A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1038/s41598-019-52506-w http://hdl.handle.net/11449/196300 |
Resumo: | A precise diagnosis for neuromyelitis optica spectrum disorders (NMOSD) is crucial to improve patients' prognostic, which requires highly specific and sensitive tests. The cell-based assay with a sensitivity of 76% and specificity of 100% is the most recommended test to detect anti-aquaporin-4 antibodies (AQP4-Ab). Here, we tested four AQP4 external loop peptides (AQP4(61-70), AQP4(131-140), AQP4(141-150), and AQP4(201-210)) with an atomic force microscopy nanoimmunosensor to develop a diagnostic assay. We obtained the highest reactivity with AQP4(61-70)-nanoimunosensor. This assay was effective in detecting AQP4-Ab in sera of NMOSD patients with 100% specificity (95% CI 63.06-100), determined by the cut-off adhesion force value of 241.3 pN. NMOSD patients were successfully discriminated from a set of healthy volunteers, patients with multiple sclerosis, and AQP4-Ab-negative patients. AQP4(61-70) sensitivity was 81.25% (95% CI 56.50-99.43), slightly higher than with the CBA method. The results with the AQP4(61-70)-nanoimmunosensor indicate that the differences between NMOSD seropositive and seronegative phenotypes are related to disease-specific epitopes. The absence of AQP4-Ab in sera of NMOSD AQP4-Ab-negative patients may be interpreted by assuming the existence of another potential AQP4 peptide sequence or non-AQP4 antigens as the antibody target. |
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A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disordersA precise diagnosis for neuromyelitis optica spectrum disorders (NMOSD) is crucial to improve patients' prognostic, which requires highly specific and sensitive tests. The cell-based assay with a sensitivity of 76% and specificity of 100% is the most recommended test to detect anti-aquaporin-4 antibodies (AQP4-Ab). Here, we tested four AQP4 external loop peptides (AQP4(61-70), AQP4(131-140), AQP4(141-150), and AQP4(201-210)) with an atomic force microscopy nanoimmunosensor to develop a diagnostic assay. We obtained the highest reactivity with AQP4(61-70)-nanoimunosensor. This assay was effective in detecting AQP4-Ab in sera of NMOSD patients with 100% specificity (95% CI 63.06-100), determined by the cut-off adhesion force value of 241.3 pN. NMOSD patients were successfully discriminated from a set of healthy volunteers, patients with multiple sclerosis, and AQP4-Ab-negative patients. AQP4(61-70) sensitivity was 81.25% (95% CI 56.50-99.43), slightly higher than with the CBA method. The results with the AQP4(61-70)-nanoimmunosensor indicate that the differences between NMOSD seropositive and seronegative phenotypes are related to disease-specific epitopes. The absence of AQP4-Ab in sera of NMOSD AQP4-Ab-negative patients may be interpreted by assuming the existence of another potential AQP4 peptide sequence or non-AQP4 antigens as the antibody target.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Brazil National Council for Scientific and Technological DevelopmentNational Institute for Science and Technology on Organic Electronics -INEOUniv Sao Paulo, Inst Trop Med Sao Paulo, BR-05403000 Sao Paulo, SP, BrazilUniv Fed Sao Carlos, Dept Phys Chem & Math, BR-18052780 Sorocaba, SP, BrazilUniv Fed Sao Carlos, Nanoneurobiophys Res Grp GNN, BR-18052780 Sorocaba, SP, BrazilSao Paulo State Univ, Dept Neurol Psychol & Psychiat, BR-18618687 Botucatu, SP, BrazilUniv Sao Paulo, Sao Carlos Inst Phys, BR-13560970 Sao Carlos, SP, BrazilRheabiotech Lab Res & Dev, Campinas, SP, BrazilUniv Sao Paulo, Inst Chem, Dept Biochem, BR-05508000 Sao Paulo, BrazilUniv Sao Paulo, Ribeirao Preto Med Sch, Dept Neurosci & Behav Sci, Ribeirao Preto, SP, BrazilSao Paulo State Univ, Dept Neurol Psychol & Psychiat, BR-18618687 Botucatu, SP, BrazilFAPESP: FAPESP 2013/14262-7FAPESP: 2015/05283-6FAPESP: 2015/06847-0FAPESP: 2014/12082-4FAPESP: 2014/15093-7FAPESP: 2016/19387-0FAPESP: 2015/36143-2FAPESP: 2015/14360-4FAPESP: 2012/50839-4CAPES: 001Brazil National Council for Scientific and Technological Development: CNPq 305069/2016-0Brazil National Council for Scientific and Technological Development: 459768/2014-0Brazil National Council for Scientific and Technological Development: 308570/2018-9Brazil National Council for Scientific and Technological Development: 308658/2015-9National Institute for Science and Technology on Organic Electronics -INEO: CNPq 465572/2014-6National Institute for Science and Technology on Organic Electronics -INEO: FAPESP 2014/50869-6National Institute for Science and Technology on Organic Electronics -INEO: CAPES 23038.000776/201754Nature Publishing GroupUniversidade de São Paulo (USP)Universidade Federal de São Carlos (UFSCar)Universidade Estadual Paulista (Unesp)Rheabiotech Lab Res & DevMoraes, Ariana de SouzaBrum, Doralina Guimaraes [UNESP]Magalhaes Ierich, Jessica CristianeHiga, Akemi MartinsJabur Assis, Amanda StefanieMiyazaki, Celina MassumiShimizu, Flavio MakotoPeroni, Luis AntonioMachini, M. TeresaBarreira, Amilton AntunesFerreira, MarystelaOliveira Jr, Osvaldo N.Leite, Fabio Lima2020-12-10T19:40:10Z2020-12-10T19:40:10Z2019-11-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article9http://dx.doi.org/10.1038/s41598-019-52506-wScientific Reports. London: Nature Publishing Group, v. 9, 9 p., 2019.2045-2322http://hdl.handle.net/11449/19630010.1038/s41598-019-52506-wWOS:000494636500025Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengScientific Reportsinfo:eu-repo/semantics/openAccess2024-08-16T15:46:17Zoai:repositorio.unesp.br:11449/196300Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-16T15:46:17Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders |
title |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders |
spellingShingle |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders Moraes, Ariana de Souza |
title_short |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders |
title_full |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders |
title_fullStr |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders |
title_full_unstemmed |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders |
title_sort |
A highly specific and sensitive nanoimmunosensor for the diagnosis of neuromyelitis optica spectrum disorders |
author |
Moraes, Ariana de Souza |
author_facet |
Moraes, Ariana de Souza Brum, Doralina Guimaraes [UNESP] Magalhaes Ierich, Jessica Cristiane Higa, Akemi Martins Jabur Assis, Amanda Stefanie Miyazaki, Celina Massumi Shimizu, Flavio Makoto Peroni, Luis Antonio Machini, M. Teresa Barreira, Amilton Antunes Ferreira, Marystela Oliveira Jr, Osvaldo N. Leite, Fabio Lima |
author_role |
author |
author2 |
Brum, Doralina Guimaraes [UNESP] Magalhaes Ierich, Jessica Cristiane Higa, Akemi Martins Jabur Assis, Amanda Stefanie Miyazaki, Celina Massumi Shimizu, Flavio Makoto Peroni, Luis Antonio Machini, M. Teresa Barreira, Amilton Antunes Ferreira, Marystela Oliveira Jr, Osvaldo N. Leite, Fabio Lima |
author2_role |
author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Federal de São Carlos (UFSCar) Universidade Estadual Paulista (Unesp) Rheabiotech Lab Res & Dev |
dc.contributor.author.fl_str_mv |
Moraes, Ariana de Souza Brum, Doralina Guimaraes [UNESP] Magalhaes Ierich, Jessica Cristiane Higa, Akemi Martins Jabur Assis, Amanda Stefanie Miyazaki, Celina Massumi Shimizu, Flavio Makoto Peroni, Luis Antonio Machini, M. Teresa Barreira, Amilton Antunes Ferreira, Marystela Oliveira Jr, Osvaldo N. Leite, Fabio Lima |
description |
A precise diagnosis for neuromyelitis optica spectrum disorders (NMOSD) is crucial to improve patients' prognostic, which requires highly specific and sensitive tests. The cell-based assay with a sensitivity of 76% and specificity of 100% is the most recommended test to detect anti-aquaporin-4 antibodies (AQP4-Ab). Here, we tested four AQP4 external loop peptides (AQP4(61-70), AQP4(131-140), AQP4(141-150), and AQP4(201-210)) with an atomic force microscopy nanoimmunosensor to develop a diagnostic assay. We obtained the highest reactivity with AQP4(61-70)-nanoimunosensor. This assay was effective in detecting AQP4-Ab in sera of NMOSD patients with 100% specificity (95% CI 63.06-100), determined by the cut-off adhesion force value of 241.3 pN. NMOSD patients were successfully discriminated from a set of healthy volunteers, patients with multiple sclerosis, and AQP4-Ab-negative patients. AQP4(61-70) sensitivity was 81.25% (95% CI 56.50-99.43), slightly higher than with the CBA method. The results with the AQP4(61-70)-nanoimmunosensor indicate that the differences between NMOSD seropositive and seronegative phenotypes are related to disease-specific epitopes. The absence of AQP4-Ab in sera of NMOSD AQP4-Ab-negative patients may be interpreted by assuming the existence of another potential AQP4 peptide sequence or non-AQP4 antigens as the antibody target. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-11-06 2020-12-10T19:40:10Z 2020-12-10T19:40:10Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1038/s41598-019-52506-w Scientific Reports. London: Nature Publishing Group, v. 9, 9 p., 2019. 2045-2322 http://hdl.handle.net/11449/196300 10.1038/s41598-019-52506-w WOS:000494636500025 |
url |
http://dx.doi.org/10.1038/s41598-019-52506-w http://hdl.handle.net/11449/196300 |
identifier_str_mv |
Scientific Reports. London: Nature Publishing Group, v. 9, 9 p., 2019. 2045-2322 10.1038/s41598-019-52506-w WOS:000494636500025 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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Scientific Reports |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
9 |
dc.publisher.none.fl_str_mv |
Nature Publishing Group |
publisher.none.fl_str_mv |
Nature Publishing Group |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
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1808128204721881088 |