Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection

Although largely considered benign, Plasmodium vivax causes disease in nearly 75 million people each year and the available strategies are not sufficient to reduce the burden of disease, therefore pointing to vaccine development as a cost-effective control measure. In this study, the P. vivax merozo...

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Autores:
Tipo de recurso:
Fecha de publicación:
2009
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/23453
Acceso en línea:
https://doi.org/10.1016/j.vaccine.2009.09.046
https://repository.urosario.edu.co/handle/10336/23453
Palabra clave:
Adjuvant
Aluminum hydroxide
Antibody
Chloroquine
Emulsifying agent
Freund adjuvant
Montanide isa720
Protein
Recombinant merozoite surface protein 10
Recombinant protein
Unclassified drug
Adjuvant therapy
Affinity chromatography
Animal experiment
Animal model
Antibody production
Antibody titer
Aotus
Article
Controlled study
Drug antigenicity
Drug efficacy
Drug formulation
Immunity
Immunogenicity
Malaria
Nonhuman
Plasmodium vivax
Priority journal
Protein expression
Protein purification
Schizont
Serum
Vaccination
Aluminum hydroxide
Animals
Aotus trivirgatus
Freund's adjuvant
Humans
Malaria vaccines
Mannitol
Oleic acids
Plasmodium vivax
Protozoan proteins
Recombinant proteins
Adjuvants
Merozoite surface proteins (msps)
Plasmodium vivax
Vaccine
protozoan
protozoan
immunologic
humoral
vivax
Adjuvants
Antibodies
Antigens
Immunity
Malaria
Rights
License
Abierto (Texto Completo)
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spelling e5f1cbf1-23e3-4d81-8133-988255004a6e-11a837cee-dfa1-42d9-9f6c-31cbb52d5383-100205185-8f0a-42f9-b55f-92d6b99f5c4a-1914e954b-fc69-43d1-8b0b-ddda45ad991a-1faaf745c-61cf-4170-a36f-07c6154b327c-179653065-12020-05-26T00:02:09Z2020-05-26T00:02:09Z2009Although largely considered benign, Plasmodium vivax causes disease in nearly 75 million people each year and the available strategies are not sufficient to reduce the burden of disease, therefore pointing to vaccine development as a cost-effective control measure. In this study, the P. vivax merozoite surface protein 10 (MSP-10) was expressed as a recombinant protein in Escherichia coli and purified by affinity chromatography. High antigenicity was observed since sera from P. vivax-infected patients strongly recognized rPvMSP10. The immunogenicity of rPvMSP10 was tested in Aotus monkeys, comparing responses induced by formulations with Freund's adjuvant, Montanide ISA720 or aluminum hydroxide. All formulations produced high antibody titers recognizing the native protein in late schizonts. Despite inducing strong antibody production, none of the formulations protected immunized Aotus monkeys upon experimental challenge. © 2009 Elsevier Ltd. All rights reserved.application/pdfhttps://doi.org/10.1016/j.vaccine.2009.09.0460264410X13588745https://repository.urosario.edu.co/handle/10336/23453eng13No. 17VaccineVol. 28Vaccine, ISSN:0264410X, 13588745, Vol.28, No.1 (2009); pp. 7-13https://www.scopus.com/inward/record.uri?eid=2-s2.0-70649115450&doi=10.1016%2fj.vaccine.2009.09.046&partnerID=40&md5=ef33b246dba86a7d95eaad963df9037aAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURAdjuvantAluminum hydroxideAntibodyChloroquineEmulsifying agentFreund adjuvantMontanide isa720ProteinRecombinant merozoite surface protein 10Recombinant proteinUnclassified drugAdjuvant therapyAffinity chromatographyAnimal experimentAnimal modelAntibody productionAntibody titerAotusArticleControlled studyDrug antigenicityDrug efficacyDrug formulationImmunityImmunogenicityMalariaNonhumanPlasmodium vivaxPriority journalProtein expressionProtein purificationSchizontSerumVaccinationAluminum hydroxideAnimalsAotus trivirgatusFreund's adjuvantHumansMalaria vaccinesMannitolOleic acidsPlasmodium vivaxProtozoan proteinsRecombinant proteinsAdjuvantsMerozoite surface proteins (msps)Plasmodium vivaxVaccineprotozoanprotozoanimmunologichumoralvivaxAdjuvantsAntibodiesAntigensImmunityMalariaVaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protectionarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Giraldo, Manuel A.Arevalo-Pinzon, GabrielaRojas-Caraballo, JoseMongui, AlvaroRodriguez, RaulPatarroyo, Manuel A.ORIGINALVaccination_with_recombinant_Plasmodium.pdfapplication/pdf5286038https://repository.urosario.edu.co/bitstreams/29ac86ff-d817-47e2-b74c-1c759c315b59/download105b910e02858cc59cc9fc278bc03898MD51TEXTVaccination_with_recombinant_Plasmodium.pdf.txtVaccination_with_recombinant_Plasmodium.pdf.txtExtracted texttext/plain30247https://repository.urosario.edu.co/bitstreams/996a4c46-6221-46ff-a281-79b36384dfcf/download2168b757ff5a2e85db3ac9da524554a7MD52THUMBNAILVaccination_with_recombinant_Plasmodium.pdf.jpgVaccination_with_recombinant_Plasmodium.pdf.jpgGenerated Thumbnailimage/jpeg4720https://repository.urosario.edu.co/bitstreams/0bbe1f32-6b57-48d5-bb4e-bdae1758548d/downloadb825c32d4418601ab6013791a26072c8MD5310336/23453oai:repository.urosario.edu.co:10336/234532022-05-02 07:37:20.975386https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
title Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
spellingShingle Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
Adjuvant
Aluminum hydroxide
Antibody
Chloroquine
Emulsifying agent
Freund adjuvant
Montanide isa720
Protein
Recombinant merozoite surface protein 10
Recombinant protein
Unclassified drug
Adjuvant therapy
Affinity chromatography
Animal experiment
Animal model
Antibody production
Antibody titer
Aotus
Article
Controlled study
Drug antigenicity
Drug efficacy
Drug formulation
Immunity
Immunogenicity
Malaria
Nonhuman
Plasmodium vivax
Priority journal
Protein expression
Protein purification
Schizont
Serum
Vaccination
Aluminum hydroxide
Animals
Aotus trivirgatus
Freund's adjuvant
Humans
Malaria vaccines
Mannitol
Oleic acids
Plasmodium vivax
Protozoan proteins
Recombinant proteins
Adjuvants
Merozoite surface proteins (msps)
Plasmodium vivax
Vaccine
protozoan
protozoan
immunologic
humoral
vivax
Adjuvants
Antibodies
Antigens
Immunity
Malaria
title_short Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
title_full Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
title_fullStr Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
title_full_unstemmed Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
title_sort Vaccination with recombinant Plasmodium vivax MSP-10 formulated in different adjuvants induces strong immunogenicity but no protection
dc.subject.keyword.spa.fl_str_mv Adjuvant
Aluminum hydroxide
Antibody
Chloroquine
Emulsifying agent
Freund adjuvant
Montanide isa720
Protein
Recombinant merozoite surface protein 10
Recombinant protein
Unclassified drug
Adjuvant therapy
Affinity chromatography
Animal experiment
Animal model
Antibody production
Antibody titer
Aotus
Article
Controlled study
Drug antigenicity
Drug efficacy
Drug formulation
Immunity
Immunogenicity
Malaria
Nonhuman
Plasmodium vivax
Priority journal
Protein expression
Protein purification
Schizont
Serum
Vaccination
Aluminum hydroxide
Animals
Aotus trivirgatus
Freund's adjuvant
Humans
Malaria vaccines
Mannitol
Oleic acids
Plasmodium vivax
Protozoan proteins
Recombinant proteins
Adjuvants
Merozoite surface proteins (msps)
Plasmodium vivax
Vaccine
topic Adjuvant
Aluminum hydroxide
Antibody
Chloroquine
Emulsifying agent
Freund adjuvant
Montanide isa720
Protein
Recombinant merozoite surface protein 10
Recombinant protein
Unclassified drug
Adjuvant therapy
Affinity chromatography
Animal experiment
Animal model
Antibody production
Antibody titer
Aotus
Article
Controlled study
Drug antigenicity
Drug efficacy
Drug formulation
Immunity
Immunogenicity
Malaria
Nonhuman
Plasmodium vivax
Priority journal
Protein expression
Protein purification
Schizont
Serum
Vaccination
Aluminum hydroxide
Animals
Aotus trivirgatus
Freund's adjuvant
Humans
Malaria vaccines
Mannitol
Oleic acids
Plasmodium vivax
Protozoan proteins
Recombinant proteins
Adjuvants
Merozoite surface proteins (msps)
Plasmodium vivax
Vaccine
protozoan
protozoan
immunologic
humoral
vivax
Adjuvants
Antibodies
Antigens
Immunity
Malaria
dc.subject.keyword.eng.fl_str_mv protozoan
protozoan
immunologic
humoral
vivax
Adjuvants
Antibodies
Antigens
Immunity
Malaria
description Although largely considered benign, Plasmodium vivax causes disease in nearly 75 million people each year and the available strategies are not sufficient to reduce the burden of disease, therefore pointing to vaccine development as a cost-effective control measure. In this study, the P. vivax merozoite surface protein 10 (MSP-10) was expressed as a recombinant protein in Escherichia coli and purified by affinity chromatography. High antigenicity was observed since sera from P. vivax-infected patients strongly recognized rPvMSP10. The immunogenicity of rPvMSP10 was tested in Aotus monkeys, comparing responses induced by formulations with Freund's adjuvant, Montanide ISA720 or aluminum hydroxide. All formulations produced high antibody titers recognizing the native protein in late schizonts. Despite inducing strong antibody production, none of the formulations protected immunized Aotus monkeys upon experimental challenge. © 2009 Elsevier Ltd. All rights reserved.
publishDate 2009
dc.date.created.spa.fl_str_mv 2009
dc.date.accessioned.none.fl_str_mv 2020-05-26T00:02:09Z
dc.date.available.none.fl_str_mv 2020-05-26T00:02:09Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.vaccine.2009.09.046
dc.identifier.issn.none.fl_str_mv 0264410X
13588745
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/23453
url https://doi.org/10.1016/j.vaccine.2009.09.046
https://repository.urosario.edu.co/handle/10336/23453
identifier_str_mv 0264410X
13588745
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 13
dc.relation.citationIssue.none.fl_str_mv No. 1
dc.relation.citationStartPage.none.fl_str_mv 7
dc.relation.citationTitle.none.fl_str_mv Vaccine
dc.relation.citationVolume.none.fl_str_mv Vol. 28
dc.relation.ispartof.spa.fl_str_mv Vaccine, ISSN:0264410X, 13588745, Vol.28, No.1 (2009); pp. 7-13
dc.relation.uri.spa.fl_str_mv https://www.scopus.com/inward/record.uri?eid=2-s2.0-70649115450&doi=10.1016%2fj.vaccine.2009.09.046&partnerID=40&md5=ef33b246dba86a7d95eaad963df9037a
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dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
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