Codon modification of T cell receptors allows enhanced functional expression in transgenic human T cells

被引:133
作者
Scholten, KBJ
Kramer, D
Kueter, EWM
Graf, M
Schoedl, T
Meijer, CJLM
Schreurs, MWJ
Hooijberg, E
机构
[1] Free Univ Amsterdam, Med Ctr, Dept Pathol, NL-1081 HV Amsterdam, Netherlands
[2] GENEART GmbH, D-93053 Regensburg, Germany
关键词
immunotherapy; retroviral transduction; T cell receptor; codon-modification; 2A peptide; HPV; gene therapy; adoptive transfer; codon optimization;
D O I
10.1016/j.clim.2005.12.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Expression of native transgenic T cell receptors in recipient human T cells is often insufficient to achieve highly reactive T cell bulks. Here we show that codon modification of an HPV16E7-specific T cell receptor (TCR), together with omission of mRNA instability motifs and (cryptic) splice sites, leads to a dramatic increase in the expression levels of the transgenic TCRs in human CD8+ T cells. The codon-modified TCRs have been tested in three different configurations in the retroviral vector LZRS: (1) TCR alpha-IRES-GFP in combination with TCR beta-IRES-NGFR, (2) TCR alpha-IRES-TCRI, and (3) TCR alpha-2A-TCR beta. T cells carrying the codon-modified TCRs are functionally active against target cells loaded with relevant peptide, model tumor cells expressing the specific epitope as well as cervical carcinoma cells. The significant improvements we report here in the functional expression of specific human TCRs wilt hopefully expedite clinical application of TCR transfer-based immunotherapy. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:135 / 145
页数:11
相关论文
共 54 条
[1]  
Calogero A, 2000, ANTICANCER RES, V20, P1793
[2]   REGULATION BY HIV REV DEPENDS UPON RECOGNITION OF SPLICE SITES [J].
CHANG, DD ;
SHARP, PA .
CELL, 1989, 59 (05) :789-795
[3]  
CHEN CYA, 1995, MOL CELL BIOL, V15, P5777
[4]  
Clay TM, 1999, J IMMUNOL, V163, P507
[5]   Transfer of specificity for human immunodeficiency virus type 1 into primary human T lymphocytes by introduction of T-cell receptor genes [J].
Cooper, LJN ;
Kalos, M ;
Lewinsohn, DA ;
Riddell, SR ;
Greenberg, PD .
JOURNAL OF VIROLOGY, 2000, 74 (17) :8207-8212
[6]   Contributions of viral splice sites and cis-regulatory elements to lentivirus vector function [J].
Cui, Y ;
Iwakuma, T ;
Chang, LJ .
JOURNAL OF VIROLOGY, 1999, 73 (07) :6171-6176
[7]   TRANSFER OF SPECIFICITY BY MURINE ALPHA-T-CELL AND BETA-T-CELL RECEPTOR GENES [J].
DEMBIC, Z ;
HAAS, W ;
WEISS, S ;
MCCUBREY, J ;
KIEFER, H ;
VONBOEHMER, H ;
STEINMETZ, M .
NATURE, 1986, 320 (6059) :232-238
[8]   An activated 5′ cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id) [J].
Denecke, J ;
Kranz, C ;
Kemming, D ;
Koch, HG ;
Marquardt, T .
HUMAN MUTATION, 2004, 23 (05) :477-486
[9]   The 'cleavage' activities of foot-and-mouth disease virus 2A site-directed mutants and naturally occurring '2A-like' sequences [J].
Donnelly, MLL ;
Hughes, LE ;
Luke, G ;
Mendoza, H ;
ten Dam, E ;
Gani, D ;
Ryan, MD .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :1027-1041
[10]   Analysis of the aphthovirus 2A/2B polyprotein 'cleavage' mechanism indicates not a proteolytic reaction, but a novel translational effect: a putative ribosomal 'skip' [J].
Donnelly, MLL ;
Luke, G ;
Mehrotra, A ;
Li, XJ ;
Hughes, LE ;
Gani, D ;
Ryan, MD .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :1013-1025