Evidence map›Paper›PMID 20713623›Full record

ArticleInfection and immunity2010

New candidate vaccines against blood-stage Plasmodium falciparum malaria: prime-boost immunization regimens incorporating human and simian adenoviral vectors and poxviral vectors expressing an optimized antigen based on merozoite surface protein 1.

Anna L Goodman, C Epp, D Moss, A A Holder, J M Wilson, G P Gao, C A Long, E J Remarque, A W Thomas, V Ammendola and 8 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
9.4field-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.

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

34 citing papers in PubMed, 47 citations in OpenAlex.

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  16. Neutralization of Plasmodium falciparum merozoites by antibodies against PfRH5.Journal of immunology (Baltimore, Md. : 1950) · 2014
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

18 authors at 7 institutions in 4 countries.

Anna L GoodmanThe Jenner Institute, University of Oxford, Oxford, United Kingdom. anna.goodman@nhs.net
C Epp
D Moss
A A Holder
J M Wilson
G P Gao
C A Long
E J Remarque
A W Thomas
V Ammendola
S Colloca
M D J Dicks
S Biswas
D Seibel
L M van Duivenvoorde
S C Gilbert
A V S Hill
S J Draper
Biomedical Primate Research Centre · NLJenner Institute · GBUniversity of Oxford · GBUniversity Hospital Heidelberg · DENational Institutes of Health · USTranslational Therapeutics (United States) · USUniversity of Pennsylvania · US

Funding

Vector CoreP30DK047757 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI WILSON, JAMES M · 1993 to 2017
$18.0M
Host Immune Responses to Antigens of Malaria ParasitesZIAAI001020 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LONG, CAROLE · 2009 to 2025
$13.6M
Intramural NIH HHSMedical Research Council G0600424Medical Research Council G0700735Medical Research Council G1000527Medical Research Council G1000527(95710)Medical Research Council MC_U117532067NIDDK NIH HHS P30 DK047757NIDDK NIH HHS P30 DK-47757Wellcome Trust
6 · The paper itself

Abstract

Although merozoite surface protein 1 (MSP-1) is a leading candidate vaccine antigen for blood-stage malaria, its efficacy in clinical trials has been limited in part by antigenic polymorphism and potentially by the inability of protein-in-adjuvant vaccines to induce strong cellular immunity. Here we report the design of novel vectored Plasmodium falciparum vaccines capable of overcoming such limitations. We optimized an antigenic insert comprising the four conserved blocks of MSP-1 fused to tandemly arranged sequences that represent both allelic forms of the dimorphic 42-kDa C-terminal region. Inserts were expressed by adenoviral and poxviral vectors and employed in heterologous prime-boost regimens. Simian adenoviral vectors were used in an effort to circumvent preexisting immunity to human adenoviruses. In preclinical studies these vaccines induced potent cellular immune responses and high-titer antibodies directed against MSP-1. The antibodies induced were found to have growth-inhibitory activity against dimorphic allelic families of P. falciparum. These vectored vaccines should allow assessment in humans of the safety and efficacy of inducing strong cellular as well as cross-strain humoral immunity to P. falciparum MSP-1.

Indexed as

Genetic VectorsMalaria VaccinesAdenoviruses, HumanAdenoviruses, SimianAnimalsAntibodies, ProtozoanChick EmbryoDNA VirusesDrug DesignErythrocytesFemaleHumansImmunizationImmunization, SecondaryMalaria, FalciparumMerozoite Surface Protein 1Antibodies, ProtozoanMalaria VaccinesMerozoite Surface Protein 1

Identifiers

PMID20713623
PMCPMC2976338
OpenAlexW2164379046

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.