Evidence map›Paper›PMID 15501783›Full record

Trial reportInfection and immunity2004

Phase I testing of a malaria vaccine composed of hepatitis B virus core particles expressing Plasmodium falciparum circumsporozoite epitopes.

Elizabeth H Nardin, Giane A Oliveira, J Mauricio Calvo-Calle, Kristiane Wetzel, Carolin Maier, Ashley J Birkett, Pramod Sarpotdar, Michael L Corado, George B Thornton, Annette Schmidt

Abstract readClinical TrialClinical Trial, Phase IControlled Clinical Trial
In one paragraph

Trial report in Infection and immunity, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Emerging concepts in the science of vaccine adjuvants.Nature reviews. Drug discovery · 2021
    Review
  17. Review
  18. Article
  19. Synthesis and Assembly of Hepatitis B Virus-Like Particles in aFrontiers in bioengineering and biotechnology · 2020
    Article
  20. NPJ vaccines · 2017
    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

10 authors at 1 institution in 1 country.

Elizabeth H NardinNew York University School of Medicine, Department of Medical and Molecular Parasitology, 341 East 25th St., New York, NY 10010, USA. nardie01@med.nyu.edu
Giane A Oliveira
J Mauricio Calvo-Calle
Kristiane Wetzel
Carolin Maier
Ashley J Birkett
Pramod Sarpotdar
Michael L Corado
George B Thornton
Annette Schmidt
New York University · US

Funding

IMMUNOGENICITY OF SYNTHETIC POLYOXIME MALARIA VACCINESR01AI045138 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NARDIN, ELIZABETH H · 1999 to 2009
$3.5M
NIAID NIH HHS R01 AI045138
6 · The paper itself

Abstract

We report the first phase I trial to assess the safety and immunogenicity of a malaria vaccine candidate, ICC-1132 (Malarivax), composed of a modified hepatitis B virus core protein (HBc) containing minimal epitopes of the Plasmodium falciparum circumsporozoite (CS) protein. When expressed in Escherichia coli, the recombinant ICC-1132 protein forms virus-like particles that were found to be highly immunogenic in preclinical studies of mice and monkeys. Twenty healthy adult volunteers received a 20- or a 50-microg dose of alum-adsorbed ICC-1132 administered intramuscularly at 0, 2, and 6 months. The majority of volunteers in the group receiving the 50-microg dose developed antibodies to CS repeats as well as to HBc. Malaria-specific T cells that secreted gamma interferon were also detected after a single immunization with ICC-1132-alum. These studies support ICC-1132 as a promising malaria vaccine candidate for further clinical testing using more-potent adjuvant formulations and confirm the potential of modified HBc virus-like particles as a delivery platform for vaccines against other human pathogens.

Indexed as

AdolescentAdultAlum CompoundsAmino Acid SequenceAnimalsAntibodies, ProtozoanDouble-Blind MethodEpitopesHepatitis BHepatitis B Core AntigensHumansInterferon-gammaMalaria, FalciparumMalaria VaccinesMiddle AgedMolecular Sequence DataAlum Compoundsaluminum sulfateAntibodies, Protozoancircumsporozoite protein, ProtozoanEpitopesHepatitis B Core AntigensInterferon-gammaMalaria VaccinesProtozoan ProteinsVaccines, Synthetic

Identifiers

PMID15501783
PMCPMC523031
OpenAlexW2138147357

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.