Evidence map›Paper›PMID 29414659›Full record

ArticleInternational immunopharmacology2018

Evaluation of immune responses induced by a novel human papillomavirus type 16 E7 peptide-based vaccine with Candida skin test reagent as an adjuvant in C57BL/6 mice.

Xingxuan Wang, Yuxin Che, Bingnan Chen, Yao Zhang, Mayumi Nakagawa, Xuelian Wang

Open access · greenAbstract read
In one paragraph

Article in International immunopharmacology, 2018. 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
1.8field-weighted citation impact, top 16% 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, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. The role of Tim-3/Galectin-9 pathway in T-cell function and prognosis of patients with human papilloma virus-associated cervical carcinoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  7. Article
  8. 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

6 authors at 3 institutions in 2 countries.

Xingxuan WangDepartment of Microbiology and Parasitology, College of Basic Medical Sciences, China Medical University, Shenyang, China.
Yuxin CheDepartment of Microbiology and Parasitology, College of Basic Medical Sciences, China Medical University, Shenyang, China.
Bingnan ChenThe 3rd Clinical Department, China Medical University, Shenyang, China.
Yao ZhangThe 3rd Clinical Department, China Medical University, Shenyang, China.
Mayumi NakagawaDepartment of Pathology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: MNakagawa@uams.edu.
Xuelian WangDepartment of Microbiology and Parasitology, College of Basic Medical Sciences, China Medical University, Shenyang, China. Electronic address: xlwang18@cmu.edu.cn.
China Medical University · CNUniversity of Arkansas for Medical Sciences · USUniversity of Arkansas Medical Center · US

Funding

Understanding and Enhancing T-Cell Responses to High Risk Human Papillomaviruses-RenewalR01CA143130 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI NAKAGAWA, MAYUMI · 2010 to 2025
$10.0M
NCI NIH HHS R01 CA143130
6 · The paper itself

Abstract

Cell mediated immune (CMI) responses are crucial for the clearance of human papillomavirus (HPV) infection and HPV-associated lesions. Activated CD8 T cells are critical effector cells in recognizing and killing HPV-infected or HPV-transformed cells. CD4 T cells provide help for priming the generation and maintenance of CD8 T cells as well as for tumors immunity. An ideal therapeutic HPV peptide-based vaccine should induce both a robust CD8 T-cell response as well as a CD4 T-cell response for ensuring their efficiency. Candida skin test reagent was demonstrated to be able to induce the secretion of IL-12 by Langerhans cells and T-cell proliferation in vitro by our group, which indicated the potential of Candida to enhance CMI response. In this current study, we designed a novel HPV peptide-based vaccine which includes HPV16 E7 peptides and Candida as an adjuvant. The immune responses induced by the vaccine were comprehensively evaluated. The results showed that the vaccine induced significant HPV-specific CD8 T-cell and Th1 CD4 T-cell responses as well as humoral immune response. It is interesting that Candida alone induced a significant polarization of Th1 response an production of IFN-γ, which indicated Candida alone may be used as a potential immunotherapeutic reagent not only for HPV-associated lesions but also for other viral infection or even cancers.

Indexed as

Adjuvants, ImmunologicAnimalsCandidaCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationCells, CulturedEpitopes, T-LymphocyteHuman papillomavirus 16HumansImmunity, HumoralInterleukin-12Langerhans CellsMiceMice, Inbred C57BLPapillomavirus E7 ProteinsAdjuvants, ImmunologicEpitopes, T-LymphocyteInterleukin-12oncogene protein E7, Human papillomavirus type 16Papillomavirus E7 ProteinsPapillomavirus VaccinesAdjuvantCandidaE7Human papillomavirusPeptideVaccine

Identifiers

PMID29414659
PMCPMC5967262
OpenAlexW2792496568

What OpenQuestion holds

Textmetadata
LicenceTDM
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.