Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model

Malaria continues being a high-impact disease regarding public health worldwide; the WHO report for malaria in 2018 estimated that 219 million cases occurred in 2017, mostly caused by the parasite Plasmodium falciparum. The disease cost the lives of more than 400,000 people, mainly in Africa. In spi...

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Autores:
Tipo de recurso:
Fecha de publicación:
2019
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22372
Acceso en línea:
https://doi.org/10.1155/2019/3832513
https://repository.urosario.edu.co/handle/10336/22372
Palabra clave:
Adjuvant
Immune protection inducing protein structure vaccine
Malaria vaccine
Plasmodium falciparum protein
Protozoal protein
Unclassified drug
Animal cell
Animal experiment
Article
Controlled study
Drug formulation
Drug safety
Drug synthesis
Erythrocyte
Female
Humoral immunity
Immunization
Immunogenicity
Immunological tolerance
In vitro study
In vivo study
Malaria falciparum
Male
Merozoite
Mouse
Nonhuman
Plasmodium falciparum
Protein structure
Repeated drug dose
Single drug dose
Vaccine immunogenicity
Rights
License
Abierto (Texto Completo)
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repository_id_str
dc.title.spa.fl_str_mv Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
title Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
spellingShingle Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
Adjuvant
Immune protection inducing protein structure vaccine
Malaria vaccine
Plasmodium falciparum protein
Protozoal protein
Unclassified drug
Animal cell
Animal experiment
Article
Controlled study
Drug formulation
Drug safety
Drug synthesis
Erythrocyte
Female
Humoral immunity
Immunization
Immunogenicity
Immunological tolerance
In vitro study
In vivo study
Malaria falciparum
Male
Merozoite
Mouse
Nonhuman
Plasmodium falciparum
Protein structure
Repeated drug dose
Single drug dose
Vaccine immunogenicity
title_short Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
title_full Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
title_fullStr Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
title_full_unstemmed Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
title_sort Preliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine Model
dc.subject.keyword.spa.fl_str_mv Adjuvant
Immune protection inducing protein structure vaccine
Malaria vaccine
Plasmodium falciparum protein
Protozoal protein
Unclassified drug
Animal cell
Animal experiment
Article
Controlled study
Drug formulation
Drug safety
Drug synthesis
Erythrocyte
Female
Humoral immunity
Immunization
Immunogenicity
Immunological tolerance
In vitro study
In vivo study
Malaria falciparum
Male
Merozoite
Mouse
Nonhuman
Plasmodium falciparum
Protein structure
Repeated drug dose
Single drug dose
Vaccine immunogenicity
topic Adjuvant
Immune protection inducing protein structure vaccine
Malaria vaccine
Plasmodium falciparum protein
Protozoal protein
Unclassified drug
Animal cell
Animal experiment
Article
Controlled study
Drug formulation
Drug safety
Drug synthesis
Erythrocyte
Female
Humoral immunity
Immunization
Immunogenicity
Immunological tolerance
In vitro study
In vivo study
Malaria falciparum
Male
Merozoite
Mouse
Nonhuman
Plasmodium falciparum
Protein structure
Repeated drug dose
Single drug dose
Vaccine immunogenicity
description Malaria continues being a high-impact disease regarding public health worldwide; the WHO report for malaria in 2018 estimated that 219 million cases occurred in 2017, mostly caused by the parasite Plasmodium falciparum. The disease cost the lives of more than 400,000 people, mainly in Africa. In spite of great efforts aimed at developing better prevention (i.e., a highly effective vaccine), diagnosis, and treatment methods for malaria, no efficient solution to this disease has been advanced to date. The Fundación Instituto de Inmunología de Colombia (FIDIC) has been developing studies aimed at furthering the search for vaccine candidates for controlling P. falciparum malaria. However, vaccine development involves safety and immunogenicity studies regarding their formulation in animal models before proceeding to clinical studies. The present work has thus been aimed at evaluating the safety and immunogenicity of a mixture of 23 chemically synthesised, modified peptides (immune protection-inducing protein structure (IMPIPS)) derived from different P. falciparum proteins. Single and repeat dose assays were thus used with male and female BALB/c mice which were immunised with the IMPIPS mixture. It was found that single and repeat dose immunisation with the IMPIPS mixture was safe, both locally and systemically. It was observed that the antibodies so stimulated recognised the parasite's native proteins and inhibited merozoite invasion of red blood cells in vitro when evaluating the humoral immune response induced by the IMPIPS mixture. Such results suggested that the IMPIPS peptide mixture could be a safe candidate to be tested during the next stage involved in developing an antimalarial vaccine, evaluating local safety, immunogenicity, and protection in a nonhuman primate model. © 2019 Jennifer Lambraño et al.
publishDate 2019
dc.date.created.spa.fl_str_mv 2019
dc.date.accessioned.none.fl_str_mv 2020-05-25T23:56:14Z
dc.date.available.none.fl_str_mv 2020-05-25T23:56:14Z
dc.type.eng.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1155/2019/3832513
dc.identifier.issn.none.fl_str_mv 23147156
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dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/22372
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https://repository.urosario.edu.co/handle/10336/22372
identifier_str_mv 23147156
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dc.language.iso.spa.fl_str_mv eng
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dc.relation.citationTitle.none.fl_str_mv Journal of Immunology Research
dc.relation.citationVolume.none.fl_str_mv Vol. 2019
dc.relation.ispartof.spa.fl_str_mv Journal of Immunology Research, ISSN:23147156, 23148861, Vol.2019,(2019)
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dc.publisher.spa.fl_str_mv Hindawi Limited
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spelling 5253847f-17b5-4f86-868d-3d86c6a30a96-191225589-116aa0ab9-4ca4-4d37-97a4-38d5544421a8-1986250b7-49cf-486b-835f-a45e119afc6b-151721018-15e48b055-035f-44d8-9867-a21686777f9d-151894882600796530656002020-05-25T23:56:14Z2020-05-25T23:56:14Z2019Malaria continues being a high-impact disease regarding public health worldwide; the WHO report for malaria in 2018 estimated that 219 million cases occurred in 2017, mostly caused by the parasite Plasmodium falciparum. The disease cost the lives of more than 400,000 people, mainly in Africa. In spite of great efforts aimed at developing better prevention (i.e., a highly effective vaccine), diagnosis, and treatment methods for malaria, no efficient solution to this disease has been advanced to date. The Fundación Instituto de Inmunología de Colombia (FIDIC) has been developing studies aimed at furthering the search for vaccine candidates for controlling P. falciparum malaria. However, vaccine development involves safety and immunogenicity studies regarding their formulation in animal models before proceeding to clinical studies. The present work has thus been aimed at evaluating the safety and immunogenicity of a mixture of 23 chemically synthesised, modified peptides (immune protection-inducing protein structure (IMPIPS)) derived from different P. falciparum proteins. Single and repeat dose assays were thus used with male and female BALB/c mice which were immunised with the IMPIPS mixture. It was found that single and repeat dose immunisation with the IMPIPS mixture was safe, both locally and systemically. It was observed that the antibodies so stimulated recognised the parasite's native proteins and inhibited merozoite invasion of red blood cells in vitro when evaluating the humoral immune response induced by the IMPIPS mixture. Such results suggested that the IMPIPS peptide mixture could be a safe candidate to be tested during the next stage involved in developing an antimalarial vaccine, evaluating local safety, immunogenicity, and protection in a nonhuman primate model. © 2019 Jennifer Lambraño et al.application/pdfhttps://doi.org/10.1155/2019/38325132314715623148861https://repository.urosario.edu.co/handle/10336/22372engHindawi LimitedJournal of Immunology ResearchVol. 2019Journal of Immunology Research, ISSN:23147156, 23148861, Vol.2019,(2019)https://www.scopus.com/inward/record.uri?eid=2-s2.0-85077994868&doi=10.1155%2f2019%2f3832513&partnerID=40&md5=8ee5d79bf42369796bc1c56222f9ec11Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURAdjuvantImmune protection inducing protein structure vaccineMalaria vaccinePlasmodium falciparum proteinProtozoal proteinUnclassified drugAnimal cellAnimal experimentArticleControlled studyDrug formulationDrug safetyDrug synthesisErythrocyteFemaleHumoral immunityImmunizationImmunogenicityImmunological toleranceIn vitro studyIn vivo studyMalaria falciparumMaleMerozoiteMouseNonhumanPlasmodium falciparumProtein structureRepeated drug doseSingle drug doseVaccine immunogenicityPreliminary Evaluation of the Safety and Immunogenicity of an Antimalarial Vaccine Candidate Modified Peptide (IMPIPS) Mixture in a Murine ModelarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Lambraño, JenniferCurtidor, HernandoAvendaño, CatalinaRoa, LeonardoVanegas, MagnoliaPatarroyo, Manuel EDíaz Arévalo, DianaPatarroyo, Manuel A.ORIGINAL3832513.pdfapplication/pdf3970971https://repository.urosario.edu.co/bitstreams/444bc3e8-270e-483d-ac10-9089f69fdd96/download858436f572d294981c0d04d1e91dac54MD51TEXT3832513.pdf.txt3832513.pdf.txtExtracted texttext/plain51405https://repository.urosario.edu.co/bitstreams/974bf2d4-5b0d-4139-bd1e-b6aced51c5aa/download64c1b9cb670ad1cd02b030c814a0d7c9MD52THUMBNAIL3832513.pdf.jpg3832513.pdf.jpgGenerated Thumbnailimage/jpeg4442https://repository.urosario.edu.co/bitstreams/b9bb0bf2-7a80-4b9c-9898-3b3635e1df85/download3f42634a07f2cbadd6a95275048db3feMD5310336/22372oai:repository.urosario.edu.co:10336/223722022-05-02 07:37:14.024663https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co