Intrabodies: Turning the humoral immune system outside in for intracellular immunization

被引:79
作者
Marasco, WA [1 ]
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV INFECT DIS,BOSTON,MA 02115
关键词
antibody engineering; intracellular antibodies; gene therapy; AIDS; oncogenes;
D O I
10.1038/sj.gt.3300346
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
Antibodies have long been used in biomedical science as in vitro tools for the identification, purification and functional manipulation of target antigens; they have been exploited in vivo for diagnostic and therapeutic applications as well. Recent advances in antibody engineering have now Allowed the genes encoding antibodies to be manipulated so that the antigen binding domain can be expressed intracellularly. The specific and high-affinity binding properties of antibodies, combined with their ability to be stably expressed in precise intracellular locations inside mammalian cells, has provided a powerful new family of molecules for gene therapy applications. These intracellular antibodies are termed 'intrabodies'. Two clinical protocols have been approved by the RAC for the use of intrabodies bodies in the treatment of an oncologic and an infectious disease. Their clinical use will in all likelihood become widespread if these initial studies show 'proof in principle'. In this article, the studies from laboratories that have used intrabodies as molecular reagents for cancer therapy and for the control of infectious diseases will be reviewed and future directions of this technology will be discussed.
引用
收藏
页码:11 / 15
页数:5
相关论文
共 61 条
[31]   INTRACELLULAR INTERFERENCE OF TICK-BORNE FLAVIVIRUS INFECTION BY USING A SINGLE-CHAIN ANTIBODY FRAGMENT DELIVERED BY RECOMBINANT SINDBIS VIRUS [J].
JIANG, WR ;
VENUGOPAL, K ;
GOULD, EA .
JOURNAL OF VIROLOGY, 1995, 69 (02) :1044-1049
[32]  
JONES SD, 1995, J CELL BIO A, V21, P395
[33]  
JOST CR, 1994, J BIOL CHEM, V269, P26267
[34]  
LEVIN R, 1996, IN PRESS MOL MED
[35]   ANTIGEN-SPECIFIC HUMAN-ANTIBODIES FROM MICE COMPRISING 4 DISTINCT GENETIC MODIFICATIONS [J].
LONBERG, N ;
TAYLOR, LD ;
HARDING, FA ;
TROUNSTINE, M ;
HIGGINS, KM ;
SCHRAMM, SR ;
KUO, CC ;
MASHAYEKH, R ;
WYMORE, K ;
MCCABE, JG ;
MUNOZOREGAN, D ;
ODONNELL, SL ;
LAPACHET, ESG ;
BENGOECHEA, T ;
FISHWILD, DM ;
CARMACK, CE ;
KAY, RM ;
HUSZAR, D .
NATURE, 1994, 368 (6474) :856-859
[36]   INTRACELLULAR EXPRESSION OF ANTIBODY FRAGMENTS DIRECTED AGAINST HIV REVERSE-TRANSCRIPTASE PREVENTS HIV-INFECTION IN-VITRO [J].
MACIEJEWSKI, JP ;
WEICHOLD, FF ;
YOUNG, NS ;
CARA, A ;
ZELLA, D ;
REITZ, MS ;
GALLO, RC .
NATURE MEDICINE, 1995, 1 (07) :667-673
[37]   INTRACELLULAR ANTIBODIES (INTRABODIES) AS RESEARCH REAGENTS AND THERAPEUTIC MOLECULES FOR GENE-THERAPY [J].
MARASCO, WA .
IMMUNOTECHNOLOGY, 1995, 1 (01) :1-19
[38]   DESIGN, INTRACELLULAR EXPRESSION, AND ACTIVITY OF A HUMAN ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 GP120 SINGLE-CHAIN ANTIBODY [J].
MARASCO, WA ;
HASELTINE, WA ;
CHEN, SY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7889-7893
[39]  
MARASCO WA, 1996, INT S INT CTR GEN EN
[40]   Phage libraries - A new route to clinically useful antibodies [J].
Marks, C ;
Marks, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (10) :730-733