Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities

Detalhes bibliográficos
Autor(a) principal: Rocha, Leticia B.
Data de Publicação: 2012
Outros Autores: Luz, Daniela E., Moraes, Claudia T. P., Caravelli, Andressa, Fernandes, Irene, Guth, Beatriz Ernestina Cabilio [UNIFESP], Horton, Denise S. P. Q., Piazza, Roxane M. F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.3390/toxins4090729
http://repositorio.unifesp.br/handle/11600/35200
Resumo: Monoclonal antibodies (MAbs) have been employed either for diagnosis or treatment of infections caused by different pathogens. Specifically for Shiga toxin-producing Escherichia coli (STEC), numerous immunoassays have been developed for STEC diagnosis, showing variability in sensitivity and specificity when evaluated by reference laboratories, and no therapy or vaccines are currently approved. Thus, the aim of this work was the characterization of the interaction between MAbs against Stx1 and Stx2 toxins and their neutralizing abilities to enable their use as tools for diagnosis and therapy. the selected clones designated 3E2 (anti-Stx1) and 2E11 (anti-Stx2) were classified as IgG1. 3E2 recognized the B subunit of Stx1 with an affinity constant of 2.5 x 10(-10) M, detected as little as 6.2 ng of Stx1 and was stable up to 50 degrees C. in contrast, 2E11 recognized the A subunit of Stx2, was stable up to 70 degrees C, had a high dissociation constant of 6.1 x 10(-10) M, and detected as little as 12.5 ng of Stx2. Neutralization tests showed that 160 ng of 3E2 MAb inhibited 80% of Stx1 activity and 500 mu g 2E11 MAb were required for 60% inhibition of Stx2 activity. These MAb amounts reversed 25 to 80% of the cytotoxicity triggered by different STEC isolates. in conclusion, these MAbs show suitable characteristics for their use in STEC diagnosis and encourage future studies to investigate their protective efficacy.
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spelling Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing AbilitiesStx1Stx2monoclonal antibodiesbindingstabilitydetectionneutralizing abilityspecificityMonoclonal antibodies (MAbs) have been employed either for diagnosis or treatment of infections caused by different pathogens. Specifically for Shiga toxin-producing Escherichia coli (STEC), numerous immunoassays have been developed for STEC diagnosis, showing variability in sensitivity and specificity when evaluated by reference laboratories, and no therapy or vaccines are currently approved. Thus, the aim of this work was the characterization of the interaction between MAbs against Stx1 and Stx2 toxins and their neutralizing abilities to enable their use as tools for diagnosis and therapy. the selected clones designated 3E2 (anti-Stx1) and 2E11 (anti-Stx2) were classified as IgG1. 3E2 recognized the B subunit of Stx1 with an affinity constant of 2.5 x 10(-10) M, detected as little as 6.2 ng of Stx1 and was stable up to 50 degrees C. in contrast, 2E11 recognized the A subunit of Stx2, was stable up to 70 degrees C, had a high dissociation constant of 6.1 x 10(-10) M, and detected as little as 12.5 ng of Stx2. Neutralization tests showed that 160 ng of 3E2 MAb inhibited 80% of Stx1 activity and 500 mu g 2E11 MAb were required for 60% inhibition of Stx2 activity. These MAb amounts reversed 25 to 80% of the cytotoxicity triggered by different STEC isolates. in conclusion, these MAbs show suitable characteristics for their use in STEC diagnosis and encourage future studies to investigate their protective efficacy.Butantan Inst, Bacteriol Lab, São Paulo, BrazilButantan Inst, Immunopathol Lab, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol, Escola Paulista Med, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Mdpi AgButantan InstUniversidade Federal de São Paulo (UNIFESP)Rocha, Leticia B.Luz, Daniela E.Moraes, Claudia T. P.Caravelli, AndressaFernandes, IreneGuth, Beatriz Ernestina Cabilio [UNIFESP]Horton, Denise S. P. Q.Piazza, Roxane M. F.2016-01-24T14:27:36Z2016-01-24T14:27:36Z2012-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion729-747application/pdfhttp://dx.doi.org/10.3390/toxins4090729Toxins. Basel: Mdpi Ag, v. 4, n. 9, p. 729-747, 2012.10.3390/toxins4090729WOS000315405900007.pdf2072-6651http://repositorio.unifesp.br/handle/11600/35200WOS:000315405900007engToxinsinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T14:31:09Zoai:repositorio.unifesp.br/:11600/35200Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T14:31:09Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
title Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
spellingShingle Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
Rocha, Leticia B.
Stx1
Stx2
monoclonal antibodies
binding
stability
detection
neutralizing ability
specificity
title_short Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
title_full Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
title_fullStr Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
title_full_unstemmed Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
title_sort Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
author Rocha, Leticia B.
author_facet Rocha, Leticia B.
Luz, Daniela E.
Moraes, Claudia T. P.
Caravelli, Andressa
Fernandes, Irene
Guth, Beatriz Ernestina Cabilio [UNIFESP]
Horton, Denise S. P. Q.
Piazza, Roxane M. F.
author_role author
author2 Luz, Daniela E.
Moraes, Claudia T. P.
Caravelli, Andressa
Fernandes, Irene
Guth, Beatriz Ernestina Cabilio [UNIFESP]
Horton, Denise S. P. Q.
Piazza, Roxane M. F.
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Butantan Inst
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Rocha, Leticia B.
Luz, Daniela E.
Moraes, Claudia T. P.
Caravelli, Andressa
Fernandes, Irene
Guth, Beatriz Ernestina Cabilio [UNIFESP]
Horton, Denise S. P. Q.
Piazza, Roxane M. F.
dc.subject.por.fl_str_mv Stx1
Stx2
monoclonal antibodies
binding
stability
detection
neutralizing ability
specificity
topic Stx1
Stx2
monoclonal antibodies
binding
stability
detection
neutralizing ability
specificity
description Monoclonal antibodies (MAbs) have been employed either for diagnosis or treatment of infections caused by different pathogens. Specifically for Shiga toxin-producing Escherichia coli (STEC), numerous immunoassays have been developed for STEC diagnosis, showing variability in sensitivity and specificity when evaluated by reference laboratories, and no therapy or vaccines are currently approved. Thus, the aim of this work was the characterization of the interaction between MAbs against Stx1 and Stx2 toxins and their neutralizing abilities to enable their use as tools for diagnosis and therapy. the selected clones designated 3E2 (anti-Stx1) and 2E11 (anti-Stx2) were classified as IgG1. 3E2 recognized the B subunit of Stx1 with an affinity constant of 2.5 x 10(-10) M, detected as little as 6.2 ng of Stx1 and was stable up to 50 degrees C. in contrast, 2E11 recognized the A subunit of Stx2, was stable up to 70 degrees C, had a high dissociation constant of 6.1 x 10(-10) M, and detected as little as 12.5 ng of Stx2. Neutralization tests showed that 160 ng of 3E2 MAb inhibited 80% of Stx1 activity and 500 mu g 2E11 MAb were required for 60% inhibition of Stx2 activity. These MAb amounts reversed 25 to 80% of the cytotoxicity triggered by different STEC isolates. in conclusion, these MAbs show suitable characteristics for their use in STEC diagnosis and encourage future studies to investigate their protective efficacy.
publishDate 2012
dc.date.none.fl_str_mv 2012-09-01
2016-01-24T14:27:36Z
2016-01-24T14:27:36Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/toxins4090729
Toxins. Basel: Mdpi Ag, v. 4, n. 9, p. 729-747, 2012.
10.3390/toxins4090729
WOS000315405900007.pdf
2072-6651
http://repositorio.unifesp.br/handle/11600/35200
WOS:000315405900007
url http://dx.doi.org/10.3390/toxins4090729
http://repositorio.unifesp.br/handle/11600/35200
identifier_str_mv Toxins. Basel: Mdpi Ag, v. 4, n. 9, p. 729-747, 2012.
10.3390/toxins4090729
WOS000315405900007.pdf
2072-6651
WOS:000315405900007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Toxins
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 729-747
application/pdf
dc.publisher.none.fl_str_mv Mdpi Ag
publisher.none.fl_str_mv Mdpi Ag
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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