METHODS FOR THE DETERMINATION OF ANTIBODY IGG AVIDITY, BY COMPARING LIQUID TO SOLID PHASE AVIDITY
The present invention relates to methods of determining anti-infectious agent lgG avidity, for example, human anti-cytomegalovirus and human anti-toxoplasma lgG, using a competitive assay format. The methods include the steps of adding a purified antigen from the infectious agent to a solution to cr...
Gespeichert in:
Hauptverfasser: | , , , , , , |
---|---|
Format: | Patent |
Sprache: | eng ; fre |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | SMITH, DARWIN D., JR CHRIST, HEIKE MARIA PUCCI, DOMINICK L HERZOGENRATH, JOERG CURDT, INGO MAINE, GREGORY T HSU, STEPHEN C |
description | The present invention relates to methods of determining anti-infectious agent lgG avidity, for example, human anti-cytomegalovirus and human anti-toxoplasma lgG, using a competitive assay format. The methods include the steps of adding a purified antigen from the infectious agent to a solution to create a liquid phase antigen, and coating the purified antigen onto a solid phase to create a solid phase antigen; assaying separately the liquid and solid phase antigens with test samples from the patient and determining the formation of antibody/antigen complexes; and determining the ratio of anti-infectious agent antibody present in the test sample when assayed by the liquid phase antigen compared to the solid phase antigen, wherein the ratio is proportional to the level of antibody present in the patient.
La présente invention concerne des procédés de détermination d'avidité pour un IgG anti-agent infectieux, par exemple un IgG anti-cytomégalovirus et anti-toxoplasme humain, utilisant un format de dosage compétitif. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CA2628399C</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CA2628399C</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CA2628399C3</originalsourceid><addsrcrecordid>eNqFyj0KwkAQQOE0FqKewTmANgmIKSf7kx1IdmJ2FFKFRdZKNBDvjxZaW71XfMsstkYc6wCWexBnQBsxfUsehdgDW0AvVLEegOoa8EKaZNhBNYDitsOefA0Nnc6kQRgCN5_pHAbzs-tscYv3OW2-XWVba0S5fZqeY5qneE2P9BoV5of8WJSlKv6LN8lgMqM</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>METHODS FOR THE DETERMINATION OF ANTIBODY IGG AVIDITY, BY COMPARING LIQUID TO SOLID PHASE AVIDITY</title><source>esp@cenet</source><creator>SMITH, DARWIN D., JR ; CHRIST, HEIKE MARIA ; PUCCI, DOMINICK L ; HERZOGENRATH, JOERG ; CURDT, INGO ; MAINE, GREGORY T ; HSU, STEPHEN C</creator><creatorcontrib>SMITH, DARWIN D., JR ; CHRIST, HEIKE MARIA ; PUCCI, DOMINICK L ; HERZOGENRATH, JOERG ; CURDT, INGO ; MAINE, GREGORY T ; HSU, STEPHEN C</creatorcontrib><description>The present invention relates to methods of determining anti-infectious agent lgG avidity, for example, human anti-cytomegalovirus and human anti-toxoplasma lgG, using a competitive assay format. The methods include the steps of adding a purified antigen from the infectious agent to a solution to create a liquid phase antigen, and coating the purified antigen onto a solid phase to create a solid phase antigen; assaying separately the liquid and solid phase antigens with test samples from the patient and determining the formation of antibody/antigen complexes; and determining the ratio of anti-infectious agent antibody present in the test sample when assayed by the liquid phase antigen compared to the solid phase antigen, wherein the ratio is proportional to the level of antibody present in the patient.
La présente invention concerne des procédés de détermination d'avidité pour un IgG anti-agent infectieux, par exemple un IgG anti-cytomégalovirus et anti-toxoplasme humain, utilisant un format de dosage compétitif.</description><language>eng ; fre</language><subject>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES ; MEASURING ; PHYSICS ; TESTING</subject><creationdate>2014</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20140225&DB=EPODOC&CC=CA&NR=2628399C$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20140225&DB=EPODOC&CC=CA&NR=2628399C$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SMITH, DARWIN D., JR</creatorcontrib><creatorcontrib>CHRIST, HEIKE MARIA</creatorcontrib><creatorcontrib>PUCCI, DOMINICK L</creatorcontrib><creatorcontrib>HERZOGENRATH, JOERG</creatorcontrib><creatorcontrib>CURDT, INGO</creatorcontrib><creatorcontrib>MAINE, GREGORY T</creatorcontrib><creatorcontrib>HSU, STEPHEN C</creatorcontrib><title>METHODS FOR THE DETERMINATION OF ANTIBODY IGG AVIDITY, BY COMPARING LIQUID TO SOLID PHASE AVIDITY</title><description>The present invention relates to methods of determining anti-infectious agent lgG avidity, for example, human anti-cytomegalovirus and human anti-toxoplasma lgG, using a competitive assay format. The methods include the steps of adding a purified antigen from the infectious agent to a solution to create a liquid phase antigen, and coating the purified antigen onto a solid phase to create a solid phase antigen; assaying separately the liquid and solid phase antigens with test samples from the patient and determining the formation of antibody/antigen complexes; and determining the ratio of anti-infectious agent antibody present in the test sample when assayed by the liquid phase antigen compared to the solid phase antigen, wherein the ratio is proportional to the level of antibody present in the patient.
La présente invention concerne des procédés de détermination d'avidité pour un IgG anti-agent infectieux, par exemple un IgG anti-cytomégalovirus et anti-toxoplasme humain, utilisant un format de dosage compétitif.</description><subject>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</subject><subject>MEASURING</subject><subject>PHYSICS</subject><subject>TESTING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2014</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFyj0KwkAQQOE0FqKewTmANgmIKSf7kx1IdmJ2FFKFRdZKNBDvjxZaW71XfMsstkYc6wCWexBnQBsxfUsehdgDW0AvVLEegOoa8EKaZNhBNYDitsOefA0Nnc6kQRgCN5_pHAbzs-tscYv3OW2-XWVba0S5fZqeY5qneE2P9BoV5of8WJSlKv6LN8lgMqM</recordid><startdate>20140225</startdate><enddate>20140225</enddate><creator>SMITH, DARWIN D., JR</creator><creator>CHRIST, HEIKE MARIA</creator><creator>PUCCI, DOMINICK L</creator><creator>HERZOGENRATH, JOERG</creator><creator>CURDT, INGO</creator><creator>MAINE, GREGORY T</creator><creator>HSU, STEPHEN C</creator><scope>EVB</scope></search><sort><creationdate>20140225</creationdate><title>METHODS FOR THE DETERMINATION OF ANTIBODY IGG AVIDITY, BY COMPARING LIQUID TO SOLID PHASE AVIDITY</title><author>SMITH, DARWIN D., JR ; CHRIST, HEIKE MARIA ; PUCCI, DOMINICK L ; HERZOGENRATH, JOERG ; CURDT, INGO ; MAINE, GREGORY T ; HSU, STEPHEN C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CA2628399C3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>2014</creationdate><topic>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</topic><topic>MEASURING</topic><topic>PHYSICS</topic><topic>TESTING</topic><toplevel>online_resources</toplevel><creatorcontrib>SMITH, DARWIN D., JR</creatorcontrib><creatorcontrib>CHRIST, HEIKE MARIA</creatorcontrib><creatorcontrib>PUCCI, DOMINICK L</creatorcontrib><creatorcontrib>HERZOGENRATH, JOERG</creatorcontrib><creatorcontrib>CURDT, INGO</creatorcontrib><creatorcontrib>MAINE, GREGORY T</creatorcontrib><creatorcontrib>HSU, STEPHEN C</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SMITH, DARWIN D., JR</au><au>CHRIST, HEIKE MARIA</au><au>PUCCI, DOMINICK L</au><au>HERZOGENRATH, JOERG</au><au>CURDT, INGO</au><au>MAINE, GREGORY T</au><au>HSU, STEPHEN C</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>METHODS FOR THE DETERMINATION OF ANTIBODY IGG AVIDITY, BY COMPARING LIQUID TO SOLID PHASE AVIDITY</title><date>2014-02-25</date><risdate>2014</risdate><abstract>The present invention relates to methods of determining anti-infectious agent lgG avidity, for example, human anti-cytomegalovirus and human anti-toxoplasma lgG, using a competitive assay format. The methods include the steps of adding a purified antigen from the infectious agent to a solution to create a liquid phase antigen, and coating the purified antigen onto a solid phase to create a solid phase antigen; assaying separately the liquid and solid phase antigens with test samples from the patient and determining the formation of antibody/antigen complexes; and determining the ratio of anti-infectious agent antibody present in the test sample when assayed by the liquid phase antigen compared to the solid phase antigen, wherein the ratio is proportional to the level of antibody present in the patient.
La présente invention concerne des procédés de détermination d'avidité pour un IgG anti-agent infectieux, par exemple un IgG anti-cytomégalovirus et anti-toxoplasme humain, utilisant un format de dosage compétitif.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | eng ; fre |
recordid | cdi_epo_espacenet_CA2628399C |
source | esp@cenet |
subjects | INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES MEASURING PHYSICS TESTING |
title | METHODS FOR THE DETERMINATION OF ANTIBODY IGG AVIDITY, BY COMPARING LIQUID TO SOLID PHASE AVIDITY |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T11%3A48%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=SMITH,%20DARWIN%20D.,%20JR&rft.date=2014-02-25&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECA2628399C%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |