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vaccines

Special Report: Development of vaccines to prevent malaria in pregnant women: WHO MALVAC meeting report

Author(s): 
Clara Menéndez, Vasee S Moorthy, Zarifah Reed, Azucena Bardají, Pedro Alonso and Graham V Brown
Reference: 
Expert Review of Vaccines,September 2011, Vol. 10, No. 9, Pages 1271-1280
Contact email: 
vmoorthy@malariavaccine.org

This report includes brief summaries of what is known, and major knowledge gaps in disease burden estimation, pathogenesis and immunity, and the challenges with current preventive strategies for malaria in pregnancy.

Opinion: Uses of mosquito-stage transmission-blocking vaccines against Plasmodium falciparum

Author(s): 
Thomas A. Smith, Nakul Chitnis, Olivier J.T. Briët, Marcel Tanner
Reference: 
Trends in Parasitology, Volume 27, Issue 5, May 2011, Pages 190-196
Contact email: 
Thomas-A.Smith@unibas.ch

A quantitative framework is used to explore the potential applications and probable effects of sexual stage or mosquito stage transmission blocking vaccines (TBVs) against malaria.

Open Access | Oral Presentation: Predicted impact of mosquito-stage transmission-blocking vaccines using an ensemble of microsimulations

Author(s): 
Aurelio Di Pasquale, Nicolas Maire, Thomas Smith
Reference: 
Malaria Journal 2010, 9(Suppl 2):O11 (20 October 2010)

The outputs of the stochastic individual-based simulations are predictions of the epidemiological impact and comparative cost-effectiveness of conceivable control measures, alone or in combination.

Microbial Immunity and Vaccines: 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 Me

Author(s): 
Anna L.,C. Epp., et al
Reference: 
Infect. Immun., Nov 2010; 78: 4601 - 4612.
Contact email: 
anna.goodman@nhs.net

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.

CLOSED: The Second International Conference, Malaria Vaccines for the World

Date: 28-30 September 2010
Venue: Kellogg Conference Hotel Gallaudet University, Washington DC, USA

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Open Access | WHO policy development processes for a new vaccine: case study of malaria vaccines

Author(s): 
Milstien J, Cardenas V, Cheyne J, Brooks A
Reference: 
Malaria Journal 2010, 9:182 (24 June 2010)

Although policy issues may be more complex for future vaccines, the lead-time between the date of product regulatory approval and a recommendation for its use in developing countries is decreasing.

Differential effects of C3d on the immunogenicity of gene gun vaccines encoding Plasmodium falciparum and Plasmodium berghei MSP142

Author(s): 
Richard Weiss, Maximilian Gabler, Thomas Jacobs, Tim-Wolf Gilberger, Josef Thalhamer, Sandra Scheiblhofer
Reference: 
Vaccine, Volume 28, Issue 28, 17 June 2010, Pages 4515-4522

In this work, C3d exerted differential effects on humoral immune responses after gene gun immunization of mice with plasmids encoding the malaria blood stage antigen MSP142 depending on the nature of the protein Plasmodium falciparum vs. Plasmodium berghei MSP), the localization of the C3d moiety (C-terminal vs. N-terminal), and the presence of putative N-glycosylation sites.

Evaluation of the safety and immunogenicity of Plasmodium falciparum apical membrane antigen 1, merozoite surface protein 1 or RTS,S vaccines with adjuvant system AS02A administered alone or concurrently in rhesus monkeys

Author(s): 
Pichyangkul S., Kum-Arb U., et al.
Reference: 
Vaccine, Volume 28, Issue 2, 11 December 2009, Pages 452-462
Contact email: 
SathitP@afrims.org

The objectives of this study were (i) to determine whether MSP142 and AMA1 vaccines formulated with the AS02A Adjuvant System were safe and immunogenic in the rhesus monkey model; (ii) to investigate whether MSP142 or AMA1 induced immune interference to each other, or to RTS,S, when added singly or in combinations at a single injection site; (iii) in the event of immune interference, to determine if this could be reduced when antigens were administered at separate sites.

Special Focus Review: Molecular vaccines for malaria

Author(s): 
Joseph T. Bruder, Evelina Ango, Keith J. Limbach and Thomas L. Richie
Reference: 
Human Vaccines, Volume 6, Issue 1 January 2010 Pages 54 - 77
Contact email: 
jbruder@genvec.com

In this review, we discuss the molecular aspects of antigen design, adjuvant advancement and the development of vaccine delivery systems as they are being applied to malaria vaccines.

Guidelines and considerations for testing malaria vaccines in pregnant women

Author(s): 
Clara Menendez and Pedro Alonso
Reference: 
Human Vaccines, Volume 6, Issue 1, January 2010
Contact email: 
clara.menendez@cresib.cat

Important progress has been made in the last years especially in sub-Saharan Africa, with the introduction of strategies to prevent malaria in pregnancy consisting of intermittent preventive treatment and insecticide treated nets. However, their coverage is still unacceptably low and malaria continues to demand a huge toll on pregnant women and their newborns. Thus, there is a need to explore other preventive strategies such as a vaccine against malaria, which combined with the current tools would maximise the protection efficacy.

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