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Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults
BACKGROUND: The P. falciparum chimeric protein 2.9 (PfCP-2.9) consisting of the sequences of MSP1-19 and AMA-1 (III) is a malaria vaccine candidate that was found to induce inhibitory antibodies in rabbits and monkeys. This was a phase I randomized, single-blind, placebo-controlled, dose-escalation...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276862/ https://www.ncbi.nlm.nih.gov/pubmed/18398475 http://dx.doi.org/10.1371/journal.pone.0001952 |
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author | Hu, Jinhong Chen, Zhihui Gu, Jun Wan, Mobin Shen, Qian Kieny, Marie-Paule He, Jia Li, Zhen Zhang, Qingfeng Reed, Zarifah Hussain Zhu, Yongmei Li, Wenjie Cao, Yang Qu, Li Cao, Zhifang Wang, Qiang Liu, Haitao Pan, Xuegong Huang, Xiudong Zhang, Dongmei Xue, Xiangyang Pan, Weiqing |
author_facet | Hu, Jinhong Chen, Zhihui Gu, Jun Wan, Mobin Shen, Qian Kieny, Marie-Paule He, Jia Li, Zhen Zhang, Qingfeng Reed, Zarifah Hussain Zhu, Yongmei Li, Wenjie Cao, Yang Qu, Li Cao, Zhifang Wang, Qiang Liu, Haitao Pan, Xuegong Huang, Xiudong Zhang, Dongmei Xue, Xiangyang Pan, Weiqing |
author_sort | Hu, Jinhong |
collection | PubMed |
description | BACKGROUND: The P. falciparum chimeric protein 2.9 (PfCP-2.9) consisting of the sequences of MSP1-19 and AMA-1 (III) is a malaria vaccine candidate that was found to induce inhibitory antibodies in rabbits and monkeys. This was a phase I randomized, single-blind, placebo-controlled, dose-escalation study to evaluate the safety and immunogenicity of the PfCP-2.9 formulated with a novel adjuvant Montanide ISA720. Fifty-two subjects were randomly assigned to 4 dose groups of 10 participants, each receiving the test vaccine of 20, 50, 100, or 200 µg respectively, and 1 placebo group of 12 participants receiving the adjuvant only. METHODS AND FINDINGS: The vaccine formulation was shown to be safe and well-tolerated, and none of the participants withdrew. The total incidence of local adverse events (AEs) was 75%, distributed among 58% of the placebo group and 80% of those vaccinated. Among the vaccinated, 65% had events that were mild and 15% experienced moderate AEs. Almost all systemic adverse reactions observed in this study were graded as mild and required no therapy. The participants receiving the test vaccine developed detectable antibody responses which were boosted by the repeated vaccinations. Sixty percent of the vaccinated participants had high ELISA titers (>1∶10,000) of antigen-specific antibodies which could also recognize native parasite proteins in an immunofluorescence assay (IFA). CONCLUSION: This study is the first clinical trial for this candidate and builds on previous investigations supporting PfCP-2.9/ISA720 as a promising blood-stage malaria vaccine. Results demonstrate safety, tolerability (particularly at the lower doses tested) and immunogenicity of the formulation. Further clinical development is ongoing to explore optimizing the dose and schedule of the formulation to decrease reactogenicity without compromising immunogenicity. TRIAL REGISTRATION: Chinese State Food and Drug Administration (SFDA) 2002SL0046; Controlled-Trials.com ISRCTN66850051 [66850051] |
format | Text |
id | pubmed-2276862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22768622008-04-09 Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults Hu, Jinhong Chen, Zhihui Gu, Jun Wan, Mobin Shen, Qian Kieny, Marie-Paule He, Jia Li, Zhen Zhang, Qingfeng Reed, Zarifah Hussain Zhu, Yongmei Li, Wenjie Cao, Yang Qu, Li Cao, Zhifang Wang, Qiang Liu, Haitao Pan, Xuegong Huang, Xiudong Zhang, Dongmei Xue, Xiangyang Pan, Weiqing PLoS One Research Article BACKGROUND: The P. falciparum chimeric protein 2.9 (PfCP-2.9) consisting of the sequences of MSP1-19 and AMA-1 (III) is a malaria vaccine candidate that was found to induce inhibitory antibodies in rabbits and monkeys. This was a phase I randomized, single-blind, placebo-controlled, dose-escalation study to evaluate the safety and immunogenicity of the PfCP-2.9 formulated with a novel adjuvant Montanide ISA720. Fifty-two subjects were randomly assigned to 4 dose groups of 10 participants, each receiving the test vaccine of 20, 50, 100, or 200 µg respectively, and 1 placebo group of 12 participants receiving the adjuvant only. METHODS AND FINDINGS: The vaccine formulation was shown to be safe and well-tolerated, and none of the participants withdrew. The total incidence of local adverse events (AEs) was 75%, distributed among 58% of the placebo group and 80% of those vaccinated. Among the vaccinated, 65% had events that were mild and 15% experienced moderate AEs. Almost all systemic adverse reactions observed in this study were graded as mild and required no therapy. The participants receiving the test vaccine developed detectable antibody responses which were boosted by the repeated vaccinations. Sixty percent of the vaccinated participants had high ELISA titers (>1∶10,000) of antigen-specific antibodies which could also recognize native parasite proteins in an immunofluorescence assay (IFA). CONCLUSION: This study is the first clinical trial for this candidate and builds on previous investigations supporting PfCP-2.9/ISA720 as a promising blood-stage malaria vaccine. Results demonstrate safety, tolerability (particularly at the lower doses tested) and immunogenicity of the formulation. Further clinical development is ongoing to explore optimizing the dose and schedule of the formulation to decrease reactogenicity without compromising immunogenicity. TRIAL REGISTRATION: Chinese State Food and Drug Administration (SFDA) 2002SL0046; Controlled-Trials.com ISRCTN66850051 [66850051] Public Library of Science 2008-04-09 /pmc/articles/PMC2276862/ /pubmed/18398475 http://dx.doi.org/10.1371/journal.pone.0001952 Text en Hu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hu, Jinhong Chen, Zhihui Gu, Jun Wan, Mobin Shen, Qian Kieny, Marie-Paule He, Jia Li, Zhen Zhang, Qingfeng Reed, Zarifah Hussain Zhu, Yongmei Li, Wenjie Cao, Yang Qu, Li Cao, Zhifang Wang, Qiang Liu, Haitao Pan, Xuegong Huang, Xiudong Zhang, Dongmei Xue, Xiangyang Pan, Weiqing Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults |
title | Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults |
title_full | Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults |
title_fullStr | Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults |
title_full_unstemmed | Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults |
title_short | Safety and Immunogenicity of a Malaria Vaccine, Plasmodium falciparum AMA-1/MSP-1 Chimeric Protein Formulated in Montanide ISA 720 in Healthy Adults |
title_sort | safety and immunogenicity of a malaria vaccine, plasmodium falciparum ama-1/msp-1 chimeric protein formulated in montanide isa 720 in healthy adults |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276862/ https://www.ncbi.nlm.nih.gov/pubmed/18398475 http://dx.doi.org/10.1371/journal.pone.0001952 |
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