Potent antitumour activity of a new class of tumour-specific killer cells

被引:61
作者
Chen, SY
Yang, AG
Chen, JD
Kute, T
King, CR
Collier, J
Cong, YP
Yao, CP
Huang, XF
机构
[1] WAKE FOREST UNIV,BOWMAN GRAY SCH MED,CTR COMPREHENS CANC,DEPT PATHOL,WINSTON SALEM,NC 27157
[2] WAKE FOREST UNIV,BOWMAN GRAY SCH MED,CTR COMPREHENS CANC,DEPT COMPARAT MED,WINSTON SALEM,NC 27157
[3] GEORGETOWN UNIV,VINCENT T LOMBARDI CANC RES CTR,DEPT BIOCHEM,WASHINGTON,DC 20007
[4] HARVARD UNIV,SCH MED,DEPT MICROBIOL & MOL GENET,BOSTON,MA 02115
关键词
D O I
10.1038/385078a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Two approaches to the antibody-directed targeting of toxic or cytolytic activity and augmentation of cellular immune responses have been explored For tumour immunotherapy, but so far success has been limited(1-3). Obstacles facing immunotherapy are the limited accessibility of antibodies or antibody conjugates to solid tumours and the difficulty in obtaining tumour-specific cytotoxic lymphocytes(4-7). Here we generate a new class of tumour-specific killer cells by genetically modifying lymphocytes to produce and secrete a targeted toxin against an oncoprotein overexpressed on breast and other tumour cells, The transduced lymphocytes were shown to have potent and selective cytotoxicity to tumours in culture and nude mouse models, The potent in vivo antitunour activity is probably a result of the migration of the lymphocytes to tumours as a targeted toxin carrier, and production and accumulation of the targeted toxins inside tumours as a producer. Our approach, which has features of both antibody-directed and cell-mediated immunotherapy, may have application in a gene therapy context.
引用
收藏
页码:78 / 80
页数:3
相关论文
共 27 条
[1]   RECOMBINANT ANTI-ERBB2 IMMUNOTOXINS CONTAINING PSEUDOMONAS EXOTOXIN [J].
BATRA, JK ;
KASPRZYK, PG ;
BIRD, RE ;
PASTAN, I ;
KING, CR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :5867-5871
[2]  
CHEN SY, 1995, GENE THER, V2, P116
[3]   COMBINED INTRACELLULAR AND EXTRACELLULAR IMMUNIZATION AGAINST HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION WITH A HUMAN ANTI-GP120 ANTIBODY [J].
CHEN, SY ;
KHOURI, Y ;
BAGLEY, J ;
MARASCO, WA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (13) :5932-5936
[4]  
COLLIER RJ, 1971, J BIOL CHEM, V246, P1496
[5]   LYMPHOCYTES AS CELLULAR VEHICLES FOR GENE-THERAPY IN MOUSE AND MAN [J].
CULVER, K ;
CORNETTA, K ;
MORGAN, R ;
MORECKI, S ;
AEBERSOLD, P ;
KASID, A ;
LOTZE, M ;
ROSENBERG, SA ;
ANDERSON, WF ;
BLAESE, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (08) :3155-3159
[6]   ERBB-2 IS A POTENT ONCOGENE WHEN OVEREXPRESSED IN NIH/3T3 CELLS [J].
DIFIORE, PP ;
PIERCE, JH ;
KRAUS, MH ;
SEGATTO, O ;
KING, CR ;
AARONSON, SA .
SCIENCE, 1987, 237 (4811) :178-182
[7]   EXPRESSION OF IMMUNOGLOBULIN-T-CELL RECEPTOR CHIMERIC MOLECULES AS FUNCTIONAL RECEPTORS WITH ANTIBODY-TYPE SPECIFICITY [J].
GROSS, G ;
WAKS, T ;
ESHHAR, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :10024-10028
[8]   FUNCTIONAL DOMAINS OF PSEUDOMONAS EXOTOXIN IDENTIFIED BY DELETION ANALYSIS OF THE GENE EXPRESSED IN ESCHERICHIA-COLI [J].
HWANG, J ;
FITZGERALD, DJ ;
ADHYA, S ;
PASTAN, I .
CELL, 1987, 48 (01) :129-136
[9]   BARRIERS TO DRUG-DELIVERY IN SOLID TUMORS [J].
JAIN, RK .
SCIENTIFIC AMERICAN, 1994, 271 (01) :58-65
[10]  
JOHNSON RA, 1982, APPLIED MULTIVARIATE, P226