Evidence map›Paper›PMID 22311924›Full record

ArticleInfection and immunity2012

Expression, immunogenicity, histopathology, and potency of a mosquito-based malaria transmission-blocking recombinant vaccine.

D K Mathias, J L Plieskatt, J S Armistead, J M Bethony, K B Abdul-Majid, A McMillan, E Angov, M J Aryee, B Zhan, P Gillespie and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.0field-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

32 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Frontiers in immunology · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Targeting Gametocytes of the Malaria ParasitePathogens (Basel, Switzerland) · 2021
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Immune Responses to the Sexual Stages ofFrontiers in immunology · 2019
    Review
  16. Article
  17. Article
  18. Metazoan Parasite Vaccines: Present Status and Future Prospects.Frontiers in cellular and infection microbiology · 2018
    Review
  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

17 authors at 8 institutions in 1 country.

D K MathiasW. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health and Malaria Research Institute, Baltimore, Maryland, USA.
J L Plieskatt
J S Armistead
J M Bethony
K B Abdul-Majid
A McMillan
E Angov
M J Aryee
B Zhan
P Gillespie
B Keegan
A R Jariwala
W Rezende
M E Bottazzi
D G Scorpio
P J Hotez
R R Dinglasan
Johns Hopkins University · USBaylor College of Medicine · USJohns Hopkins Medicine · USTexas Children's Hospital · USWashington University Medical Center · USGeorge Washington University · USSabin Vaccine Institute · USWalter Reed Army Institute of Research · US

Funding

Institute for Clinical and Translational Research (UL1)UL1RR025005 · NCRR · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2007 to 2011
$75.8M
Training: Molecular & Cellular Bases of Infectious DiseasesT32AI007417 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Arturo Casadevall · 1994 to 2026
$11.9M
Glycobiological Analysis of Plasmodium-Vector Host InteractionsK22AI077707 · NIAID · JOHNS HOPKINS UNIVERSITY · PI DINGLASAN, RHOEL DAVID RAMOS · 2009 to 2010
$270k
NCRR NIH HHS UL1 RR 025005NCRR NIH HHS UL1 RR025005NIAID NIH HHS 1K22AI077707NIAID NIH HHS K22 AI077707
6 · The paper itself

Abstract

Vaccines have been at the forefront of global research efforts to combat malaria, yet despite several vaccine candidates, this goal has yet to be realized. A potentially effective approach to disrupting the spread of malaria is the use of transmission-blocking vaccines (TBV), which prevent the development of malarial parasites within their mosquito vector, thereby abrogating the cascade of secondary infections in humans. Since malaria is transmitted to human hosts by the bite of an obligate insect vector, mosquito species in the genus Anopheles, targeting mosquito midgut antigens that serve as ligands for Plasmodium parasites represents a promising approach to breaking the transmission cycle. The midgut-specific anopheline alanyl aminopeptidase N (AnAPN1) is highly conserved across Anopheles vectors and is a putative ligand for Plasmodium ookinete invasion. We have developed a scalable, high-yield Escherichia coli expression and purification platform for the recombinant AnAPN1 TBV antigen and report on its marked vaccine potency and immunogenicity, its capacity for eliciting transmission-blocking antibodies, and its apparent lack of immunization-associated histopathologies in a small-animal model.

Indexed as

AnimalsAnophelesAntibodiesCD13 AntigensFemaleHumansInsect VectorsMalariaMalaria VaccinesMiceMice, Inbred BALB CPlasmodium bergheiPlasmodium vivaxVaccines, SyntheticAntibodiesCD13 AntigensMalaria VaccinesVaccines, Synthetic

Identifiers

PMID22311924
PMCPMC3318422
OpenAlexW2108103857

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.