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Published in: Malaria Journal 1/2016

Open Access 01-12-2016 | Research

Phase 1 randomized controlled trial to evaluate the safety and immunogenicity of recombinant Pichia pastoris-expressed Plasmodium falciparum apical membrane antigen 1 (PfAMA1-FVO [25-545]) in healthy Malian adults in Bandiagara

Authors: Mahamadou A. Thera, Drissa Coulibaly, Abdoulaye K. Kone, Ando B. Guindo, Karim Traore, Abdourhamane H. Sall, Issa Diarra, Modibo Daou, Idrissa M. Traore, Youssouf Tolo, Mady Sissoko, Amadou Niangaly, Charles Arama, Mounirou Baby, Bourema Kouriba, Mahamadou S. Sissoko, Issaka Sagara, Ousmane B. Toure, Amagana Dolo, Dapa A. Diallo, Edmond Remarque, Roma Chilengi, Ramadhani Noor, Sanie Sesay, Alan Thomas, Clemens H. Kocken, Bart W. Faber, Egeruan Babatunde Imoukhuede, Odile Leroy, Ogobara K. Doumbo

Published in: Malaria Journal | Issue 1/2016

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Abstract

Background

The safety and immunogenicity of PfAMA1, adjuvanted with Alhydrogel® was assessed in malaria–experienced Malian adults. The malaria vaccine, PfAMA1-FVO [25-545] is a recombinant protein Pichia pastoris-expressed AMA-1 from Plasmodium falciparum FVO clone adsorbed to Alhydrogel®, the control vaccine was tetanus toxoid produced from formaldehyde detoxified and purified tetanus toxin.

Methods

A double blind randomized controlled phase 1 study enrolled and followed 40 healthy adults aged 18–55 years in Bandiagara, Mali, West Africa, a rural setting with intense seasonal transmission of P. falciparum malaria. Volunteers were randomized to receive either 50 µg of malaria vaccine or the control vaccine. Three doses of vaccine were given on Days 0, 28 and 56, and participants were followed for 1 year. Solicited symptoms were assessed for seven days and unsolicited symptoms for 28 days after each vaccination. Serious adverse events were assessed throughout the study. The titres of anti-AMA-1 antibodies were measured by ELISA and P. falciparum growth inhibition assays were performed.

Results

Commonest local solicited adverse events were the injection site pain and swelling more frequent in the PfAMA1 group. No vaccine related serious adverse events were reported. A significant 3.5-fold increase of anti-AMA-1 IgG antibodies was observed in malaria vaccine recipients four weeks after the third immunization compared to the control group.

Conclusion

The PfAMA1 showed a good safety profile. Most adverse events reported were of mild to moderate intensity. In addition, the vaccine induced a significant though short-lived increase in the anti-AMA1 IgG titres.
Registered on www.​clinicaltrials.​gov with the number NCT00431808
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Metadata
Title
Phase 1 randomized controlled trial to evaluate the safety and immunogenicity of recombinant Pichia pastoris-expressed Plasmodium falciparum apical membrane antigen 1 (PfAMA1-FVO [25-545]) in healthy Malian adults in Bandiagara
Authors
Mahamadou A. Thera
Drissa Coulibaly
Abdoulaye K. Kone
Ando B. Guindo
Karim Traore
Abdourhamane H. Sall
Issa Diarra
Modibo Daou
Idrissa M. Traore
Youssouf Tolo
Mady Sissoko
Amadou Niangaly
Charles Arama
Mounirou Baby
Bourema Kouriba
Mahamadou S. Sissoko
Issaka Sagara
Ousmane B. Toure
Amagana Dolo
Dapa A. Diallo
Edmond Remarque
Roma Chilengi
Ramadhani Noor
Sanie Sesay
Alan Thomas
Clemens H. Kocken
Bart W. Faber
Egeruan Babatunde Imoukhuede
Odile Leroy
Ogobara K. Doumbo
Publication date
01-12-2016
Publisher
BioMed Central
Published in
Malaria Journal / Issue 1/2016
Electronic ISSN: 1475-2875
DOI
https://doi.org/10.1186/s12936-016-1466-4

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