Evidence map›Paper›PMID 25701675›Full record

ArticleVaccine2015

Local administration of granulocyte macrophage colony-stimulating factor induces local accumulation of dendritic cells and antigen-specific CD8+ T cells and enhances dendritic cell cross-presentation.

Sung-Jong Lee, Liwen Song, Ming-Chieh Yang, Chih-Ping Mao, Benjamin Yang, Andrew Yang, Jessica Jeang, Shiwen Peng, T-C Wu, Chien-Fu Hung

Abstract read
In one paragraph

Article in Vaccine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Activities of stromal and immune cells in HPV-related cancers.Journal of experimental & clinical cancer research : CR · 2018
    Review
  9. Review
  10. Modulation of antigen presenting cell functions during chronic HPV infection.Papillomavirus research (Amsterdam, Netherlands) · 2017
    Review
  11. Article
  12. Review
  13. 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

10 authors at 2 institutions in 4 countries.

Sung-Jong LeeDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States; Department of Obstetrics and Gynecology, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Republic of Korea.
Liwen SongDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States; Pharmacy School of Fudan University, Shanghai, China; Department of Obstetrics and Gynecology, Shanghai Tenth People's Hospital of Tongji University, Shanghai, China; Department of Pharmacology and Toxicology, Shanghai Institute of Planned Parenthood Research, Shanghai, China.
Ming-Chieh YangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States; Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Chih-Ping MaoDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
Benjamin YangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
Andrew YangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
Jessica JeangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
Shiwen PengDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
T-C WuDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States; Departments of Obstetrics and Gynecology, Johns Hopkins Medical Institutions, Baltimore, MD, United States; Departments of Molecular Microbiology and Immunology, Johns Hopkins Medical Institutions, Baltimore, MD, United States; Department of Oncology, Johns Hopkins Medical Institutions, Baltimore, MD, United States.
Chien-Fu HungDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, United States; Department of Oncology, Johns Hopkins Medical Institutions, Baltimore, MD, United States. Electronic address: chung2@jhmi.edu.
Johns Hopkins University · USKaohsiung Veterans General Hospital · 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
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007309 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 1985 to 2019
$43.2M
CELLULAR &MOLECULAR MECH OF INFLAMMATORY REACTIONST32AI007247 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Joel L Pomerantz · 1985 to 2026
$10.2M
ENHANCING HPV-16 E6-SPECIFIC ANTITUMOR IMMUNITYR01CA114425 · NCI · JOHNS HOPKINS UNIVERSITY · PI WU, TZYY-CHOOU · 2005 to 2016
$3.0M
Research Pilot Project 2P20CA192988 · NCI · JOHNS HOPKINS UNIVERSITY · PI CALIFANO, JOSEPH A · 2014 to 2017
$702k
NCI NIH HHS 1P20CA192988-01NCI NIH HHS P20 CA192988NCI NIH HHS P50 CA098252NCI NIH HHS R01 CA114425NCI NIH HHS R01 CA114425-01NIAID NIH HHS T32 AI007247NIGMS NIH HHS T32 GM007309
6 · The paper itself

Abstract

Immunotherapy has emerged as a promising treatment strategy for the control of HPV-associated malignancies. Various therapeutic HPV vaccines have elicited potent antigen-specific CD8+ T cell mediated antitumor immune responses in preclinical models and are currently being tested in several clinical trials. Recent evidence indicates the importance of local immune activation, and higher number of immune cells in the site of lesion correlates with positive prognosis. Granulocyte macrophage colony-stimulating factor (GMCSF) has been reported to posses the ability to induce migration of antigen presentation cells and CD8+ T cells. Therefore, in the current study, we employ a combination of systemic therapeutic HPV DNA vaccination with local GMCSF application in the TC-1 tumor model. We show that intramuscular vaccination with CRT/E7 DNA followed by GMCSF intravaginal administration effectively controls cervicovaginal TC-1 tumors in mice. Furthermore, we observe an increase in the accumulation of E7-specific CD8+ T cells and dendritic cells in vaginal tumors following the combination treatment. In addition, we show that GMCSF induces activation and maturation in dendritic cells and promotes antigen cross-presentation. Our results support the clinical translation of the combination treatment of systemic therapeutic vaccination followed by local GMCSF administration as an effective strategy for tumor treatment.

Indexed as

Administration, IntravaginalAnimalsAntigen-Presenting CellsCancer VaccinesCD8-Positive T-LymphocytesCombined Modality TherapyCross-PrimingDendritic CellsFemaleGranulocyte-Macrophage Colony-Stimulating FactorImmunotherapyInjections, IntramuscularMiceMice, Inbred C57BLPapillomavirus VaccinesUterine Cervical NeoplasmsCancer VaccinesGranulocyte-Macrophage Colony-Stimulating FactorPapillomavirus VaccinesCRT/E7Dendritic cellGM-CSFImmunotherapy

Identifiers

PMID25701675
PMCPMC4361388
OpenAlexW2007895035

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.