Evidence map›Paper›PMID 26469724›Full record

ArticleVaccine2015

Cross-stage immunity for malaria vaccine development.

Wiebke Nahrendorf, Anja Scholzen, Robert W Sauerwein, Jean Langhorne

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.6field-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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Controlled Human Malaria Infection Studies in Africa-Past, Present, and Future.Current topics in microbiology and immunology · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Functional antibodies againstWellcome open research · 2018
    Article
  13. AFrontiers in immunology · 2018
    Article
  14. Article
  15. 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

4 authors at 2 institutions in 2 countries.

Wiebke NahrendorfMill Hill Laboratory, The Francis Crick Institute, London, United Kingdom; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands. Electronic address: Wiebke.Nahrendorf@ed.ac.uk.
Anja ScholzenDepartment of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands. Electronic address: Anja.Scholzen@radboudumc.nl.
Robert W SauerweinDepartment of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands. Electronic address: Robert.Sauerwein@radboudumc.nl.
Jean LanghorneMill Hill Laboratory, The Francis Crick Institute, London, United Kingdom. Electronic address: Jean.Langhorne@crick.ac.uk.
Radboud University Medical Center · NLThe Francis Crick Institute · GB

Funding

Medical Research Council MC_U117584248Medical Research Council U117584248
6 · The paper itself

Abstract

A vaccine against malaria is urgently needed for control and eventual eradication. Different approaches are pursued to induce either sterile immunity directed against pre-erythrocytic parasites or to mimic naturally acquired immunity by controlling blood-stage parasite densities and disease severity. Pre-erythrocytic and blood-stage malaria vaccines are often seen as opposing tactics, but it is likely that they have to be combined into a multi-stage malaria vaccine to be optimally safe and effective. Since many antigenic targets are shared between liver- and blood-stage parasites, malaria vaccines have the potential to elicit cross-stage protection with immune mechanisms against both stages complementing and enhancing each other. Here we discuss evidence from pre-erythrocytic and blood-stage subunit and whole parasite vaccination approaches that show that protection against malaria is not necessarily stage-specific. Parasites arresting at late liver-stages especially, can induce powerful blood-stage immunity, and similarly exposure to blood-stage parasites can afford pre-erythrocytic immunity. The incorporation of a blood-stage component into a multi-stage malaria vaccine would hence not only combat breakthrough infections in the blood should the pre-erythrocytic component fail to induce sterile protection, but would also actively enhance the pre-erythrocytic potency of this vaccine. We therefore advocate that future studies should concentrate on the identification of cross-stage protective malaria antigens, which can empower multi-stage malaria vaccine development.

Indexed as

Cross ProtectionAntigens, ProtozoanErythrocytesLife Cycle StagesLiverMalariaMalaria VaccinesPlasmodiumVaccinationAntigens, ProtozoanMalaria VaccinesBlood-stageCross-stageImmunizationMalariaPre-erythrocyticVaccine

Identifiers

PMID26469724
PMCPMC4687527
OpenAlexW1754591538

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.