Nomenclature of monoclonal antibodies


The nomenclature of monoclonal antibodies is a naming scheme for assigning generic, or nonproprietary, names to monoclonal antibodies. An antibody is a protein that is produced in B cells and used by the immune system of humans and other vertebrate animals to identify a specific foreign object like a bacterium or a virus. Monoclonal antibodies are those that were produced in identical cells, often artificially, and so share the same target object. They have a wide range of applications including medical uses.
This naming scheme is used for both the World Health Organization’s International Nonproprietary Names and the United States Adopted Names for pharmaceuticals. In general, word stems are used to identify classes of drugs, in most cases placed word-finally. All monoclonal antibody names end with the stem -mab. Unlike most other pharmaceuticals, monoclonal antibody nomenclature uses different preceding word parts depending on structure and function. These are officially called substems and sometimes erroneously infixes, even by the USAN Council itself.

Components

Stem

The stem -mab is used for monoclonal antibodies as well as for their fragments, as long as at least one variable domain is included. This is the case for antigen-binding fragments and single-chain variable fragments, among other artificial proteins. Other antibody parts and antibody mimetics use different naming schemes.

Substem for origin/source

In April 2017, at the WHO's 64th Consultation on International Nonproprietary Names for Pharmaceutical Substances, it was decided to drop the source substem and from that meeting onwards, it is no longer used in new antibody names.
The substem preceding the stem denoted the animal from which the antibody was obtained. The first monoclonal antibodies were produced in mice or other non-human organisms. Neither INN nor USAN has ever been requested for antibodies from rats, hamsters and primates.
These non-human antibodies are recognized as foreign by the human immune system and may be rapidly cleared from the body, provoke an allergic reaction, or both. To avoid this, parts of the antibody can be replaced with human amino acid sequences, or pure human antibodies can be engineered. If the constant region is replaced with the human form, the antibody is termed chimeric and the substem used was -xi-. Part of the variable regions may also be substituted, in which case it is called humanized and -zu- was used; typically, everything is replaced except the complementarity-determining regions, the three loops of amino acid sequences at the outside of each variable region that bind to the target structure, although some other residues may have to remain non-human in order to achieve good binding. Partly chimeric and partly humanized antibodies used -xizu-. These three substems did not indicate the foreign species used for production. Thus, the human/mouse chimeric antibody basiliximab ends in -ximab just as does the human/macaque antibody gomiliximab. Purely human antibodies used -u-.
Rat/mouse hybrid antibodies can be engineered with binding sites for two different antigens. These drugs, termed trifunctional antibodies, had the substem -axo-.
The difficulty in capturing the complexity and subtleties of the many methods by which antibody drugs can be produced is one of the reasons that the INN dropped the source substem.

Substem for target

The substem preceding the source of the antibody refers to the medicine's target. Examples of targets are tumors, organ systems like the circulatory system, or infectious agents like bacteria or viruses. The term target does not imply what sort of action the antibody exerts. Therapeutic, prophylactic and diagnostic agents are not distinguished by this nomenclature.
In the naming scheme as originally developed, these substems mostly consist of a consonant, a vowel, then another consonant. The final letter may be dropped if the resulting name would be difficult to pronounce otherwise. Examples include -ci- for the circulatory system, -li- for the immune system and -ne- for the nervous system. The final letter is usually omitted if the following source substem begins with a consonant, but not all target substems are used in their shortened form. -mul-, for example, is never reduced to -mu- because no chimeric or humanized antibodies targeting the musculoskeletal system ever received an INN. Combination of target and source substems results in endings like -limumab or -ciximab.
New and shorter target substems were adopted in 2009. They mostly consist of a consonant, plus a vowel which is omitted if the source substem begins with a vowel. For example, human antibodies targeting the immune system receive names ending in -lumab instead of the old -limumab. Some endings like -ciximab remain unchanged. The old system employed seven different substems for tumor targets, depending on the type of tumor. Because many antibodies are investigated for several tumor types, the new convention only has -t-.

Prefix

The prefix carries no special meaning. It should be unique for each medicine and contribute to a well-sounding name. This means that antibodies with the same source and target substems are only distinguished by their prefix. Even antibodies targeting exactly the same structure are differently prefixed, such as the adalimumab and golimumab, both of which are TNF inhibitors but differ in their chemical structure.

Additional words

A second word following the name of the antibody indicates that another substance is attached, which is done for several reasons.
and Kitasato Shibasaburō discovered in 1890 that diphtheria and tetanus toxins were neutralized in the bloodstream of animals by substances they called antitoxins, which were specific for the respective toxin. Behring received the first Nobel Prize in Physiology or Medicine for their find in 1901. A year after the discovery, Paul Ehrlich used the term antibodies for these antitoxins.
The principle of monoclonal antibody production, called hybridoma technology, was published in 1975 by Georges Köhler and César Milstein, who were awarded the 1984 Medicine Nobel Prize for their discovery together with Niels Kaj Jerne. Muromonab-CD3 was the first monoclonal antibody to be approved for clinical use in humans, in 1986.
The World Health Organization introduced the system of International Nonproprietary Names in 1950, with the first INN list being published three years later. The stem -mab for monoclonal antibodies was proposed around 1990, and the current system with target and source substems was developed between 1991 and 1993. Due to the collaboration between the WHO and the United States Adopted Names Council, antibody USANs have the same structure and are largely identical to INNs. Until 2009, more than 170 monoclonal antibodies received names following this nomenclature.
In October 2008, the WHO convoked a working group to revise the nomenclature of monoclonal antibodies, to meet challenges discussed in April the same year. This led to the adoption of the new target substems in November 2009. In spring 2010, the first new antibody names were adopted.

Examples

New convention