Evidence map›Paper›PMID 30419362›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2019

Intratumoral delivery of antigen with complement C3-bound liposomes reduces tumor growth in mice.

Alexandra Francian, Shelby Namen, Madigan Stanley, Kristine Mann, Holly Martinson, Max Kullberg

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Drug delivery methods for cancer immunotherapy.Drug delivery and translational research · 2024
    Review
  8. Article
  9. Article
  10. Overcoming physical stromal barriers to cancer immunotherapy.Drug delivery and translational research · 2021
    Review
  11. Review
  12. Article
  13. Using nanoparticles forInternational journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2020
    Article
  14. Complement System: a Neglected Pathway in Immunotherapy.Clinical reviews in allergy & immunology · 2020
    Review
  15. Review
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 1 institution in 1 country.

Alexandra FrancianWWAMI Medical Education Program, University of Alaska Anchorage, Anchorage, AK, USA.
Shelby NamenWWAMI Medical Education Program, University of Alaska Anchorage, Anchorage, AK, USA.
Madigan StanleyWWAMI Medical Education Program, University of Alaska Anchorage, Anchorage, AK, USA.
Kristine MannWWAMI Medical Education Program, University of Alaska Anchorage, Anchorage, AK, USA.
Holly MartinsonWWAMI Medical Education Program, University of Alaska Anchorage, Anchorage, AK, USA.
Max KullbergWWAMI Medical Education Program, University of Alaska Anchorage, Anchorage, AK, USA. Electronic address: mpkullberg@alaska.edu.
University of Alaska Anchorage · US

Funding

The Administrative CoreP20GM103395 · NIGMS · UNIVERSITY OF ALASKA FAIRBANKS · PI BRIAN M BARNES · 2012 to 2026
$66.1M
Enhancing Tumor Antigen Presentation with Complement Targeted NanoparticlesR15CA227740 · NCI · UNIVERSITY OF ALASKA ANCHORAGE · PI KULLBERG, MAX PETER, MARTINSON, HOLLY A · 2018 to 2022
$937k
NCI NIH HHS R15 CA227740NIGMS NIH HHS P20 GM103395
6 · The paper itself

Abstract

Antigen presenting cells (APCs) initiate the immune response against cancer by engulfing and presenting tumor antigens to T cells. Our lab has recently developed a liposomal nanoparticle that binds complement C3 proteins, allowing it to bind to the complement C3 receptors of APCs and directly deliver antigenic peptides. APCs were shown to internalize and process complement C3-bound liposomes containing ovalbumin (OVA), resulting in a significant increase in activated T cells that recognize OVA. Mice bearing A20-OVA lymphoma tumors were treated with OVA-loaded C3-liposomes, which led to reduced tumor growth in both treated and distal tumors in all mice. Peripheral blood from treated mice had a lower percentage of immunosuppressive myeloid derived suppressor cells (MDSCs), a higher percentage of B cells, and increased anti-OVA IgG

Indexed as

AnimalsAntigen-Presenting CellsCell Line, TumorCell ProliferationComplement C3Dendritic CellsEndocytosisHumansImmunoglobulin GLiposomesLiverLymphocyte ActivationMaleMice, Inbred BALB CMice, Inbred C57BLMyeloid-Derived Suppressor CellsComplement C3Immunoglobulin GLiposomesOvalbuminAntigen-presenting cellsCancer immunotherapyComplement C3NanoparticleTargeted deliveryTumor antigen

Identifiers

PMID30419362
PMCPMC6509024
OpenAlexW2900004110

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.