The INNs and outs of antibody nonproprietary names. Issue 1 (2nd January 2016)
- Record Type:
- Journal Article
- Title:
- The INNs and outs of antibody nonproprietary names. Issue 1 (2nd January 2016)
- Main Title:
- The INNs and outs of antibody nonproprietary names
- Authors:
- 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.
… (more) - Abstract:
- 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 betweenAbstract : 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. … (more)
- Is Part Of:
- MAbs. Volume 8:Issue 1(2016)
- Journal:
- MAbs
- Issue:
- Volume 8:Issue 1(2016)
- Issue Display:
- Volume 8, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 8
- Issue:
- 1
- Issue Sort Value:
- 2016-0008-0001-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2016-01-02
- Subjects:
- antibody -- chimeric -- Complementarity Determining Region (CDR) -- definition -- framework -- humanized -- International Nonproprietary Name (INN) -- International Immunogenetics Information System (IMGT) -- monoclonal -- World Health Organization (WHO)
Monoclonal antibodies -- Therapeutic use -- Periodicals
Monoclonal antibodies -- Periodicals
Antibodies, Monoclonal -- Periodicals
616.0798 - Journal URLs:
- http://www.tandfonline.com/loi/kmab20#.VufTUVLcuic ↗
http://www.landesbioscience.com/journals/mabs ↗
http://www.tandfonline.com/ ↗ - DOI:
- 10.1080/19420862.2015.1114320 ↗
- Languages:
- English
- ISSNs:
- 1942-0862
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5320.243000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5278.xml