Engineered T cell receptors and their potential in molecular medicine

被引:16
作者
Miles, John J.
Silins, Sharon L.
Burrows, Scott R. [1 ]
机构
[1] Queensland Inst Med Res, Cellular Immunol Lab, Herston, Qld 4029, Australia
[2] Univ Queensland, Sch Populat Hlth, Herston, Qld 4029, Australia
关键词
T cell receptor; immunotherapy; major histocompatibility complex; human leucocyte antigens;
D O I
10.2174/092986706778521959
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
T cell receptors are among the most specific biological structures found in nature and are therefore excellent candidates for the molecular targeting of antigen. It is becoming increasingly apparent that common sets of T cell receptors are frequently used in humans to combat pathogen and cancer derived threats. Given that many of these conserved T cell receptors have high affinity for their target ligands, there is potential to amass virtual banks of "off-the-shelf" receptors for use in a wide range of immunotherapeutic strategies. Additionally, such T cell receptors could become basic blueprints for artificial enhancement through mutagenesis, thereby creating an even better 3-dimensional fit for their cognate targets. Indeed, preliminary approaches using both "natural" and "supernatural" T cell receptors have shown promise in treating autoimmunity and malignancy. This review will discuss these studies and other approaches through which T cell receptors can be exploited in immunodiagnostics, pathogen control and gene therapy.
引用
收藏
页码:2725 / 2736
页数:12
相关论文
共 166 条
  • [1] Andersen MH, 2001, CANCER RES, V61, P5964
  • [2] Changing patterns of dominant TCR usage with maturation of an EBV-specific cytotoxic T cell response
    Annels, NE
    Callan, MFC
    Tan, L
    Rickinson, AB
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 165 (09) : 4831 - 4841
  • [3] DOMINANT SELECTION OF AN INVARIANT T-CELL ANTIGEN RECEPTOR IN RESPONSE TO PERSISTENT INFECTION BY EPSTEIN-BARR-VIRUS
    ARGAET, VP
    SCHMIDT, CW
    BURROWS, SR
    SILINS, SL
    KURILLA, MG
    DOOLAN, DL
    SUHRBIER, A
    MOSS, DJ
    KIEFF, E
    SCULLEY, TB
    MISKO, IS
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (06) : 2335 - 2340
  • [4] A direct estimate of the human αβ T cell receptor diversity
    Arstila, TP
    Casrouge, A
    Baron, V
    Even, J
    Kanellopoulos, J
    Kourilsky, P
    [J]. SCIENCE, 1999, 286 (5441) : 958 - 961
  • [5] Identification of a crucial energetic footprint on the al helix of human histocompatibility leukocyte antigen (HLA)-A2 that provides functional interactions for recognition by tax peptide/HLA-A2-specifrc T cell receptors
    Baker, BM
    Turner, RV
    Gagnon, SJ
    Wiley, DC
    Biddison, WE
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (05) : 551 - 562
  • [6] Two distinct HLA-A0201-presented epitopes of the Wilms tumor antigen can function as targets for leukemia-reactive CTL
    Bellantuono, I
    Gao, LQ
    Parry, S
    Marley, S
    Dazzi, F
    Apperley, J
    Goldman, JM
    Stauss, HJ
    [J]. BLOOD, 2002, 100 (10) : 3835 - 3837
  • [7] BESTER AC, 2006, GENE THER
  • [8] Safety of retroviral gene marking with a truncated NGF receptor
    Bonini, C
    Grez, M
    Traversari, C
    Ciceri, F
    Marktel, S
    Ferrari, G
    Dinauer, M
    Sadat, M
    Aiuti, A
    Deola, S
    Radrizzani, M
    Hagenbeek, A
    Apperley, J
    Ebeling, S
    Martens, A
    Kolb, HJ
    Weber, M
    Lotti, F
    Grande, A
    Weissinger, E
    Bueren, JA
    Lamana, M
    Falkenburg, JHF
    Heemskerk, MHM
    Austin, T
    Kornblau, S
    Marini, F
    Benati, C
    Magnani, Z
    Cazzaniga, S
    Toma, S
    Gallo-Stampino, C
    Introna, M
    Slavin, S
    Greenberg, PD
    Bregni, M
    Mavilio, F
    Bordignon, C
    [J]. NATURE MEDICINE, 2003, 9 (04) : 367 - 369
  • [9] HSV-TK gene transfer into donor lymphocytes for control of allogeneic graft-versus-leukemia
    Bonini, C
    Ferrari, G
    Verzeletti, S
    Servida, P
    Zappone, E
    Ruggieri, L
    Ponzoni, M
    Rossini, S
    Mavilio, F
    Traversari, C
    Bordignon, C
    [J]. SCIENCE, 1997, 276 (5319) : 1719 - 1724
  • [10] The CDR3 regions of an immunodominant T cell receptor dictate the 'energetic landscape' of peptide-MHC recognition
    Borg, NA
    Ely, LK
    Beddoe, T
    Macdonald, WA
    Reid, HH
    Clements, CS
    Purcell, AW
    Kjer-Nielsen, L
    Miles, JJ
    Burrows, SR
    McCluskey, J
    Rossjohn, J
    [J]. NATURE IMMUNOLOGY, 2005, 6 (02) : 171 - 180