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...
- 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 |