Evidence map›Paper›PMID 16914237›Full record

ReviewVaccine2007

Viral vectors for malaria vaccine development.

Shengqiang Li, Emily Locke, Joseph Bruder, David Clarke, Denise L Doolan, Menzo J E Havenga, Adrian V S Hill, Peter Liljestrom, Thomas P Monath, Hussein Y Naim and 6 more

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Vaccine, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00392015 (A Two Part Clinical Trial Assessing the Safety, Tolerability, Immunogenicity and Protective Efficacy of NMRC-M3V-Ad-PfCA, a Multivalent, Adenovirus-Vectored Plasmodium Falciparum Malaria Vaccine, in Healthy, Malaria-Naïve Adults), which is not on this map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
10.0field-weighted citation impact, top 2% 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.

NCT00392015 phase1 / phase2completednot on this map

A Two Part Clinical Trial Assessing the Safety, Tolerability, Immunogenicity and Protective Efficacy of NMRC-M3V-Ad-PfCA, a Multivalent, Adenovirus-Vectored Plasmodium Falciparum Malaria Vaccine, in Healthy, Malaria-Naïve Adults

TypeinterventionalSponsorU.S. Army Medical Research and Development CommandRan2006 to 2017Enrolled59ConditionsPlasmodium FalciparumArmsNMRC-M3V-Ad-PfCA, NMRC-MV-Ad-PfC, NMRC-M3V-Ad-PfCA
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 72 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. A landscape review of malaria vaccine candidates in the pipeline.Tropical diseases, travel medicine and vaccines · 2024
    Review
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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

16 authors at 10 institutions in 5 countries.

Shengqiang LiPATH Malaria Vaccine Initiative, Bethesda, MD, USA. sheng.li@hhs.gov
Emily Locke
Joseph Bruder
David Clarke
Denise L Doolan
Menzo J E Havenga
Adrian V S Hill
Peter Liljestrom
Thomas P Monath
Hussein Y Naim
Christian Ockenhouse
De-chu C Tang
Kent R Van Kampen
Jean-Francois Viret
Fidel Zavala
Filip Dubovsky
U.S. President's Malaria Initiative · USCemex (Switzerland) · CHAbcam (United States) · USGenVec · USJohns Hopkins University · USJohnson & Johnson (Netherlands) · NLKarolinska Institutet · SENaval Medical Research Command · USUniversity of Oxford · GBWalter Reed Army Institute of Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A workshop on viral vectors for malaria vaccine development, organized by the PATH Malaria Vaccine Initiative, was held in Bethesda, MD on October 20, 2005. Recent advancements in viral-vectored malaria vaccine development and emerging vector technologies were presented and discussed. Classic viral vectors such as poxvirus, adenovirus and alphavirus vectors have been successfully used to deliver malaria antigens. Some of the vaccine candidates have demonstrated their potential in inducing malaria-specific immunity in animal models and human trials. In addition, emerging viral-vector technologies, such as measles virus (MV), vesicular stomatitis virus (VSV) and yellow fever (YF) virus, may also be useful for malaria vaccine development. Studies in animal models suggest that each viral vector is unique in its ability to induce humoral and/or cellular immune responses. Those studies have also revealed that optimization of Plasmodium genes for mammalian expression is an important aspect of vaccine design. Codon-optimization, surface-trafficking, de-glycosylation and removal of toxic domains can lead to improved immunogenicity. Understanding the vector's ability to induce an immune response and the expression of malaria antigens in mammalian cells will be critical in designing the next generation of viral-vectored malaria vaccines.

Indexed as

AdenoviridaeAlphavirusGenetic VectorsMalaria VaccinesMeasles virusPoxviridaeVaccines, SyntheticVesicular stomatitis Indiana virusVirusesYellow fever virusMalaria VaccinesVaccines, Synthetic

Identifiers

PMID16914237
PMCPMC7131149
OpenAlexW1989422723

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.