NKT and MAIT invariant TCRα sequences can be produced efficiently by VJ gene recombination

Immunobiology

Volumn 218, Issue 2, 2013, Pages 213-224

  Greenaway, Hui Yee ^a   Ng, Benedict ^a   Price, David A ^b,c   Douek, Daniel C ^c   Davenport, Miles P ^a   Venturi, Vanessa ^a  

^a UNIVERSITY OF NEW SOUTH WALES   (Australia)

^b CARDIFF UNIVERSITY SCHOOL OF MEDICINE   (United Kingdom)

^c NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

Author keywords

Invariant T cell receptor; MAIT cell; NKT cell; Public T cell response; T cell receptor; T cell repertoire

Indexed keywords

T LYMPHOCYTE RECEPTOR ALPHA CHAIN;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; GENE; GENE IDENTIFICATION; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; HUMAN VERSUS NONHUMAN DATA; MOLECULAR DYNAMICS; MOUSE; MUCOSAL ASSOCIATED INVARIANT T CELL; NATURAL KILLER T CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION; SEQUENCE ANALYSIS; T LYMPHOCYTE; TRAJ GENE; TRAJ18 GENE; TRAV GENE; TRAV10 GENE; TRAV11 GENE;

ANIMALS; BASE SEQUENCE; BIOLOGICAL EVOLUTION; CATTLE; DOGS; GENE REARRANGEMENT, T-LYMPHOCYTE; GENES, T-CELL RECEPTOR ALPHA; HUMANS; IMMUNITY, INNATE; MACACA MULATTA; MICE; MUCOUS MEMBRANE; NATURAL KILLER T-CELLS; RATS; SEQUENCE ALIGNMENT; SWINE; V(D)J RECOMBINATION;

EID: 84871921179     PISSN: 01712985     EISSN: 18783279     Source Type: Journal    
DOI: 10.1016/j.imbio.2012.04.003     Document Type: Article

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