New dengue antibody assay with unique differential detection of IgG and IgM antibodies

Most of the serological methods, traditional and recent, that have been developed to assess laboratory confirmation of dengue infection, suffer from the need to use separate tests for IgM and for IgG and the need for paired serum specimens in order to establish a clinical interpretation. Moreover, m...

Full description

Autores:
Rivetz, Baruch
Siman-Tov, Dror
Ambal, Elizabeth
Jaramillo, Antonio-Carlos
Ben-Zvi, Ariela
Tartakovsky, Boris
Fish, Falk
Tipo de recurso:
Article of journal
Fecha de publicación:
2009
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/4667
Acceso en línea:
http://hdl.handle.net/20.500.12495/4667
https://doi.org/10.1016/j.clinbiochem.2008.10.017
https://repositorio.unbosque.edu.co
Palabra clave:
Dengue
Primary infection
Secondary infection
Hemagglutination-inhibition
MAC-ELISA
Rights
openAccess
License
Acceso abierto
id UNBOSQUE2_96904d3c55a661fb335f911b15908a96
oai_identifier_str oai:repositorio.unbosque.edu.co:20.500.12495/4667
network_acronym_str UNBOSQUE2
network_name_str Repositorio U. El Bosque
repository_id_str
dc.title.spa.fl_str_mv New dengue antibody assay with unique differential detection of IgG and IgM antibodies
dc.title.translated.spa.fl_str_mv New dengue antibody assay with unique differential detection of IgG and IgM antibodies
title New dengue antibody assay with unique differential detection of IgG and IgM antibodies
spellingShingle New dengue antibody assay with unique differential detection of IgG and IgM antibodies
Dengue
Primary infection
Secondary infection
Hemagglutination-inhibition
MAC-ELISA
title_short New dengue antibody assay with unique differential detection of IgG and IgM antibodies
title_full New dengue antibody assay with unique differential detection of IgG and IgM antibodies
title_fullStr New dengue antibody assay with unique differential detection of IgG and IgM antibodies
title_full_unstemmed New dengue antibody assay with unique differential detection of IgG and IgM antibodies
title_sort New dengue antibody assay with unique differential detection of IgG and IgM antibodies
dc.creator.fl_str_mv Rivetz, Baruch
Siman-Tov, Dror
Ambal, Elizabeth
Jaramillo, Antonio-Carlos
Ben-Zvi, Ariela
Tartakovsky, Boris
Fish, Falk
dc.contributor.author.none.fl_str_mv Rivetz, Baruch
Siman-Tov, Dror
Ambal, Elizabeth
Jaramillo, Antonio-Carlos
Ben-Zvi, Ariela
Tartakovsky, Boris
Fish, Falk
dc.subject.keywords.spa.fl_str_mv Dengue
Primary infection
Secondary infection
Hemagglutination-inhibition
MAC-ELISA
topic Dengue
Primary infection
Secondary infection
Hemagglutination-inhibition
MAC-ELISA
description Most of the serological methods, traditional and recent, that have been developed to assess laboratory confirmation of dengue infection, suffer from the need to use separate tests for IgM and for IgG and the need for paired serum specimens in order to establish a clinical interpretation. Moreover, most of the IgG tests ignore early convalescence as well as past exposure. The objectives of this study is to demonstrate the advantages of the ImmunoComb Dengue BiSpot, a new dengue antibody assay, that detects simultaneously both dengue-specific IgM and IgG, in determining type and status of infection in a single test. Single and paired positive and negative specimens obtained from various dengue-high prevalent regions and from dengue-free areas were used. The specimens were comprised of admission samples of suspected patients and secondary dengue infection individuals, a group of hospital patients, asymptomatic to dengue who originated from dengue high prevalence areas and dengue-negative volunteers. All samples were tested by the ImmunoComb Dengue BiSpot kit along with the gold standard assays of Hemagglutination-inhibition (HAI) and MAC ELISA. Testing 365 gold standard positive specimens from different regions, the ImmunoComb Dengue BiSpot kit revealed sensitivity for IgM of 97.5% and 99.1% for IgG. The IgG was segregated into 2 groups: 86.6% for high titer and 12.5% for low titer of IgG. The overall sensitivity was 98.9%. The overall specificity of the kit, testing 657 samples, mostly from dengue-free area was 97.9%. The higher diagnostic resolution of the Dengue BiSpot test was demonstrated when the performance of the kit on the various groups was compared to the gold standard tests and the dengue status was determined in paired specimens by the new assay. The results of the present studies demonstrate the advantages of ImmunoComb Dengue BiSpot assay as an alternate strategy for the determination of dengue infection status. The combined use of IgM and IgG to discriminate between primary and secondary infections, on one hand, and providing high resolution in distinction of convalescence stage and past infection, on the other hand, endow the kit with improved capacity in assessing the clinical status of a tested individual in a single test.
publishDate 2009
dc.date.issued.none.fl_str_mv 2009
dc.date.accessioned.none.fl_str_mv 2020-11-09T20:12:28Z
dc.date.available.none.fl_str_mv 2020-11-09T20:12:28Z
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.local.none.fl_str_mv Artículo de revista
dc.type.coar.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.driver.none.fl_str_mv info:eu-repo/semantics/article
format http://purl.org/coar/resource_type/c_6501
dc.identifier.issn.none.fl_str_mv 1873-2933
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12495/4667
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.clinbiochem.2008.10.017
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
dc.identifier.reponame.spa.fl_str_mv reponame:Repositorio Institucional Universidad El Bosque
dc.identifier.repourl.none.fl_str_mv https://repositorio.unbosque.edu.co
identifier_str_mv 1873-2933
instname:Universidad El Bosque
reponame:Repositorio Institucional Universidad El Bosque
url http://hdl.handle.net/20.500.12495/4667
https://doi.org/10.1016/j.clinbiochem.2008.10.017
https://repositorio.unbosque.edu.co
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Clinical Biochemistry, 1873-2933, Vol. 42, Nro. 3, 2009 p. 180-184
dc.relation.uri.none.fl_str_mv https://www.sciencedirect.com/science/article/pii/S0009912008005663?via%3Dihub
dc.rights.local.spa.fl_str_mv Acceso abierto
dc.rights.accessrights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
info:eu-repo/semantics/openAccess
Acceso abierto
dc.rights.creativecommons.none.fl_str_mv 2009
rights_invalid_str_mv Acceso abierto
http://purl.org/coar/access_right/c_abf2
2009
eu_rights_str_mv openAccess
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Elsevier
dc.publisher.journal.spa.fl_str_mv Clinical Biochemistry
institution Universidad El Bosque
bitstream.url.fl_str_mv https://repositorio.unbosque.edu.co/bitstreams/07a90ffb-677c-4a52-b023-dcdc7eae0ee5/download
https://repositorio.unbosque.edu.co/bitstreams/41327264-4cd1-4dbf-937e-7090ca8b2e92/download
https://repositorio.unbosque.edu.co/bitstreams/e7a32a1c-a729-4252-bee0-fb26e3b7f528/download
bitstream.checksum.fl_str_mv eabd334c6120d61f23ff94f4cde4e4b0
7210a811635d1799e7c05fee5d259be7
ddeacbfa51558bc6cbf29b67c45f2918
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositorio Institucional Universidad El Bosque
repository.mail.fl_str_mv bibliotecas@biteca.com
_version_ 1814100708073406464
spelling Rivetz, BaruchSiman-Tov, DrorAmbal, ElizabethJaramillo, Antonio-CarlosBen-Zvi, ArielaTartakovsky, BorisFish, Falk2020-11-09T20:12:28Z2020-11-09T20:12:28Z20091873-2933http://hdl.handle.net/20.500.12495/4667https://doi.org/10.1016/j.clinbiochem.2008.10.017instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengElsevierClinical BiochemistryClinical Biochemistry, 1873-2933, Vol. 42, Nro. 3, 2009 p. 180-184https://www.sciencedirect.com/science/article/pii/S0009912008005663?via%3DihubNew dengue antibody assay with unique differential detection of IgG and IgM antibodiesNew dengue antibody assay with unique differential detection of IgG and IgM antibodiesArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85DenguePrimary infectionSecondary infectionHemagglutination-inhibitionMAC-ELISAMost of the serological methods, traditional and recent, that have been developed to assess laboratory confirmation of dengue infection, suffer from the need to use separate tests for IgM and for IgG and the need for paired serum specimens in order to establish a clinical interpretation. Moreover, most of the IgG tests ignore early convalescence as well as past exposure. The objectives of this study is to demonstrate the advantages of the ImmunoComb Dengue BiSpot, a new dengue antibody assay, that detects simultaneously both dengue-specific IgM and IgG, in determining type and status of infection in a single test. Single and paired positive and negative specimens obtained from various dengue-high prevalent regions and from dengue-free areas were used. The specimens were comprised of admission samples of suspected patients and secondary dengue infection individuals, a group of hospital patients, asymptomatic to dengue who originated from dengue high prevalence areas and dengue-negative volunteers. All samples were tested by the ImmunoComb Dengue BiSpot kit along with the gold standard assays of Hemagglutination-inhibition (HAI) and MAC ELISA. Testing 365 gold standard positive specimens from different regions, the ImmunoComb Dengue BiSpot kit revealed sensitivity for IgM of 97.5% and 99.1% for IgG. The IgG was segregated into 2 groups: 86.6% for high titer and 12.5% for low titer of IgG. The overall sensitivity was 98.9%. The overall specificity of the kit, testing 657 samples, mostly from dengue-free area was 97.9%. The higher diagnostic resolution of the Dengue BiSpot test was demonstrated when the performance of the kit on the various groups was compared to the gold standard tests and the dengue status was determined in paired specimens by the new assay. The results of the present studies demonstrate the advantages of ImmunoComb Dengue BiSpot assay as an alternate strategy for the determination of dengue infection status. The combined use of IgM and IgG to discriminate between primary and secondary infections, on one hand, and providing high resolution in distinction of convalescence stage and past infection, on the other hand, endow the kit with improved capacity in assessing the clinical status of a tested individual in a single test.Acceso abiertohttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto2009ORIGINALRivetz_Baruch_2009.pdfRivetz_Baruch_2009.pdfapplication/pdf158957https://repositorio.unbosque.edu.co/bitstreams/07a90ffb-677c-4a52-b023-dcdc7eae0ee5/downloadeabd334c6120d61f23ff94f4cde4e4b0MD51THUMBNAILRivetz_Baruch_2009.pdf.jpgRivetz_Baruch_2009.pdf.jpgimage/jpeg5775https://repositorio.unbosque.edu.co/bitstreams/41327264-4cd1-4dbf-937e-7090ca8b2e92/download7210a811635d1799e7c05fee5d259be7MD52TEXTRivetz_Baruch_2009.pdf.txtRivetz_Baruch_2009.pdf.txtExtracted texttext/plain26216https://repositorio.unbosque.edu.co/bitstreams/e7a32a1c-a729-4252-bee0-fb26e3b7f528/downloadddeacbfa51558bc6cbf29b67c45f2918MD5320.500.12495/4667oai:repositorio.unbosque.edu.co:20.500.12495/46672024-02-06 23:15:09.827restrictedhttps://repositorio.unbosque.edu.coRepositorio Institucional Universidad El Bosquebibliotecas@biteca.com