Interaction between Shiga Toxin and Monoclonal Antibodies: Binding Characteristics and in Vitro Neutralizing Abilities
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , |
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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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 |
_version_ |
1814268329490120704 |