Evidence map›Paper›PMID 30361239›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2019

Single Dose of a Polyanhydride Particle-Based Vaccine Generates Potent Antigen-Specific Antitumor Immune Responses.

Emad I Wafa, Sean M Geary, Kathleen A Ross, Jonathan T Goodman, Balaji Narasimhan, Aliasger K Salem

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Self-adjuvanting cancer nanovaccines.Journal of nanobiotechnology · 2022
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Polymeric Nanoparticle-Based Vaccine Adjuvants and Delivery Vehicles.Current topics in microbiology and immunology · 2021
    Review
  8. Review
  9. Article
  10. 3D printing in drug delivery systems.Journal of 3D printing in medicine · 2019
    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 at 1 institution in 1 country.

Emad I WafaDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy (E.I.W., S.M.G., A.K.S.), University of Iowa, Iowa City, Iowa; and Department of Chemical and Biological Engineering, College of Engineering (K.A.R., J.T.G., B.N.) and Nanovaccine Institute (K.A.R., B.N., A.K.S.), Iowa State University, Ames, Iowa.
Sean M GearyDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy (E.I.W., S.M.G., A.K.S.), University of Iowa, Iowa City, Iowa; and Department of Chemical and Biological Engineering, College of Engineering (K.A.R., J.T.G., B.N.) and Nanovaccine Institute (K.A.R., B.N., A.K.S.), Iowa State University, Ames, Iowa.
Kathleen A RossDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy (E.I.W., S.M.G., A.K.S.), University of Iowa, Iowa City, Iowa; and Department of Chemical and Biological Engineering, College of Engineering (K.A.R., J.T.G., B.N.) and Nanovaccine Institute (K.A.R., B.N., A.K.S.), Iowa State University, Ames, Iowa.
Jonathan T GoodmanDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy (E.I.W., S.M.G., A.K.S.), University of Iowa, Iowa City, Iowa; and Department of Chemical and Biological Engineering, College of Engineering (K.A.R., J.T.G., B.N.) and Nanovaccine Institute (K.A.R., B.N., A.K.S.), Iowa State University, Ames, Iowa.
Balaji NarasimhanDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy (E.I.W., S.M.G., A.K.S.), University of Iowa, Iowa City, Iowa; and Department of Chemical and Biological Engineering, College of Engineering (K.A.R., J.T.G., B.N.) and Nanovaccine Institute (K.A.R., B.N., A.K.S.), Iowa State University, Ames, Iowa.
Aliasger K SalemDepartment of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy (E.I.W., S.M.G., A.K.S.), University of Iowa, Iowa City, Iowa; and Department of Chemical and Biological Engineering, College of Engineering (K.A.R., J.T.G., B.N.) and Nanovaccine Institute (K.A.R., B.N., A.K.S.), Iowa State University, Ames, Iowa aliasger-salem@uiowa.edu.ORCID 0000-0002-1923-6633
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
Nanovaccine platforms to combat pancreatic cancerU01CA213862 · NCI · IOWA STATE UNIVERSITY · PI JAIN, MANEESH, NARASIMHAN, BALAJI · 2017 to 2021
$2.7M
NCI NIH HHS P30 CA086862NCI NIH HHS U01 CA213862NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Many factors affect vaccine efficacy. One of the most salient is the frequency and intervals of vaccine administration. In this study, we assessed the vaccine administration modality for a recently reported polyanhydride-based vaccine formulation, shown to generate antitumor activity. Polyanhydride particles encapsulating ovalbumin (OVA) were prepared using a double-emulsion technique and subcutaneously delivered to mice either as a single-dose or as prime-boost vaccine regimens in which two different time intervals between prime and boost were assessed (7 or 21 days). This was followed by measurement of cellular and humoral immune responses, and subsequent challenge of the mice with a lethal dose of E.G7-OVA cells to evaluate tumor protection. Interestingly, a single dose of the polyanhydride particle-based formulation induced sustained OVA-specific cellular immune responses just as effectively as the prime-boost regimens. In addition, mice receiving single-dose vaccine had similar levels of protection against tumor challenge compared with mice administered prime-boosts. In contrast, measurements of OVA-specific IgG antibody titers indicated that a booster dose was required to stimulate strong humoral immune responses, since it was observed that mice administered a prime-boost vaccine had significantly higher OVA-specific IgG

Indexed as

PolyanhydridesAnimalsCancer VaccinesDrug CompoundingExcipientsFemaleImmunity, CellularImmunity, HumoralImmunization, SecondaryImmunoglobulin GMiceMice, Inbred C57BLNanoparticlesNeoplasms, ExperimentalOvalbuminSuspensionsCancer VaccinesExcipientsImmunoglobulin GOvalbuminPolyanhydridesSuspensions

Identifiers

PMID30361239
PMCPMC6806631
OpenAlexW2898454512

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.