Specific antibody fragments for the human carcinoembryonic antigen (cea)
The invention refers to mono- and divalent (diabody) single chain Fv (scFv) antibody fragments, obtained by recombinant DNA techniques from the anti-carcinoembryonic antigen (CEA) monoclonal antibody (Mab) CB/ior-CEA.1. This antibody has high affinity for CEA and is employed in the diagnosis and fol...
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creator | NAVARRO LOURDES TATIANA R ALVAREZ JOSE ALBERTO C AVILA MARTA A GAILONDO COWLEY JORGE V GARCIA HANSSEL B ALMEIDA FREYA DE LOS MILAGROS F SEGUI RAQUEL M LOPEZ LUIS JAVIER G CASTRO BORIS ERNESTO A |
description | The invention refers to mono- and divalent (diabody) single chain Fv (scFv) antibody fragments, obtained by recombinant DNA techniques from the anti-carcinoembryonic antigen (CEA) monoclonal antibody (Mab) CB/ior-CEA.1. This antibody has high affinity for CEA and is employed in the diagnosis and follow-up of human colorectal tumors. As the original Mab, the monovalent fragment and the diabody exhibit high affinity for human CEA and recognize an epitope dependent of carbohydrate conservation. The monovalent scFv fragment and the diabody have affinity constants for CEA of (5.0±0.4)x109 L mol-1 and (2.8±0.3)x1010 L mol-1, respectively. These two fragments do not show cross reactivity with human normal cells and tissues, exception made of the normal colonic mucosa, where CEA is occasionally present. The fragments can be produced through the expression in recombinant microorganisms, starting from the cloning of the encoding variable region nucleic acid sequences obtained from the hybridoma that produces Mab CB/ior-CEA.1. As the original Mab, the monovalent scFv and the diabody have the ability to identify in vivo cells that produce human CEA and grow as tumors in mice. The monovalent scFv and the diabody have a molecular size 5 and 2.5 times lower, respectively, than the mouse Mab, and do not have Fc domains, fact this that confers them the potential to better penetrate tissues in vivo and to be less immunogenic in man. |
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This antibody has high affinity for CEA and is employed in the diagnosis and follow-up of human colorectal tumors. As the original Mab, the monovalent fragment and the diabody exhibit high affinity for human CEA and recognize an epitope dependent of carbohydrate conservation. The monovalent scFv fragment and the diabody have affinity constants for CEA of (5.0±0.4)x109 L mol-1 and (2.8±0.3)x1010 L mol-1, respectively. These two fragments do not show cross reactivity with human normal cells and tissues, exception made of the normal colonic mucosa, where CEA is occasionally present. The fragments can be produced through the expression in recombinant microorganisms, starting from the cloning of the encoding variable region nucleic acid sequences obtained from the hybridoma that produces Mab CB/ior-CEA.1. As the original Mab, the monovalent scFv and the diabody have the ability to identify in vivo cells that produce human CEA and grow as tumors in mice. The monovalent scFv and the diabody have a molecular size 5 and 2.5 times lower, respectively, than the mouse Mab, and do not have Fc domains, fact this that confers them the potential to better penetrate tissues in vivo and to be less immunogenic in man.</description><edition>7</edition><language>eng</language><subject>CHEMISTRY ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PEPTIDES ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>2005</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=20050721&DB=EPODOC&CC=US&NR=2005158322A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76294</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20050721&DB=EPODOC&CC=US&NR=2005158322A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NAVARRO LOURDES TATIANA R</creatorcontrib><creatorcontrib>ALVAREZ JOSE ALBERTO C</creatorcontrib><creatorcontrib>AVILA MARTA A</creatorcontrib><creatorcontrib>GAILONDO COWLEY JORGE V</creatorcontrib><creatorcontrib>GARCIA HANSSEL B</creatorcontrib><creatorcontrib>ALMEIDA FREYA DE LOS MILAGROS F</creatorcontrib><creatorcontrib>SEGUI RAQUEL M</creatorcontrib><creatorcontrib>LOPEZ LUIS JAVIER G</creatorcontrib><creatorcontrib>CASTRO BORIS ERNESTO A</creatorcontrib><title>Specific antibody fragments for the human carcinoembryonic antigen (cea)</title><description>The invention refers to mono- and divalent (diabody) single chain Fv (scFv) antibody fragments, obtained by recombinant DNA techniques from the anti-carcinoembryonic antigen (CEA) monoclonal antibody (Mab) CB/ior-CEA.1. This antibody has high affinity for CEA and is employed in the diagnosis and follow-up of human colorectal tumors. As the original Mab, the monovalent fragment and the diabody exhibit high affinity for human CEA and recognize an epitope dependent of carbohydrate conservation. The monovalent scFv fragment and the diabody have affinity constants for CEA of (5.0±0.4)x109 L mol-1 and (2.8±0.3)x1010 L mol-1, respectively. These two fragments do not show cross reactivity with human normal cells and tissues, exception made of the normal colonic mucosa, where CEA is occasionally present. The fragments can be produced through the expression in recombinant microorganisms, starting from the cloning of the encoding variable region nucleic acid sequences obtained from the hybridoma that produces Mab CB/ior-CEA.1. As the original Mab, the monovalent scFv and the diabody have the ability to identify in vivo cells that produce human CEA and grow as tumors in mice. The monovalent scFv and the diabody have a molecular size 5 and 2.5 times lower, respectively, than the mouse Mab, and do not have Fc domains, fact this that confers them the potential to better penetrate tissues in vivo and to be less immunogenic in man.</description><subject>CHEMISTRY</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PEPTIDES</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2005</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPAILkhNzkzLTFZIzCvJTMpPqVRIK0pMz03NKylWSMsvUijJSFXIKM1NzFNITixKzszLT81NKqrMz4PqSE_NU9BITk3U5GFgTUvMKU7lhdLcDMpuriHOHrqpBfnxqcUFicmpeakl8aHBRgYGpoamFsZGRo6GxsSpAgBwazUK</recordid><startdate>20050721</startdate><enddate>20050721</enddate><creator>NAVARRO LOURDES TATIANA R</creator><creator>ALVAREZ JOSE ALBERTO C</creator><creator>AVILA MARTA A</creator><creator>GAILONDO COWLEY JORGE V</creator><creator>GARCIA HANSSEL B</creator><creator>ALMEIDA FREYA DE LOS MILAGROS F</creator><creator>SEGUI RAQUEL M</creator><creator>LOPEZ LUIS JAVIER G</creator><creator>CASTRO BORIS ERNESTO A</creator><scope>EVB</scope></search><sort><creationdate>20050721</creationdate><title>Specific antibody fragments for the human carcinoembryonic antigen (cea)</title><author>NAVARRO LOURDES TATIANA R ; ALVAREZ JOSE ALBERTO C ; AVILA MARTA A ; GAILONDO COWLEY JORGE V ; GARCIA HANSSEL B ; ALMEIDA FREYA DE LOS MILAGROS F ; SEGUI RAQUEL M ; LOPEZ LUIS JAVIER G ; CASTRO BORIS ERNESTO A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US2005158322A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2005</creationdate><topic>CHEMISTRY</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEPTIDES</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><toplevel>online_resources</toplevel><creatorcontrib>NAVARRO LOURDES TATIANA R</creatorcontrib><creatorcontrib>ALVAREZ JOSE ALBERTO C</creatorcontrib><creatorcontrib>AVILA MARTA A</creatorcontrib><creatorcontrib>GAILONDO COWLEY JORGE V</creatorcontrib><creatorcontrib>GARCIA HANSSEL B</creatorcontrib><creatorcontrib>ALMEIDA FREYA DE LOS MILAGROS F</creatorcontrib><creatorcontrib>SEGUI RAQUEL M</creatorcontrib><creatorcontrib>LOPEZ LUIS JAVIER G</creatorcontrib><creatorcontrib>CASTRO BORIS ERNESTO A</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NAVARRO LOURDES TATIANA R</au><au>ALVAREZ JOSE ALBERTO C</au><au>AVILA MARTA A</au><au>GAILONDO COWLEY JORGE V</au><au>GARCIA HANSSEL B</au><au>ALMEIDA FREYA DE LOS MILAGROS F</au><au>SEGUI RAQUEL M</au><au>LOPEZ LUIS JAVIER G</au><au>CASTRO BORIS ERNESTO A</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Specific antibody fragments for the human carcinoembryonic antigen (cea)</title><date>2005-07-21</date><risdate>2005</risdate><abstract>The invention refers to mono- and divalent (diabody) single chain Fv (scFv) antibody fragments, obtained by recombinant DNA techniques from the anti-carcinoembryonic antigen (CEA) monoclonal antibody (Mab) CB/ior-CEA.1. This antibody has high affinity for CEA and is employed in the diagnosis and follow-up of human colorectal tumors. As the original Mab, the monovalent fragment and the diabody exhibit high affinity for human CEA and recognize an epitope dependent of carbohydrate conservation. The monovalent scFv fragment and the diabody have affinity constants for CEA of (5.0±0.4)x109 L mol-1 and (2.8±0.3)x1010 L mol-1, respectively. These two fragments do not show cross reactivity with human normal cells and tissues, exception made of the normal colonic mucosa, where CEA is occasionally present. The fragments can be produced through the expression in recombinant microorganisms, starting from the cloning of the encoding variable region nucleic acid sequences obtained from the hybridoma that produces Mab CB/ior-CEA.1. As the original Mab, the monovalent scFv and the diabody have the ability to identify in vivo cells that produce human CEA and grow as tumors in mice. The monovalent scFv and the diabody have a molecular size 5 and 2.5 times lower, respectively, than the mouse Mab, and do not have Fc domains, fact this that confers them the potential to better penetrate tissues in vivo and to be less immunogenic in man.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PEPTIDES PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES |
title | Specific antibody fragments for the human carcinoembryonic antigen (cea) |
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