TRANSGENIC MICE EXPRESSING HUMAN TUMOR-NECROSIS-FACTOR - A PREDICTIVE GENETIC MODEL OF ARTHRITIS

被引:1332
作者
KEFFER, J
PROBERT, L
CAZLARIS, H
GEORGOPOULOS, S
KASLARIS, E
KIOUSSIS, D
KOLLIAS, G
机构
[1] AGHIA SOPHIA CHILDRENS HOSP, DEPT PATHOL, GR-11527 ATHENS, GREECE
[2] NATL INST MED RES, GENE STRUCT & EXPRESS LAB, LONDON NW7 1AA, ENGLAND
关键词
ARTHRITIS; DISEASE MODEL; GENE EXPRESSION; TNF; TRANSGENIC MICE;
D O I
10.1002/j.1460-2075.1991.tb04978.x
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
We have generated transgenic mouse lines carrying and expressing wild-type and 3'-modified human tumour necrosis factor (hTNF-alpha, cachectin) transgenes. We show that correct, endotoxin-responsive and macrophage-specific hTNF gene expression can be established in transgenic mice and we present evidence that the 3'-region of the hTNF gene may be involved in macrophage-specific transcription. Transgenic mice carrying 3'-modified hTNF transgenes shows deregulated patterns of expression and interestingly develop chronic inflammatory polyarthritis. Treatment of these arthritic mice with a monoclonal antibody against human TNF completely prevents development of this disease. Our results indicate a direct involvement of TNF in the pathogenesis of arthritis. Transgenic mice which predictably develop arthritis represent a novel genetic model by which the pathogenesis and treatment of this disease in humans may be further investigated.
引用
收藏
页码:4025 / 4031
页数:7
相关论文
共 53 条
[22]   GENES ENCODING TUMOR NECROSIS FACTOR-ALPHA AND GRANZYME-A ARE EXPRESSED DURING DEVELOPMENT OF AUTOIMMUNE DIABETES [J].
HELD, W ;
MACDONALD, HR ;
WEISSMAN, IL ;
HESS, MW ;
MUELLER, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (06) :2239-2243
[23]   EXCESSIVE PRODUCTION OF INTERLEUKIN-6/B CELL STIMULATORY FACTOR-II IN RHEUMATOID-ARTHRITIS [J].
HIRANO, T ;
MATSUDA, T ;
TURNER, M ;
MIYASAKA, N ;
BUCHAN, G ;
TANG, B ;
SATO, K ;
SHIMIZU, M ;
MAINI, R ;
FELDMAN, M ;
KISHIMOTO, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (11) :1797-1801
[24]  
HOUSSIAU FA, 1990, CLIN EXP RHEUMATOL, V8, P531
[25]   SYNOVIAL LOCALIZATION OF TUMOR NECROSIS FACTOR IN PATIENTS WITH RHEUMATOID-ARTHRITIS [J].
HUSBY, G ;
WILLIAMS, RC .
JOURNAL OF AUTOIMMUNITY, 1988, 1 (04) :363-371
[26]  
JASIN HE, 1988, METHOD ENZYMOL, V162, P379
[27]   A NOVEL ADDITION TO THE T-CELL REPERTORY - CELL-SURFACE EXPRESSION OF TUMOR-NECROSIS-FACTOR CACHECTIN BY ACTIVATED NORMAL HUMAN T-CELLS [J].
KINKHABWALA, M ;
SEHAJPAL, P ;
SKOLNIK, E ;
SMITH, D ;
SHARMA, VK ;
VLASSARA, H ;
CERAMI, A ;
SUTHANTHIRAN, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (03) :941-946
[28]   EXPRESSION AND RESCUING OF A CLONED HUMAN-TUMOR NECROSIS FACTOR GENE USING AN EBV-BASED SHUTTLE COSMID VECTOR [J].
KIOUSSIS, D ;
WILSON, F ;
DANIELS, C ;
LEVETON, C ;
TAVERNE, J ;
PLAYFAIR, JHL .
EMBO JOURNAL, 1987, 6 (02) :355-361
[29]   THE HUMAN BETA-GLOBIN GENE CONTAINS A DOWNSTREAM DEVELOPMENTAL SPECIFIC ENHANCER [J].
KOLLIAS, G ;
HURST, J ;
DEBOER, E ;
GROSVELD, F .
NUCLEIC ACIDS RESEARCH, 1987, 15 (14) :5739-5747
[30]   REGULATED EXPRESSION OF HUMAN A-GAMMA-GLOBIN, BETA-GLOBIN, AND HYBRID GAMMA-BETA-GLOBIN GENES IN TRANSGENIC MICE - MANIPULATION OF THE DEVELOPMENTAL EXPRESSION PATTERNS [J].
KOLLIAS, G ;
WRIGHTON, N ;
HURST, J ;
GROSVELD, F .
CELL, 1986, 46 (01) :89-94