Evidence map›Paper›PMID 27389189›Full record

ArticleNanomedicine (London, England)2016

Conjugating Prussian blue nanoparticles onto antigen-specific T cells as a combined nanoimmunotherapy.

Rachel A Burga, Shabnum Patel, Catherine M Bollard, Conrad Russell Y Cruz, Rohan Fernandes

Abstract read
In one paragraph

Article in Nanomedicine (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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.

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

19 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. [MnNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  7. Review
  8. Review
  9. Review
  10. International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2020
    Review
  11. Article
  12. Immunologically modified MnFeChemical engineering journal (Lausanne, Switzerland : 1996) · 2020
    Article
  13. Advanced biomaterials for cancer immunotherapy.Acta pharmacologica Sinica · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Gold nanoparticle-mediated photothermal therapy: applications and opportunities for multimodal cancer treatment.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
  18. Delivering safer immunotherapies for cancer.Advanced drug delivery reviews · 2017
    Review
  19. 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

5 authors.

Rachel A BurgaInstitute for Biomedical Sciences, The George Washington University, Washington, DC, USA.
Shabnum PatelInstitute for Biomedical Sciences, The George Washington University, Washington, DC, USA.
Catherine M BollardInstitute for Biomedical Sciences, The George Washington University, Washington, DC, USA.
Conrad Russell Y CruzInstitute for Biomedical Sciences, The George Washington University, Washington, DC, USA.
Rohan FernandesInstitute for Biomedical Sciences, The George Washington University, Washington, DC, USA.

Funding

Clinical and Translational Science Institute at Children's NationalUL1TR000075 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI GUAY-WOODFORD, LISA MARIE · 2012 to 2015
$13.7M
Clinical and Translational Science Institute at Children's NationalKL2TR000076 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI GUAY-WOODFORD, LISA MARIE · 2012 to 2014
$756k
NCATS NIH HHS KL2 TR000076NCATS NIH HHS UL1 TR000075
6 · The paper itself

Abstract

aimTo engineer a novel nanoimmunotherapy comprising Prussian blue nanoparticles (PBNPs) conjugated to antigen-specific cytotoxic T lymphocytes (CTL), which leverages PBNPs for their photothermal therapy (PTT) capabilities and Epstein-Barr virus (EBV) antigen-specific CTL for their ability to traffic to and destroy EBV antigen-expressing target cells. MATERIALS &

methodsPBNPs and CTL were independently biofunctionalized. Subsequently, PBNPs were conjugated onto CTL using avidin-biotin interactions. The resultant cell-nanoparticle construct (CTL:PBNPs) were analyzed for their physical, phenotypic and functional properties.

resultsBoth PBNPs and CTL maintained their intrinsic physical, phenotypic and functional properties within the CTL:PBNPs.

conclusionThis study highlights the potential of our CTL:PBNPs nanoimmunotherapy as a novel therapeutic for treating virus-associated malignancies such as EBV+ cancers.

Indexed as

Antigen-Presenting CellsCoculture TechniquesColoring AgentsEpstein-Barr Virus InfectionsFerrocyanidesHerpesvirus 4, HumanHumansImmunotherapyJurkat CellsLymphocyte ActivationNanomedicineNanoparticlesNeoplasmsPhototherapyT-Lymphocytes, CytotoxicColoring Agentsferric ferrocyanideFerrocyanidesantigen-specific T cellscell nanoparticle constructcytotoxic T lymphocyteimmunotherapynanoimmunotherapyphotothermal therapyPrussian blue nanoparticles

Identifiers

PMID27389189
PMCPMC4941545

What OpenQuestion holds

Textmetadata
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.