Evidence map›Paper›PMID 19464533›Full record

ArticleVaccine2009

The mast cell activator compound 48/80 is safe and effective when used as an adjuvant for intradermal immunization with Bacillus anthracis protective antigen.

Afton L McGowen, Laura P Hale, Christopher P Shelburne, Soman N Abraham, Herman F Staats

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 82 citations in OpenAlex.

  1. Broadly active intranasal influenza vaccine with a nanocomplex particulate adjuvant targeting mast cells and toll-like receptor 9.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  2. Article
  3. Mast cell activators as adjuvants for intranasal mucosal vaccines.International journal of pharmaceutics · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Angiogenic Host Defense Peptide AG-30/5C and Bradykinin BJournal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  12. Article
  13. Mast cell activators as novel immune regulators.Current opinion in pharmacology · 2018
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Inducing Mucosal IgA: A Challenge for Vaccine Adjuvants and Delivery Systems.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Review
  19. Article
  20. 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 3 institutions in 1 country.

Afton L McGowenDepartment of Pathology, Duke University Medical Center, Durham, NC 27710, USA.
Laura P Hale
Christopher P Shelburne
Soman N Abraham
Herman F Staats
Duke Medical Center · USDuke University Hospital · USDuke University · US

Funding

Mast Cell Activator as Adjuvant for Biodefense VaccinesR21AI059591 · NIAID · DUKE UNIVERSITY · PI STAATS, HERMAN F. · 2005 to 2006
$609k
NIAID NIH HHS R21 AI-059591NIAID NIH HHS R21 AI059591
6 · The paper itself

Abstract

We evaluated the safety and efficacy of the mast cell activator compound 48/80 (C48/80) when used as an adjuvant delivered intradermally (ID) with recombinant anthrax protective antigen (rPA) in comparison with two well-known adjuvants. Mice were vaccinated in the ear pinnae with rPA or rPA+C48/80, CpG oligodeoxynucleotides (CpG), or cholera toxin (CT). All adjuvants induced similar increases in serum anti-rPA IgG and lethal toxin neutralizing antibodies. C48/80 induced a balanced cytokine production (Th1/Th2/Th17) by antigen-restimulated splenocytes, minimal injection site inflammation, and no antigen-specific IgE. Histological analysis demonstrated that vaccination with C48/80 reduced the number of resident mast cells and induced an injection site neutrophil influx within 24h. Our data demonstrate that C48/80 is a safe and effective adjuvant, when used by the intradermal route, to induce protective antibody and balanced Th1/Th2/Th17 responses.

Indexed as

Adjuvants, ImmunologicAdministration, CutaneousAnimalsAnthrax VaccinesAntibodies, BacterialAntigens, BacterialBacterial ToxinsCytokinesFemaleImmunizationImmunoglobulin EMast CellsMiceMice, Inbred C3Hp-Methoxy-N-methylphenethylamineAdjuvants, Immunologicanthrax toxinAnthrax VaccinesAntibodies, BacterialAntigens, BacterialBacterial ToxinsCytokinesImmunoglobulin Ep-Methoxy-N-methylphenethylamine

Identifiers

PMID19464533
PMCPMC2743390
OpenAlexW2088919776

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.