Felix Breden (Canada), 2013
John Hammond (UK), 2020
- Eva Bengtén (USA) 2006
- Salvatrice Ciccarese (Italy) 2007
- Deborah Dunn‐Walters (UK) 2006
- Jean‐Pol Frippiat (France) 2006
- Véronique Giudicelli (France) 2014
- Sofia Kossida (France) 2014
- Ramit Mehr (Israel) 2017
- Serge Muyldermans (Belgium) 2006
- John Schwartz (UK) 2020
- Jamie Scott (Canada) 2013
- Corey T. Watson (USA) 2013
The IG/TR/MH Sub-committee adopted Terms of Reference in Spring 2022 outlining a democratic and transparent governance structure. The following description of the Sub-committee’s goals, structure, and processes will be revised over the next several months as it responds to changes in the quantity and types of data available for understanding IG and TR germline gene polymorphisms, and as the Sub-committee strives to best serve the immunogenetics community.
In continuing the pioneering work of Dr. Marie-Paule Lefranc, the IG/TR/MH Nomenclature Sub-committee is responsible for validating, approving, and assigning names to newly discovered immunoglobulin (IG) and T-cell receptor (TR) germline genes and non-human MHC genes (MH), following the principles of the IMGT™ information system insofar as possible. This Sub-committee is also responsible for coordinating the biocuration of these genes in the appropriate germline gene databases.
The IG/TR/MH Nomenclature Sub-committee will practice in its governance and its partnerships:
- Excellence and professionalism
- Inclusivity and diversity
- Transparency and integrity
- Innovation and sustainability
Terms of Reference
Click here to access the terms of reference for this Sub-committee
Reports to IUIS.
You will find information about the history of the Sub-Committee since its creation and annual reports through the 17th International Congress of Immunology in 2019 here:
TR-IG Review Committee (formerly IMGT-NC Reports Review Committee)
The TR-IG Review Committee was established by the IUIS IG/TR/MH Nomenclature Sub-Committee. It evaluates, names, and reports new germline genes encoding immunoglobulins (IG) and T-cell receptors (TR). This function was previously performed by the IMGT-NC Reports Review Committee, which was replaced by an elected body in October 2022 and was renamed as the TR-IG Review Committee in March 2023. TR-IG has been tasked with developing methods and procedures for reviewing new TR and IG genes for inclusion in databases.
Andrew Collins (University of New South Wales; webpage) 2022
Elisa Rosati Scalchi (GSK; Linkedin) 2022
Corey Watson (University of Louisville; webpage) 2022
Henk-Jan van den Ham (ENPICOM;LinkedIn) 2022
Luc Teyton (Scripps Research; webpage) 2022
Yana Safonova (Johns Hopkins; webpage) 2022
To contact Nomenclature TR-IG Review Committee, please send an email to: email@example.com and mention “Attention TR-IG Review Committee” in the subject line.
To contact TR-IG Subcommittee, please send an email to: firstname.lastname@example.org
Germline gene submission for review and approval:
Scientists submit sequences for new IG and TR variable (V), diversity (D), joining (J) and constant (C) genes and alleles to the TR-IG Review Committee. Working with the submitters, members of this Review Committee review and approve sequences and names, based on specific data-driven criteria and review processes. Validated IG and TR germline gene sequences and their names are passed to partner databases for curation and inclusion in germline gene/allele sets.
Note: The appropriate procedures and submission forms are currently being developed. Please contact us if you would like to submit sequences for review and approval.
Click here for a description of the current submission procedure.
Inferred Allele Review Committee
IG and TR germline V gene sequences can also be deduced from next-generation sequencing data from a B- or T-cell receptor repertoire. The Inferred Allele Review Committee (IARC) is a committee of the Adaptive Immune Receptor Repertoire (AIRR) Community Committee of The Antibody Society whose mission is to validate human IG and TR germline V gene allelic sequences that have been inferred from next-generation sequencing data. Criteria required for an inferred V allele to be considered for validation include (1) deposition of the repertoire from which the inference was made in the NCBI or ENA and in a peer-reviewed publication, (2) the complete V coding region, (3) inferences made with a validated and publicly available tool published in a peer-reviewed publication. Working with the IMGT-NC Reports Review Committee, validated gene sequences are named and added to the IMGT-NC Report.
Guidelines for submitting inferred allele sequences to the IARC can be found here.
Mats Ohlin (Sweden), Chair
Current public databases containing IG and TR germline-gene sequences and reference sets.