electroporation-enhanced immunization with a rationally designed HPV DNA vaccine (GX-188E), preferentially targeting HPV antigens to dendritic cells, elicits a significant E6/E7-specific IFN-γ-producing T-cell response in all nine cervical intraepithelial neoplasia 3 (CIN3) patients. Importantly, eight out of nine patients exhibit an enhanced polyfunctional HPV-specific CD8 T-cell response as shown by an increase in cytolytic activity, proliferative capacity and secretion of effector molecules. Notably, seven out of nine patients display complete regression of their lesions and viral clearance within 36 weeks of follow up. GX-188E administration does not elicit serious vaccine-associated adverse events at all administered doses. These findings indicate that the magnitude of systemic polyfunctional CD8 T-cell response is the main contributing factor for histological, cytological and virological responses, providing valuable insights into the design of therapeutic vaccines for effectively treating persistent infections and cancers in humans.

Indexed as

AdultAntibody FormationCD8-Positive T-LymphocytesFemaleHumansImmunity, CellularMiddle AgedOncogene Proteins, ViralPapillomavirus InfectionsPapillomavirus VaccinesUterine Cervical DysplasiaUterine Cervical NeoplasmsVaccines, DNAYoung AdultGX-188 vaccineOncogene Proteins, ViralPapillomavirus VaccinesVaccines, DNA

Identifiers

PMID25354725
PMCPMC4220493
OpenAlexW2080731494

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.