Evidence map›Paper›PMID 15501757›Full record

Trial reportInfection and immunity2004

Strain-specific humoral response to a polymorphic malaria vaccine.

Christian Flück, Tom Smith, Hans-Peter Beck, Andrea Irion, Inoni Betuela, Michael P Alpers, Robin Anders, Allan Saul, Blaise Genton, Ingrid Felger

Open access · greenAbstract readClinical TrialClinical Trial, Phase IClinical Trial, Phase II
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 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Vaccines for preventing malaria (blood-stage).The Cochrane database of systematic reviews · 2006
    Pooled it
  2. Allelic frequency ofMalariaWorld journal · 2025
    Article
  3. Naturally acquired IgG responses toFrontiers in immunology · 2024
    Article
  4. Article
  5. Review
  6. Host-Malaria Parasite Interactions and Impacts on Mutual Evolution.Frontiers in cellular and infection microbiology · 2020
    Review
  7. Article
  8. Article
  9. Disordered epitopes as peptide vaccines.Peptide science (Hoboken, N.J.) · 2018
    Review
  10. Higher Complexity of Infection and Genetic Diversity ofThe American journal of tropical medicine and hygiene · 2017
    Article
  11. Review
  12. Regulating STING in health and disease.Journal of inflammation (London, England) · 2017
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

10 authors at 5 institutions in 4 countries.

Christian FlückSwiss Tropical Institute, Socinstrasse 57, Basel.
Tom Smith
Hans-Peter Beck
Andrea Irion
Inoni Betuela
Michael P Alpers
Robin Anders
Allan Saul
Blaise Genton
Ingrid Felger
Swiss Tropical and Public Health Institute · CHCurtin University · AULa Trobe University · AUNational Institutes of Health · USPapua New Guinea Institute of Medical Research · PG

Funding

RECOMBINANT PROTEIN EXPRESSION UNIT (RPEU)Z01AI000727 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI SAUL, ALLAN · 1995 to 2006
–
6 · The paper itself

Abstract

The 3D7 form of the merozoite surface protein 2 (MSP2) of Plasmodium falciparum was one of three subunits of the malaria vaccine Combination B that were tested in a phase I/IIb double-blind randomized placebo-controlled trial, which was undertaken with 120 Papua New Guinean children of 5 to 9 years of age. Because only one variant of the highly polymorphic MSP2 was used for vaccination, we examined whether the elicited response was directed against conserved or strain-specific epitopes. Postvaccination (week 12) titers of antibody against recombinantly expressed individual domains of MSP2 were measured by enzyme-linked immunosorbent assay and compared to baseline values. We found that vaccination with the 3D7 form of MSP2 induced a significant strain-specific humoral response directed against the repetitive and semiconserved family-specific part. The conserved N- and C-terminal domains were not immunogenic. Titers of antibody against the alternate FC27 family-specific domain showed a tendency to increase in vaccinated children, but there was no increase in antibodies against FC27-type 32-mer repeats. These results indicate that vaccination with one MSP2 variant mainly induced a strain-specific response, which can explain the selective effect of vaccination with combination B on the genotypes of breakthrough parasites. These findings support the inclusion of both family-specific domains (3D7 and FC27) in an improved vaccine formulation.

Indexed as

Polymorphism, GeneticAmino Acid SequenceAnimalsAntibodies, ProtozoanAntigens, ProtozoanChildChild, PreschoolDouble-Blind MethodHumansMalaria, FalciparumMalaria VaccinesNew GuineaPeptidesPlasmodium falciparumProtozoan ProteinsRecombinant ProteinsAntibodies, ProtozoanAntigens, ProtozoanMalaria Vaccinesmerozoite surface protein 2, PlasmodiumPeptidesProtozoan ProteinsRecombinant Proteins

Identifiers

PMID15501757
PMCPMC523016
OpenAlexW2100533040

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.