Evidence map›Paper›PMID 28423693›Full record

ArticleOncotarget2017

Enhanced anti-tumor therapeutic efficacy of DNA vaccine by fusing the E7 gene to BAFF in treating human papillomavirus-associated cancer.

Chao-Chih Wu, Fang-Cih Wu, Yun-Tin Hsu, Yu-Chia Hsiao, Yuh-Cheng Yang, C Allen Chang, Chih-Long Chang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Advances in nucleic acid-based cancer vaccines.Journal of biomedical science · 2025
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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

7 authors at 2 institutions in 1 country.

Chao-Chih WuDepartmental of Medical Research, Mackay Memorial Hospital, New Taipei City, Taiwan.
Fang-Cih WuDepartmental of Medical Research, Mackay Memorial Hospital, New Taipei City, Taiwan.
Yun-Tin HsuDepartmental of Medical Research, Mackay Memorial Hospital, New Taipei City, Taiwan.
Yu-Chia HsiaoDepartmental of Medical Research, Mackay Memorial Hospital, New Taipei City, Taiwan.
Yuh-Cheng YangDepartment of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei City, Taiwan.
C Allen ChangDepartment of Biotechnology and Laboratory Science in Medicine, School of Biomedical Science and Engineering, National Yang-Ming University, Taipei City, Taiwan.
Chih-Long ChangDepartment of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei City, Taiwan.
Mackay Memorial Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B-cell-activating factor (BAFF) belongs to the tumor necrosis factor family that not only stimulates B and T cells but also counteracts immune tolerance. BAFF is also a type II membrane protein, which is secreted through the endoplasmic reticulum (ER)-Golgi apparatus pathway. Fusing an antigen to BAFF might enhance the presentation of major histocompatibility complex class I molecules. These characteristics represent an opportunity to enhance the antitumor effects of DNA vaccines. Therefore, we fused BAFF to human papillomavirus type 16 E7 as a DNA vaccine and evaluated its antitumor effects. We found that this vaccine increased E7-specific CD8+ T-cell immune responses, engendered major antitumor effects against E7-expressing tumors, and prolonged the survival of the immunized mice. Interestingly, vaccinating B-cell-deficient mice with BAFF-E7 revealed considerable E7-specific CD8+ T-cell immune responses, suggesting that B cells do not contribute to this immune response. Image analysis through confocal fluorescence microscopy revealed that fusing BAFF to E7 targeted the protein to the ER, but not BAFF lacking 128 N-terminal residues that generated a lower number of E7-specific CD8+ T cells in the vaccinated mice. Our data indicated that the ER-targeting characteristic of BAFF is the main factor improving the potency of DNA vaccines.

Indexed as

AnimalsB-Cell Activating FactorCancer VaccinesCarcinoma, Non-Small-Cell LungCD8-Positive T-LymphocytesCell Line, TumorFemaleHumansLung NeoplasmsMicePapillomaviridaePapillomavirus E7 ProteinsPapillomavirus InfectionsRecombinant Fusion ProteinsVaccines, DNAXenograft Model Antitumor AssaysB-Cell Activating FactorCancer VaccinesPapillomavirus E7 ProteinsRecombinant Fusion ProteinsTNFSF13B protein, humanVaccines, DNABAFFDNA vaccine

Identifiers

PMID28423693
PMCPMC5464847
OpenAlexW2593171619

What OpenQuestion holds

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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.