Evidence map›Paper›PMID 19056449›Full record

ArticleVaccine2009

Enhancing therapeutic HPV DNA vaccine potency through depletion of CD4+CD25+ T regulatory cells.

Chi-Mu Chuang, Talia Hoory, Archana Monie, Annie Wu, Mei-Cheng Wang, Chien-Fu Hung

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 51 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Therapeutic vaccines for high-risk HPV-associated diseases.Papillomavirus research (Amsterdam, Netherlands) · 2018
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. HPV infection: immunological aspects and their utility in future therapy.Infectious diseases in obstetrics and gynecology · 2013
    Review
  15. Article
  16. Vaccination in the elderly.Microbial biotechnology · 2012
    Review
  17. Article
  18. Article
  19. Article
  20. 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 2 institutions in 2 countries.

Chi-Mu ChuangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Talia Hoory
Archana Monie
Annie Wu
Mei-Cheng Wang
Chien-Fu Hung
Johns Hopkins University · USNational Yang Ming Chiao Tung University · TW

Funding

Treatment of HIV- and HIV+ Patients with HPV16+ CIN2/3 Using pNGLV4a-hCRTE6E7L2 DNA vaccine administered intramuscularly via electroporationP50CA098252 · NCI · JOHNS HOPKINS UNIVERSITY · PI TZYY-CHOOU WU · 2003 to 2026
$53.5M
ENHANCING HPV-16 E6-SPECIFIC ANTITUMOR IMMUNITYR01CA114425 · NCI · JOHNS HOPKINS UNIVERSITY · PI WU, TZYY-CHOOU · 2005 to 2016
$3.0M
NCI NIH HHS 1 R01 CA114425 01NCI NIH HHS P50 CA098252NCI NIH HHS R01 CA114425
6 · The paper itself

Abstract

Therapeutic human papillomavirus (HPV) vaccines targeting E6 and/or E7 antigens represent an opportunity to control HPV-associated lesions. We have previously generated several therapeutic DNA vaccines targeting HPV-16 E7 antigen and generated significant antitumor effects. Since regulatory T cells (Tregs) play an important role in suppressing immune responses against tumors by immunotherapy, such as DNA vaccines, we tested if the therapeutic effects of a DNA vaccine encoding E7 linked to heat shock protein 70 (Hsp70) can be improved by a strategy to deplete Tregs using a anti-CD25 monoclonal antibody (PC61) in vaccinated mice. We found that administration of PC61 prior to vaccination with E7/Hsp70 DNA was capable of generating higher levels of E7-specific CD8(+) T cells compared to the control antibody, leading to significantly improved therapeutic and long-term protective antitumor effects against an E7-expressing tumor, TC-1. Thus, a strategy to deplete CD4(+)CD25(+) Tregs in conjunction with therapeutic tumor antigen-specific DNA vaccine may represent a potentially promising approach to control tumor. The clinical implications of our study are discussed.

Indexed as

Lymphocyte DepletionAnimalsCancer VaccinesCD8-Positive T-LymphocytesFemaleHSP72 Heat-Shock ProteinsHumansImmunotherapy, ActiveMiceMice, Inbred C57BLNeoplasmsPapillomavirus VaccinesSurvival AnalysisT-Lymphocytes, RegulatoryVaccines, DNAVaccines, SyntheticCancer VaccinesHSP72 Heat-Shock ProteinsPapillomavirus VaccinesVaccines, DNAVaccines, Synthetic

Identifiers

PMID19056449
PMCPMC2658755
OpenAlexW2003084998

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.