Evidence map›Paper›PMID 24115675›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2014

In vivo immune cell distribution of gold nanoparticles in naïve and tumor bearing mice.

Joao Paulo Mattos Almeida, Adam Yuh Lin, Robert James Langsner, Phillip Eckels, Aaron Edward Foster, Rebekah Anna Drezek

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Current role of nanoparticles in the treatment of lung cancer.Journal of clinical and translational research · 2021
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Stromal barriers and strategies for the delivery of nanomedicine to desmoplastic tumors.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  20. 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.

Joao Paulo Mattos AlmeidaDepartment of Bioengineering, Rice University, Houston, TX, USA, 77030.
Adam Yuh Lin
Robert James Langsner
Phillip Eckels
Aaron Edward Foster
Rebekah Anna Drezek

Funding

Nanobiology Interdisciplinary Graduate Training ProgramT32EB009379 · NIBIB · RICE UNIVERSITY · PI DREZEK, REBEKAH A. · 2009 to 2013
$1.6M
CpG-ODN Coated Hollow Gold Nanoshells for Photothermal TherapyR01CA172836 · NCI · BELLICUM PHARMACEUTICALS, INC. · PI FOSTER, AARON E. · 2013 to 2016
$1.4M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA172836NCI NIH HHS R01CA172836NIBIB NIH HHS T32 EB009379NIBIB NIH HHS T32EB009379
6 · The paper itself

Abstract

Gold nanoparticles (AuNP) have been widely used for drug delivery and have recently been explored for applications in cancer immunotherapy. Although AuNPs are known to accumulate heavily in the spleen, the particle distribution within immune cells has not been thoroughly studied. Here, cellular distribution of Cy5 labeled 50 nm AuNPs is characterized within the immune populations of the spleen from naïve and tumor bearing mice using flow cytometry. Surprisingly, approximately 30% of the detected AuNPs are taken up by B cells at 24 h, with about 10% in granulocytes, 18% in dendritic cells, and 8% in T cells. In addition, 3% of the particles are detected within myeloid derived suppressor cells, an immune suppressive population that could be targeted for cancer immunotherapy. Furthermore, it is observed that, over time, the particles traveled from the red pulp and marginal zone to the follicles of the spleen. Taking into consideration that the particle cellular distribution does not change at 1, 6 and 24 h, it is highly suggestive that the immune populations carry the particles and migrate through the spleen instead of the particles migrating through the tissue by cell-cell transfer. Finally, no difference is observed in particle distribution between naïve and tumor bearing mice in the spleen, and nanoparticles are detected within 0.7% of dendritic cells of the tumor microenvironment. Overall, these results can help inform and influence future AuNP delivery design criteria including future applications for nanoparticle-mediated immunotherapy.

Indexed as

AnimalsB-LymphocytesCD11c AntigenFlow CytometryGoldInjections, IntravenousLeukocytesMelanoma, ExperimentalMetal NanoparticlesMice, Inbred C57BLSpleenTumor MicroenvironmentCD11c AntigenGoldbiodistributioncancergold nanoparticlesimmune systemimmunotherapyspleen

Identifiers

PMID24115675
PMCPMC3962812

What OpenQuestion holds

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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.