Evidence map›Paper›PMID 21839051›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2012

Structure and biological activity of pathogen-like synthetic nanomedicines.

Orsolya Lőrincz, Enikő R Tőke, Eszter Somogyi, Ferenc Horkay, Preethi L Chandran, Jack F Douglas, János Szebeni, Julianna Lisziewicz

4 registry-linked trialsAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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.

NCT00270205 phase1 / phase2completednot on this map

A Phase I/II, Randomized, Double-Blind Study to Evaluate the Safety, Tolerability, and Immunogenicity of LC002, a DermaVir Vaccine, in HIV-1-Infected Subjects Currently Under Treatment With Highly Active Antiretroviral Therapy (HAART)

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2006 to 2010Enrolled28ConditionsHIV InfectionsArmsLC002 standard vaccination, LC002 high-dose vaccination, LC002 placebo vaccination
NCT00711230 phase2completednot on this map

A Phase II Randomized, Placebo-Controlled, Multi-Center Study to Evaluate the Safety, Tolerability, Immunogenicity, and Antiretroviral Activity of DermaVir Patch (LC002) in Treatment-Naïve HIV-1-Infected Patients

TypeinterventionalSponsorGenetic ImmunityRan2008 to 2015Enrolled36ConditionsHIV InfectionArmsDermaVir, Placebo
NCT00712530 phase1completednot on this map

A Phase I Study to Evaluate the Tolerability and Safety of LC002, a DermaVir Vaccine, in HIV-1-infected Subjects Currently Under Treatment With Highly Active Antiretroviral Therapy (HAART)

TypeinterventionalSponsorGenetic ImmunityRan2005 to 2006Enrolled9ConditionsHIV InfectionArmsDermaVir, HAART
NCT00918840 completednot on this map

Antiretroviral-Sparing Concept: An Exploratory Phase II, Randomized, Single Blind Placebo-Controlled Study to Investigate the Effect of Therapeutic Immunization on the Quantity of HIV-Specific T Cell Precursors During Highly Active Antiretroviral Therapy Followed by Analytical Treatment Interruption

TypeobservationalSponsorGenetic ImmunityRan2009 to 2011Enrolled16ConditionsHIV InfectionArmsDermaVir, Placebo, HAART
3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Establishing Rules for Self-Adhesion and Aggregation ofLangmuir : the ACS journal of surfaces and colloids · 2020
    Article
  5. Review
  6. Review
  7. Nanostructures for the Inhibition of Viral Infections.Molecules (Basel, Switzerland) · 2015
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  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

8 authors.

Orsolya LőrinczGenetic Immunity Kft, Budapest, Berlini u., Hungary.
Enikő R Tőke
Eszter Somogyi
Ferenc Horkay
Preethi L Chandran
Jack F Douglas
János Szebeni
Julianna Lisziewicz

Funding

Water-Ion-Biopolymer InteractionsZIAHD008756 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BASSER, PETER J. · 2009 to 2017
$2.4M
Intramural NIH HHS ZIA HD008756
6 · The paper itself

Abstract

Here we characterize the structure, stability and intracellular mode of action of DermaVir nanomedicine that is under clinical development for the treatment of HIV/AIDS. This nanomedicine comprises pathogen-like pDNA/PEIm nanoparticles (NPs) having the structure and function resembling spherical viruses that naturally evolved to deliver nucleic acids to the cells. Atomic force microscopy demonstrated spherical 100 - 200 nm NPs with a smooth polymer surface protecting the pDNA in the core. Optical absorption determined both the NP structural stability and biological activity relevant to their ability to escape from the endosome and release the pDNA at the nucleus. Salt, pH and temperature influence nanomedicine shelf-life and intracellular stability. This approach facilitates the development of diverse polyplex nanomedicines where the delivered pDNA-expressed antigens induce immune responses to kill infected cells. FROM THE CLINICAL EDITOR: The authors investigated DermaVir nanomedicine comprised of pathogen-like pDNA/PEIm nanoparticles with structure and function resembling spherical viruses. DermaVir delivery of pDNA expresses antigens that induce immune responses to kill HIV infected cells.

Indexed as

AIDS VaccinesCell NucleusDNAHIV-1NanoparticlesAcquired Immunodeficiency SyndromeCell LineHumansParticle SizeTransfectionAIDS VaccinesDermaVirDNA

Identifiers

PMID21839051
PMCPMC3274662

What OpenQuestion holds

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Registered trials

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.