Evidence map›Paper›PMID 23153760›Full record

ArticleActa biomaterialia2013

Characterizing the antitumor response in mice treated with antigen-loaded polyanhydride microparticles.

Vijaya B Joshi, Sean M Geary, Brenda R Carrillo-Conde, Balaji Narasimhan, Aliasger K Salem

Abstract read
In one paragraph

Article in Acta biomaterialia, 2013. 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
1.0field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Polyanhydride nanoparticles stabilize pancreatic cancer antigen MUC4β.Journal of biomedical materials research. Part A · 2021
    Article
  5. Article
  6. Article
  7. Biodegradable polymers for modern vaccine development.Journal of industrial and engineering chemistry (Seoul, Korea) · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Nano-enabled delivery of diverse payloads across complex biological barriers.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  17. Nanoparticles in vaccine delivery.The AAPS journal · 2015
    Article
  18. Review
  19. 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

5 authors at 2 institutions in 1 country.

Vijaya B JoshiDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 52242, USA.
Sean M Geary
Brenda R Carrillo-Conde
Balaji Narasimhan
Aliasger K Salem
University of Iowa · USIowa State University · US

Funding

The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI HOUTMAN, JON C.D. · 2002 to 2021
$45.7M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI HANS-JOACHIM LEHMLER · 1990 to 2026
$40.5M
Chitosan-plasmid DNA nanoplexes and adenoviruses as prostate cancer vaccinesR21CA133456 · NCI · UNIVERSITY OF IOWA · PI SALEM, ALIASGER K · 2008 to 2009
$338k
Engineered Optimal Adjuvant and Antigen Release from Biodegradable NanoparticlesR21CA128414 · NCI · UNIVERSITY OF IOWA · PI SALEM, ALIASGER K · 2009 to 2010
$264k
NCI NIH HHS 1R21CA128414-01A2NCI NIH HHS P50 CA097274NCI NIH HHS R21 CA128414NCI NIH HHS R21 CA133456NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Delivery of vaccine antigens with an appropriate adjuvant can trigger potential immune responses against cancer leading to reduced tumor growth and improved survival. In this study, various formulations of a bioerodible amphiphilic polyanhydride copolymer based on 1,8-bis(p-carboxyphenoxy)-3,6-dioxaoctane (CPTEG) and 1,6-bis(p-carboxyphenoxy) hexane (CPH) with inherent adjuvant properties were evaluated for antigen-loading properties, immunogenicity and antitumor activity. Mice were vaccinated with 50:50 CPTEG:CPH microparticles encapsulating a model tumor antigen, ovalbumin (OVA), in combination with the Toll-like receptor-9 agonist, CpG oligonucleotide 1826 (CpG ODN). Mice treated with OVA-encapsulated CPTEG:CPH particles elicited the highest CD8(+) T cell responses on days 14 and 20 when compared to other treatment groups. This treatment group also displayed the most delayed tumor progression and the most extended survival times. Particles encapsulating OVA and CpG ODN generated the highest anti-OVA IgG(1) antibody responses in mice but these mice did not show significant tumor protection. These results suggest that antigen-loaded CPTEG:CPH microparticles can stimulate antigen-specific cellular responses and could therefore potentially be used to promote antitumor responses in cancer patients.

Indexed as

AnimalsAntibody SpecificityAntigensAntineoplastic AgentsImmunoglobulin GMaleMiceMice, Inbred C57BLNanoparticlesNeoplasmsOligodeoxyribonucleotidesOvalbuminParticle SizePolyanhydridesPolyethylene GlycolsStatic ElectricityAntigensAntineoplastic AgentsCPG-oligonucleotideImmunoglobulin GOligodeoxyribonucleotidesOvalbuminpoly(1,6-bis-4-carboxyphenoxyhexane)poly(1,8-bis(4-carboxyphenoxy)-3,6-dioxaoctane)PolyanhydridesPolyethylene Glycols

Identifiers

PMID23153760
PMCPMC3562412
OpenAlexW2012354594

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.