Evidence map›Paper›PMID 19454266›Full record

ReviewExperimental and molecular pathology2009

ProtEx technology for the generation of novel therapeutic cancer vaccines.

Rich-Henry Schabowsky, Rajesh K Sharma, Shravan Madireddi, Abhishek Srivastava, Esma S Yolcu, Haval Shirwan

Open access · greenAbstract readReview
In one paragraph

Review in Experimental and molecular pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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 1 country.

Rich-Henry SchabowskyDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY 40202, USA.
Rajesh K Sharma
Shravan Madireddi
Abhishek Srivastava
Esma S Yolcu
Haval Shirwan
University of Louisville · USJames Graham Brown Foundation · US

Funding

ApoVax104-HPV as a Novel Vaccine for Cervical CancerR44AI071618 · NIAID · APOVAX, INC. · PI MACLEOD, KATHRYN J, SHIRWAN, HAVAL · 2008 to 2009
$1.8M
Allograft Tolerance with Fas/FasL-Mediated ApoptosisR01AI047864 · NIAID · UNIVERSITY OF LOUISVILLE · PI SHIRWAN, HAVAL · 2002 to 2005
$1.1M
A Novel Approach to Prevent and Treat Type 1 DiabetesR21AI057903 · NIAID · UNIVERSITY OF LOUISVILLE · PI SHIRWAN, HAVAL · 2004 to 2005
$588k
Engineering Bone Marrow Cells for ImmunotherapyR21HL080108 · NHLBI · UNIVERSITY OF LOUISVILLE · PI YOLCU, ESMA S · 2005 to 2006
$399k
ApoVax-SVN as a Novel Vaccine for Cancer ImmunotherapyR41CA121665 · NCI · APOVAX, INC. · PI SHIRWAN, HAVAL · 2007 to 2007
$328k
ApoVax104-HPV as a Novel Vaccine for Cervical CancerR43AI071618 · NIAID · APOVAX, INC. · PI MACLEOD, KATHRYN J. · 2007 to 2007
$300k
NCI NIH HHS R41 CA121665NCI NIH HHS R41CA121665NHLBI NIH HHS R21 HL080108NHLBI NIH HHS R21HL080108NIAID NIH HHS R01 AI047864NIAID NIH HHS R01AI47864NIAID NIH HHS R21 AI057903NIAID NIH HHS R21AI057903NIAID NIH HHS R43 AI071618NIAID NIH HHS R43AI071618NIAID NIH HHS R44 AI071618NIAID NIH HHS R44AI071618
6 · The paper itself

Abstract

Therapeutic vaccines present an attractive alternative to conventional treatments for cancer. However, tumors have evolved various immune evasion mechanisms to modulate innate, adaptive, and regulatory immunity for survival. Therefore, successful vaccine formulations may require a non-toxic immunomodulator or adjuvant that not only induces/stimulates innate and adaptive tumor-specific immune responses, but also overcomes immune evasion mechanisms. Given the paramount role costimulation plays in modulating innate, adaptive, and regulatory immune responses, costimulatory ligands may serve as effective immunomodulating components of therapeutic cancer vaccines. Our laboratory has developed a novel technology designated as ProtEx that allows for the generation of recombinant costimulatory ligands with potent immunomodulatory activities and the display of these molecules on the cell surface in a rapid and efficient manner as a practical and safe alternative to gene therapy for immunomodulation. Importantly, the costimulatory ligands not only function when displayed on tumor cells, but also as soluble proteins that can be used as immunomodulatory components of conventional vaccine formulations containing tumor-associated antigens (TAAs). We herein discuss the application of the ProtEx technology to the development of effective cell-based as well as cell-free conventional therapeutic cancer vaccines.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, NeoplasmBiotechnologyCancer VaccinesDendritic CellsGenetic EngineeringGenetic TherapyHumansNeoplasmsSolubilityToll-Like ReceptorsAdjuvants, ImmunologicAntigens, NeoplasmCancer VaccinesToll-Like Receptors

Identifiers

PMID19454266
PMCPMC2917214
OpenAlexW2078046563

What OpenQuestion holds

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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.