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The INNs and outs of antibody nonproprietary names
An important step in drug development is the assignment of an International Nonproprietary Name (INN) by the World Health Organization (WHO) that provides healthcare professionals with a unique and universally available designated name to identify each pharmaceutical substance. Monoclonal antibody I...
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Published in: | mAbs 2016-01, Vol.8 (1), p.1-9 |
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creator | Jones, Tim D. Carter, Paul J. Plückthun, Andreas Vásquez, Max Holgate, Robert G.E. Hötzel, Isidro Popplewell, Andrew G. Parren, Paul W.H.I. Enzelberger, Markus Rademaker, Hendrik J. Clark, Michael R. Lowe, David C. Dahiyat, Bassil I. Smith, Victoria Lambert, John M. Wu, Herren Reilly, Mary Haurum, John S. Dübel, Stefan Huston, James S. Schirrmann, Thomas Janssen, Richard A.J. Steegmaier, Martin Gross, Jane A. Bradbury, Andrew R.M. Burton, Dennis R. Dimitrov, Dimiter S. Chester, Kerry A. Glennie, Martin J. Davies, Julian Walker, Adam Martin, Steve McCafferty, John Baker, Matthew P. |
description | An important step in drug development is the assignment of an International Nonproprietary Name (INN) by the World Health Organization (WHO) that provides healthcare professionals with a unique and universally available designated name to identify each pharmaceutical substance. Monoclonal antibody INNs comprise a -mab suffix preceded by a substem indicating the antibody type, e.g., chimeric (-xi-), humanized (-zu-), or human (-u-). The WHO publishes INN definitions that specify how new monoclonal antibody therapeutics are categorized and adapts the definitions to new technologies. However, rapid progress in antibody technologies has blurred the boundaries between existing antibody categories and created a burgeoning array of new antibody formats. Thus, revising the INN system for antibodies is akin to aiming for a rapidly moving target. The WHO recently revised INN definitions for antibodies now to be based on amino acid sequence identity. These new definitions, however, are critically flawed as they are ambiguous and go against decades of scientific literature. A key concern is the imposition of an arbitrary threshold for identity against human germline antibody variable region sequences. This leads to inconsistent classification of somatically mutated human antibodies, humanized antibodies as well as antibodies derived from semi-synthetic/synthetic libraries and transgenic animals. Such sequence-based classification implies clear functional distinction between categories (e.g., immunogenicity). However, there is no scientific evidence to support this. Dialog between the WHO INN Expert Group and key stakeholders is needed to develop a new INN system for antibodies and to avoid confusion and miscommunication between researchers and clinicians prescribing antibodies. |
doi_str_mv | 10.1080/19420862.2015.1114320 |
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Monoclonal antibody INNs comprise a -mab suffix preceded by a substem indicating the antibody type, e.g., chimeric (-xi-), humanized (-zu-), or human (-u-). The WHO publishes INN definitions that specify how new monoclonal antibody therapeutics are categorized and adapts the definitions to new technologies. However, rapid progress in antibody technologies has blurred the boundaries between existing antibody categories and created a burgeoning array of new antibody formats. Thus, revising the INN system for antibodies is akin to aiming for a rapidly moving target. The WHO recently revised INN definitions for antibodies now to be based on amino acid sequence identity. These new definitions, however, are critically flawed as they are ambiguous and go against decades of scientific literature. A key concern is the imposition of an arbitrary threshold for identity against human germline antibody variable region sequences. This leads to inconsistent classification of somatically mutated human antibodies, humanized antibodies as well as antibodies derived from semi-synthetic/synthetic libraries and transgenic animals. Such sequence-based classification implies clear functional distinction between categories (e.g., immunogenicity). However, there is no scientific evidence to support this. Dialog between the WHO INN Expert Group and key stakeholders is needed to develop a new INN system for antibodies and to avoid confusion and miscommunication between researchers and clinicians prescribing antibodies.</description><identifier>ISSN: 1942-0862</identifier><identifier>EISSN: 1942-0870</identifier><identifier>DOI: 10.1080/19420862.2015.1114320</identifier><identifier>PMID: 26716992</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Animals ; Antibodies ; antibody ; BASIC BIOLOGICAL SCIENCES ; chimeric ; Complementarity Determining Region (CDR) ; definition ; framework ; humanized ; Humans ; International Immunogenetics Information System (IMGT) ; International Nonproprietary Name (INN) ; monoclonal ; Research & Experimental Medicine ; Terminology as Topic ; World Health Organization (WHO)</subject><ispartof>mAbs, 2016-01, Vol.8 (1), p.1-9</ispartof><rights>2016 The Author(s). Published with license by Taylor & Francis Group, LLC © Tim D. Jones, Paul J. Carter, Andreas Plückthun, Max Vásquez, Robert G.E. Holgate, Isidro Hötzel, Andrew G. Popplewell, Paul W.H.I. Parren, Markus Enzelberger, Hendrik J. Rademaker, Michael R. Clark, David C. Lowe, Bassil I. Dahiyat, Victoria Smith, John M. Lambert, Herren Wu, Mary Reilly, John S. Haurum, Stefan Dübel, James S. Huston, Thomas Schirrmann, Richard A.J. Janssen, Martin Steegmaier, Jane A. Gross, Andrew R.M. Bradbury, Dennis R. Burton, Dimiter S. Dimitrov, Kerry A. Chester, Martin J. Glennie, Julian Davies, Adam Walker, Steve Martin, John McCafferty, and Matthew P. Baker 2016</rights><rights>2016 The Author(s). Published with license by Taylor & Francis Group, LLC 2016 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495t-e1f9989269212da1dd4c218505cbe4ca6db0e0ef593fc1a46e63bb0fc76f26a93</citedby><cites>FETCH-LOGICAL-c495t-e1f9989269212da1dd4c218505cbe4ca6db0e0ef593fc1a46e63bb0fc76f26a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966553/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966553/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26716992$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/servlets/purl/1625100$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Jones, Tim D.</creatorcontrib><creatorcontrib>Carter, Paul J.</creatorcontrib><creatorcontrib>Plückthun, Andreas</creatorcontrib><creatorcontrib>Vásquez, Max</creatorcontrib><creatorcontrib>Holgate, Robert G.E.</creatorcontrib><creatorcontrib>Hötzel, Isidro</creatorcontrib><creatorcontrib>Popplewell, Andrew G.</creatorcontrib><creatorcontrib>Parren, Paul W.H.I.</creatorcontrib><creatorcontrib>Enzelberger, Markus</creatorcontrib><creatorcontrib>Rademaker, Hendrik J.</creatorcontrib><creatorcontrib>Clark, Michael R.</creatorcontrib><creatorcontrib>Lowe, David C.</creatorcontrib><creatorcontrib>Dahiyat, Bassil I.</creatorcontrib><creatorcontrib>Smith, Victoria</creatorcontrib><creatorcontrib>Lambert, John M.</creatorcontrib><creatorcontrib>Wu, Herren</creatorcontrib><creatorcontrib>Reilly, Mary</creatorcontrib><creatorcontrib>Haurum, John S.</creatorcontrib><creatorcontrib>Dübel, Stefan</creatorcontrib><creatorcontrib>Huston, James S.</creatorcontrib><creatorcontrib>Schirrmann, Thomas</creatorcontrib><creatorcontrib>Janssen, Richard A.J.</creatorcontrib><creatorcontrib>Steegmaier, Martin</creatorcontrib><creatorcontrib>Gross, Jane A.</creatorcontrib><creatorcontrib>Bradbury, Andrew R.M.</creatorcontrib><creatorcontrib>Burton, Dennis R.</creatorcontrib><creatorcontrib>Dimitrov, Dimiter S.</creatorcontrib><creatorcontrib>Chester, Kerry A.</creatorcontrib><creatorcontrib>Glennie, Martin J.</creatorcontrib><creatorcontrib>Davies, Julian</creatorcontrib><creatorcontrib>Walker, Adam</creatorcontrib><creatorcontrib>Martin, Steve</creatorcontrib><creatorcontrib>McCafferty, John</creatorcontrib><creatorcontrib>Baker, Matthew P.</creatorcontrib><creatorcontrib>Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)</creatorcontrib><title>The INNs and outs of antibody nonproprietary names</title><title>mAbs</title><addtitle>MAbs</addtitle><description>An important step in drug development is the assignment of an International Nonproprietary Name (INN) by the World Health Organization (WHO) that provides healthcare professionals with a unique and universally available designated name to identify each pharmaceutical substance. Monoclonal antibody INNs comprise a -mab suffix preceded by a substem indicating the antibody type, e.g., chimeric (-xi-), humanized (-zu-), or human (-u-). The WHO publishes INN definitions that specify how new monoclonal antibody therapeutics are categorized and adapts the definitions to new technologies. However, rapid progress in antibody technologies has blurred the boundaries between existing antibody categories and created a burgeoning array of new antibody formats. Thus, revising the INN system for antibodies is akin to aiming for a rapidly moving target. The WHO recently revised INN definitions for antibodies now to be based on amino acid sequence identity. These new definitions, however, are critically flawed as they are ambiguous and go against decades of scientific literature. A key concern is the imposition of an arbitrary threshold for identity against human germline antibody variable region sequences. This leads to inconsistent classification of somatically mutated human antibodies, humanized antibodies as well as antibodies derived from semi-synthetic/synthetic libraries and transgenic animals. Such sequence-based classification implies clear functional distinction between categories (e.g., immunogenicity). However, there is no scientific evidence to support this. Dialog between the WHO INN Expert Group and key stakeholders is needed to develop a new INN system for antibodies and to avoid confusion and miscommunication between researchers and clinicians prescribing antibodies.</description><subject>Animals</subject><subject>Antibodies</subject><subject>antibody</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>chimeric</subject><subject>Complementarity Determining Region (CDR)</subject><subject>definition</subject><subject>framework</subject><subject>humanized</subject><subject>Humans</subject><subject>International Immunogenetics Information System (IMGT)</subject><subject>International Nonproprietary Name (INN)</subject><subject>monoclonal</subject><subject>Research & Experimental Medicine</subject><subject>Terminology as Topic</subject><subject>World Health Organization (WHO)</subject><issn>1942-0862</issn><issn>1942-0870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><recordid>eNp9UU1P3DAQtSpQQcBPaBX1xGWXGSd24gsCIaBIiF7o2XIcu-sqsRfb24p_j6NdVu0FX-bDb948-xHyBWGJ0MEFioZCx-mSArIlIjY1hU_keO4voGvhYJ9zekTOUvoN82kBW_hMjihvkQtBjwl9Xpnq4ekpVcoPVdjkVAVb8uz6MLxWPvh1DOvoTFaxlGoy6ZQcWjUmc7aLJ-Tn3e3zzffF44_7h5vrx4VuBMsLg1aITlAuKNJB4TA0mmLHgOneNFrxoQcDxjJRW42q4YbXfQ9Wt9xSrkR9Qi63vOtNP5lBG5-jGmURMxUtMign_7_xbiV_hT-yEZwzVheCb1uCkLKTSbts9EoH743OEjllCFBA57stMbxsTMpyckmbcVTehE2S2LIayp_zGcq2UB1DStHYvRYEOfsi332Rsy9y50uZ-_rvQ_ZT7y4UwNUW4LwNcVJ_QxwHmdXrGKKNymuXZP3xjjfZ3pvN</recordid><startdate>20160102</startdate><enddate>20160102</enddate><creator>Jones, Tim D.</creator><creator>Carter, Paul J.</creator><creator>Plückthun, Andreas</creator><creator>Vásquez, Max</creator><creator>Holgate, Robert G.E.</creator><creator>Hötzel, Isidro</creator><creator>Popplewell, Andrew 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Thomas</au><au>Janssen, Richard A.J.</au><au>Steegmaier, Martin</au><au>Gross, Jane A.</au><au>Bradbury, Andrew R.M.</au><au>Burton, Dennis R.</au><au>Dimitrov, Dimiter S.</au><au>Chester, Kerry A.</au><au>Glennie, Martin J.</au><au>Davies, Julian</au><au>Walker, Adam</au><au>Martin, Steve</au><au>McCafferty, John</au><au>Baker, Matthew P.</au><aucorp>Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The INNs and outs of antibody nonproprietary names</atitle><jtitle>mAbs</jtitle><addtitle>MAbs</addtitle><date>2016-01-02</date><risdate>2016</risdate><volume>8</volume><issue>1</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>1942-0862</issn><eissn>1942-0870</eissn><abstract>An important step in drug development is the assignment of an International Nonproprietary Name (INN) by the World Health Organization (WHO) that provides healthcare professionals with a unique and universally available designated name to identify each pharmaceutical substance. Monoclonal antibody INNs comprise a -mab suffix preceded by a substem indicating the antibody type, e.g., chimeric (-xi-), humanized (-zu-), or human (-u-). The WHO publishes INN definitions that specify how new monoclonal antibody therapeutics are categorized and adapts the definitions to new technologies. However, rapid progress in antibody technologies has blurred the boundaries between existing antibody categories and created a burgeoning array of new antibody formats. Thus, revising the INN system for antibodies is akin to aiming for a rapidly moving target. The WHO recently revised INN definitions for antibodies now to be based on amino acid sequence identity. These new definitions, however, are critically flawed as they are ambiguous and go against decades of scientific literature. A key concern is the imposition of an arbitrary threshold for identity against human germline antibody variable region sequences. This leads to inconsistent classification of somatically mutated human antibodies, humanized antibodies as well as antibodies derived from semi-synthetic/synthetic libraries and transgenic animals. Such sequence-based classification implies clear functional distinction between categories (e.g., immunogenicity). However, there is no scientific evidence to support this. Dialog between the WHO INN Expert Group and key stakeholders is needed to develop a new INN system for antibodies and to avoid confusion and miscommunication between researchers and clinicians prescribing antibodies.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>26716992</pmid><doi>10.1080/19420862.2015.1114320</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies antibody BASIC BIOLOGICAL SCIENCES chimeric Complementarity Determining Region (CDR) definition framework humanized Humans International Immunogenetics Information System (IMGT) International Nonproprietary Name (INN) monoclonal Research & Experimental Medicine Terminology as Topic World Health Organization (WHO) |
title | The INNs and outs of antibody nonproprietary names |
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