The GMZ2 malaria vaccine: from concept to efficacy in humans

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The GMZ2 malaria vaccine: from concept to efficacy in humans. / Theisen, Michael; Adu, Bright; Mordmueller, Benjamin; Singh, Subhash.

I: Expert Review of Vaccines, Bind 16, Nr. 9, 2017, s. 907-917.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Theisen, M, Adu, B, Mordmueller, B & Singh, S 2017, 'The GMZ2 malaria vaccine: from concept to efficacy in humans', Expert Review of Vaccines, bind 16, nr. 9, s. 907-917. https://doi.org/10.1080/14760584.2017.1355246

APA

Theisen, M., Adu, B., Mordmueller, B., & Singh, S. (2017). The GMZ2 malaria vaccine: from concept to efficacy in humans. Expert Review of Vaccines, 16(9), 907-917. https://doi.org/10.1080/14760584.2017.1355246

Vancouver

Theisen M, Adu B, Mordmueller B, Singh S. The GMZ2 malaria vaccine: from concept to efficacy in humans. Expert Review of Vaccines. 2017;16(9):907-917. https://doi.org/10.1080/14760584.2017.1355246

Author

Theisen, Michael ; Adu, Bright ; Mordmueller, Benjamin ; Singh, Subhash. / The GMZ2 malaria vaccine: from concept to efficacy in humans. I: Expert Review of Vaccines. 2017 ; Bind 16, Nr. 9. s. 907-917.

Bibtex

@article{3aabdf5a647446ca9e7d72629464a80d,
title = "The GMZ2 malaria vaccine: from concept to efficacy in humans",
abstract = "Introduction: GMZ2 is a recombinant protein consisting of conserved domains of GLURP and MSP3, two asexual blood-stage antigens of Plasmodium falciparum, and is designed with the aim of mimicking naturally acquired anti-malarial immunity. The rationale for combining these two antigens is based on a series of immune epidemiological studies from geographically diverse malaria endemic regions; functional in vitro studies; and pre-clinical studies in rodents and New World monkeys. GMZ2 adjuvanted with alhydrogel{\textregistered} (alum) was well tolerated and immunogenic in three phase 1 studies. The recently concluded phase 2 trial of GMZ2/alum, involving 1849 participants 12 to 60 month of age in four countries in West, Central and Eastern Africa, showed that GMZ2 is well tolerated and has some, albeit modest, efficacy in the target population.Areas covered: PubMed (www.ncbi.nlm.nih.gov/pubmed) was searched to review the progress and future prospects for clinical development of GMZ2 sub-unit vaccine. We will focus on discovery, naturally acquired immunity, functional activity of specific antibodies, sequence diversity, production, pre-clinical and clinical studies.Expert commentary: GMZ2 is well tolerated and has some, albeit modest, efficacy in the target population. More immunogenic formulations should be developed.",
keywords = "Malaria, naturally acquired immunity, vaccine, cytophilic IgG, GMZ2, GLURP, MSP3",
author = "Michael Theisen and Bright Adu and Benjamin Mordmueller and Subhash Singh",
year = "2017",
doi = "10.1080/14760584.2017.1355246",
language = "English",
volume = "16",
pages = "907--917",
journal = "Expert Review of Vaccines",
issn = "1476-0584",
publisher = "Taylor & Francis",
number = "9",

}

RIS

TY - JOUR

T1 - The GMZ2 malaria vaccine: from concept to efficacy in humans

AU - Theisen, Michael

AU - Adu, Bright

AU - Mordmueller, Benjamin

AU - Singh, Subhash

PY - 2017

Y1 - 2017

N2 - Introduction: GMZ2 is a recombinant protein consisting of conserved domains of GLURP and MSP3, two asexual blood-stage antigens of Plasmodium falciparum, and is designed with the aim of mimicking naturally acquired anti-malarial immunity. The rationale for combining these two antigens is based on a series of immune epidemiological studies from geographically diverse malaria endemic regions; functional in vitro studies; and pre-clinical studies in rodents and New World monkeys. GMZ2 adjuvanted with alhydrogel® (alum) was well tolerated and immunogenic in three phase 1 studies. The recently concluded phase 2 trial of GMZ2/alum, involving 1849 participants 12 to 60 month of age in four countries in West, Central and Eastern Africa, showed that GMZ2 is well tolerated and has some, albeit modest, efficacy in the target population.Areas covered: PubMed (www.ncbi.nlm.nih.gov/pubmed) was searched to review the progress and future prospects for clinical development of GMZ2 sub-unit vaccine. We will focus on discovery, naturally acquired immunity, functional activity of specific antibodies, sequence diversity, production, pre-clinical and clinical studies.Expert commentary: GMZ2 is well tolerated and has some, albeit modest, efficacy in the target population. More immunogenic formulations should be developed.

AB - Introduction: GMZ2 is a recombinant protein consisting of conserved domains of GLURP and MSP3, two asexual blood-stage antigens of Plasmodium falciparum, and is designed with the aim of mimicking naturally acquired anti-malarial immunity. The rationale for combining these two antigens is based on a series of immune epidemiological studies from geographically diverse malaria endemic regions; functional in vitro studies; and pre-clinical studies in rodents and New World monkeys. GMZ2 adjuvanted with alhydrogel® (alum) was well tolerated and immunogenic in three phase 1 studies. The recently concluded phase 2 trial of GMZ2/alum, involving 1849 participants 12 to 60 month of age in four countries in West, Central and Eastern Africa, showed that GMZ2 is well tolerated and has some, albeit modest, efficacy in the target population.Areas covered: PubMed (www.ncbi.nlm.nih.gov/pubmed) was searched to review the progress and future prospects for clinical development of GMZ2 sub-unit vaccine. We will focus on discovery, naturally acquired immunity, functional activity of specific antibodies, sequence diversity, production, pre-clinical and clinical studies.Expert commentary: GMZ2 is well tolerated and has some, albeit modest, efficacy in the target population. More immunogenic formulations should be developed.

KW - Malaria

KW - naturally acquired immunity

KW - vaccine

KW - cytophilic IgG

KW - GMZ2

KW - GLURP

KW - MSP3

U2 - 10.1080/14760584.2017.1355246

DO - 10.1080/14760584.2017.1355246

M3 - Journal article

C2 - 28699823

VL - 16

SP - 907

EP - 917

JO - Expert Review of Vaccines

JF - Expert Review of Vaccines

SN - 1476-0584

IS - 9

ER -

ID: 182580561