Evidence map›Paper›PMID 23716612›Full record

ArticleInfection and immunity2013

Development of a chimeric Plasmodium berghei strain expressing the repeat region of the P. vivax circumsporozoite protein for in vivo evaluation of vaccine efficacy.

Diego A Espinosa, Anjali Yadava, Evelina Angov, Paul L Maurizio, Christian F Ockenhouse, Fidel Zavala

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2013. 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
4.6field-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

39 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Plasmodium circumsporozoite protein.Trends in parasitology · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Generation of a Genetically Modified ChimericFrontiers in cellular and infection microbiology · 2020
    Article
  17. Article
  18. Article
  19. Review
  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

6 authors at 2 institutions in 1 country.

Diego A EspinosaJohns Hopkins Malaria Research Institute and Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA.
Anjali Yadava
Evelina Angov
Paul L Maurizio
Christian F Ockenhouse
Fidel Zavala
Johns Hopkins University · USWalter Reed Army Institute of Research · US

Funding

EFFECTOR AND MEMORY ANTIMALARIA CD8+ CELL RESPONSESR01AI044375 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ZAVALA, FIDEL P · 1999 to 2013
$6.5M
EFFECTOR AND MEMORY ANTIMALARIA CD8+ T CELL RESPONSESR21AI044375 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ZAVALA, FIDEL P · 1999 to 1999
–
NIAID NIH HHS AI44375NIAID NIH HHS R01 AI044375NIAID NIH HHS R21 AI044375
6 · The paper itself

Abstract

The development of vaccine candidates against Plasmodium vivax-the most geographically widespread human malaria species-is challenged by technical difficulties, such as the lack of in vitro culture systems and availability of animal models. Chimeric rodent Plasmodium parasites are safe and useful tools for the preclinical evaluation of new vaccine formulations. We report the successful development and characterization of chimeric Plasmodium berghei parasites bearing the type I repeat region of P. vivax circumsporozoite protein (CSP). The P. berghei-P. vivax chimeric strain develops normally in mosquitoes and produces highly infectious sporozoites that produce patent infection in mice that are exposed to the bites of as few as 3 P. berghei-P. vivax-infected mosquitoes. Using this transgenic parasite, we demonstrate that monoclonal and polyclonal antibodies against P. vivax CSP strongly inhibit parasite infection and thus support the notion that these antibodies play an important role in protective immunity. The chimeric parasites we developed represent a robust model for evaluating protective immune responses against P. vivax vaccines based on CSP.

Indexed as

AnimalsAntibodies, ProtozoanAntigens, ProtozoanChimeraFluorescent Antibody Technique, IndirectMalaria VaccinesMicePlasmodium bergheiPlasmodium vivaxProtozoan ProteinsReverse Transcriptase Polymerase Chain ReactionTransfectionAntibodies, ProtozoanAntigens, Protozoancircumsporozoite protein, ProtozoanMalaria VaccinesProtozoan Proteins

Identifiers

PMID23716612
PMCPMC3719583
OpenAlexW2100733023

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.