Frequency patterns of T-cell exposed amino acid motifs in immunoglobulin heavy chain peptides presented by MHCs

被引:25
|
作者
Bremel, Robert D. [1 ]
Homan, E. Jane [1 ]
机构
[1] EigenBio LLC, Madison, WI 53704 USA
来源
FRONTIERS IN IMMUNOLOGY | 2014年 / 5卷
关键词
T-cell biology; regulatoryT-cell; bioinformatics; B-cell:T-cell cooperation; polyspecificity; memory; ORIGINAL ANTIGENIC SIN; CUTTING EDGE; SPECIFICITY; LYMPHOCYTES; REPERTOIRE; ACTIVATION; RESPONSES; RECEPTOR; DRIVEN; RECONSTITUTION;
D O I
10.3389/fimmu.2014.00541
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
lmmunoglobulins are highly diverse protein sequences that are processed and presented to T-cells by B-cells and other antigen presenting cells. We examined a large dataset of immunoglobulin heavy chain variable regions (IGHV) to assess the diversity of T-cell exposed motifs (TCEMs). TCEM comprise those amino acids in a MHC-bound peptide, which face outwards, surrounded by the MHC histotope, and which engage the T-cell receptor. Within IGHV there is a distinct pattern of predicted MHC class II binding and a very high frequency of re-use of the TCEMs. The re-use frequency indicates that only a limited number of different cognate T-cells are required to engage many different clonal B-cells. The amino acids in each outward-facing TCEM are intercalated with the amino acids of inward-facing MHC groove-exposed motifs (GEM). Different GEM may have differing, allele-specific, MHC binding affinities. The intercalation of TCEM and GEM in a peptide allows for a vast combinatorial repertoire of epitopes, each eliciting a different response. Outcome of T-cell receptor binding is determined by overall signal strength, which is a function of the number of responding T-cells and the duration of engagement. Hence, the frequency of TCEM re-use appears to be an important determinant of whether a T-cell response is stimulatory or suppressive. The frequency distribution of TCEMs implies that somatic hypermutation is followed by T-cell clonal expansion that develops along repeated pathways. The observations of TCEM and GEM derived from immunoglobulins suggest a relatively simple, yet powerful, mechanism to correlate T-cell polyspecificity, through re-use of TCEMs, with a very high degree of specificity achieved by combination with a diversity of GEMs. The frequency profile of TCEMs also points to an economical mechanism for maintaining T-cell memory, recall, and self-discrimination based on an endogenously generated profile of motifs.
引用
收藏
页数:14
相关论文
共 50 条
  • [31] Shared amino acid motifs in T-cell receptor beta junctional regions of bronchoalveolar T cells in patients with pulmonary sarcoidosis
    Usui, Y
    Kohsaka, H
    Eishi, Y
    Saito, I
    Marumo, F
    Miyasaka, N
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (01) : 50 - 56
  • [32] T cell cross-reactivity to heavy metals:: identical cryptic peptides may be presented from protein exposed to different metals
    Griem, P
    von Vultée, C
    Panthel, K
    Best, SL
    Sadler, PJ
    Shaw, CF
    EUROPEAN JOURNAL OF IMMUNOLOGY, 1998, 28 (06) : 1941 - 1947
  • [33] ASSOCIATION OF MEMBRANOUS NEPHROPATHY WITH T-CELL RECEPTOR CONSTANT BETA-CHAIN AND IMMUNOGLOBULIN HEAVY-CHAIN SWITCH REGION POLYMORPHISMS
    DEMAINE, AG
    VAUGHAN, RW
    TAUBE, DH
    WELSH, KI
    IMMUNOGENETICS, 1988, 27 (01) : 19 - 23
  • [34] INSIGHTS ON THE AMINO-ACID SIDE-CHAIN INTERACTIONS OF A SYNTHETIC T-CELL DETERMINANT
    BORRASCUESTA, F
    GOLVANO, J
    SAROBE, P
    LASARTE, JJ
    PRIETO, I
    SZABO, A
    GUILLAUME, JL
    GUILLET, JG
    BIOLOGICALS, 1991, 19 (03) : 187 - 190
  • [35] DETECTION OF REARRANGEMENT OF IMMUNOGLOBULIN HEAVY-CHAIN AND T-CELL RECEPTOR BETA CHAIN IN LEUKEMIC-CELLS BY RESTRICTED POLYMERASE CHAIN-REACTION
    STOLC, V
    UHRMACHER, J
    KRAUSE, JR
    AMERICAN JOURNAL OF HEMATOLOGY, 1991, 38 (01) : 1 - 8
  • [36] Landscape of immunoglobulin heavy chain γ gene class switch recombination in patients with adult T-cell leukemia-lymphoma
    Hiramatsu, Hiroaki
    Nosaka, Kisato
    Kusumoto, Shigeru
    Nakano, Nobuaki
    Choi, Ilseung
    Yoshimitsu, Makoto
    Imaizumi, Yoshitaka
    Hidaka, Michihiro
    Sasaki, Hidenori
    Makiyama, Junya
    Ohtsuka, Eiichi
    Jo, Tatsuro
    Ogata, Masao
    Ito, Asahi
    Yonekura, Kentaro
    Tatetsu, Hiro
    Kato, Takeharu
    Kawakita, Toshiro
    Suehiro, Youko
    Ishitsuka, Kenji
    Iida, Shinsuke
    Matsutani, Takaji
    Nishikawa, Hiroyoshi
    Utsunomiya, Atae
    Ueda, Ryuzo
    Ishida, Takashi
    HAEMATOLOGICA, 2023, 108 (04) : 1173 - 1178
  • [37] Oligoclonal immunoglobulin heavy-chain and T-cell receptor δ rearrangements persist in a recurrent acute lymphoblastic leukemia with one immunoglobulin κ rearrangement as a clonal marker
    Stolz, F
    Panzer, S
    Fischer, S
    Panzer-Grümayer, ER
    MODERN PATHOLOGY, 1999, 12 (08) : 819 - 826
  • [38] LINEAGE SPECIFICITY OF REARRANGEMENT AND EXPRESSION OF GENES ENCODING THE T-CELL RECEPTOR-T-3 COMPLEX AND IMMUNOGLOBULIN HEAVY-CHAIN IN LEUKEMIA
    FURLEY, AJW
    CHAN, LC
    MIZUTANI, S
    FORD, AM
    WEILBAECHER, K
    PEGRAM, SM
    GREAVES, MF
    LEUKEMIA, 1987, 1 (09) : 644 - 652
  • [39] Evaluation of T-cell responses to peptides and lipopeptides with MHC class I binding motifs derived from the amino acid sequence of the19-kDa lipoprotein of Mycobacterium tuberculosis
    Fonseca, DPAJ
    Joosten, D
    Snippe, H
    Verheul, AFM
    MOLECULAR IMMUNOLOGY, 2000, 37 (08) : 413 - 422
  • [40] Determinants of tumor immune evasion: the role of T cell exposed motif frequency and mutant amino acid exposure
    Homan, E. Jane
    Bremel, Robert D.
    FRONTIERS IN IMMUNOLOGY, 2023, 14