IMGT/HighV QUEST paradigm for T cell receptor IMGT clonotype diversity and next generation repertoire immunoprofiling

Autor: Vincent Corbin, Bruce E. Loveland, Marie-Paule Lefranc, Eric J. Gowans, Anthony T. Papenfuss, Paul U. Cameron, Jean-Pierre Y. Scheerlinck, Magdalena Plebanski, Michael A. Frohman, J. Douglas Freeman, Patrice Duroux, Scott R. Burrows, Véronique Giudicelli, John J. Miles, Shuo Li, Eltaf Alamyar
Přispěvatelé: Department of Microbiolgy and Immunology, School of Biomedical Sciences [Melbourne], Faculty of Medicine, Dentistry and Health Sciences [Melbourne], University of Melbourne-University of Melbourne-Faculty of Medicine, Dentistry and Health Sciences [Melbourne], University of Melbourne-University of Melbourne, Institut de génétique humaine (IGH), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2013
Předmět:
Zdroj: Nature Communications
Nature Communications, Nature Publishing Group, 2013, 4, pp.2333. ⟨10.1038/ncomms3333⟩
ISSN: 2041-1723
DOI: 10.1038/ncomms3333⟩
Popis: T cell repertoire diversity and clonotype follow-up in vaccination, cancer, infectious and immune diseases represent a major challenge owing to the enormous complexity of the data generated. Here we describe a next generation methodology, which combines 5′RACE PCR, 454 sequencing and, for analysis, IMGT, the international ImMunoGeneTics information system (IMGT), IMGT/HighV-QUEST web portal and IMGT-ONTOLOGY concepts. The approach is validated in a human case study of T cell receptor beta (TRB) repertoire, by chronologically tracking the effects of influenza vaccination on conventional and regulatory T cell subpopulations. The IMGT/HighV-QUEST paradigm defines standards for genotype/haplotype analysis and characterization of IMGT clonotypes for clonal diversity and expression and achieves a degree of resolution for next generation sequencing verifiable by the user at the sequence level, while providing a normalized reference immunoprofile for human TRB.
Dynamic changes in T cell repertoire underlie immune responses during infection, allergy, autoimmunity and cancer. Here, Li et al. present a workflow for high throughput sequencing and analysis of T cell receptor sequences, and use it to monitor the T cell response to influenza vaccination in a human patient.
Databáze: OpenAIRE