SOLUBLE INTERLEUKIN-6 RECEPTOR IS BIOLOGICALLY-ACTIVE IN-VIVO

被引:48
作者
MACKIEWICZ, A
WIZNEROWICZ, M
ROEB, E
KARCZEWSKA, A
NOWAK, J
HEINRICH, PC
ROSEJOHN, S
机构
[1] GREAT POLANT CANC CTR,ACAD MED,CHAIR ONCOL,DEPT CANC IMMUNOL,PL-61688 POZNAN,POLAND
[2] POLISH ACAD SCI,INST HUMAN GENET,PL-60476 POZNAN,POLAND
[3] RHEIN WESTFAL TH AACHEN,INST BIOCHEM,D-52057 AACHEN,GERMANY
关键词
GENE THERAPY; INTERLEUKIN; 6; LEUKEMIA INHIBITORY FACTOR; MELANOMA; SOLUBLE INTERLEUKIN 6-RECEPTOR;
D O I
10.1006/cyto.1995.1019
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
A cancer cell transfection model was used to evaluate biological activity of soluble IL-6 receptor (sIL-6R) in vivo, B-78 melanoma cells were stably transfected with cDNAs encoding human IL-6, murine sIL-6R and human leukaemia inhibitory factor (LIF). Control and transfected cells were intravenously (i.v.) and/or subcutaneously (s.c.) injected into B57BL/6 x C3H or SCID mice. Whereas B-78 cells formed tumours and lung metastasis in injected animals, transfected animals, transfected cells showed greatly reduced tumour and metastasis formation. Transfection of IL-6, sIL-6R or LIF had similar protective effects. The combination of IL-6 and sIL-6R was most effective. Kinetic analysis demonstrated a 3 week lag period between formation of tumours by B-78 cells and the combination of B-78 cells transfected with IL-6 and sIL-6R, No such lag phase was seen when B-78-IL-6 or B-78-IL-6 or B-78-sIL-6R were injected alone, These results indicate that IL-6 alone exhibits a different quality of activity when compared to the IL-6-soluble receptor complex, Our results demonstrate for the first time that sIL-6R is a biologically active molecule in vivo.
引用
收藏
页码:142 / 149
页数:8
相关论文
共 58 条
[1]   PRODUCTION OF HYBRIDOMA GROWTH-FACTOR BY HUMAN-MONOCYTES [J].
AARDEN, LA ;
DEGROOT, ER ;
SCHAAP, OL ;
LANSDORP, PM .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (10) :1411-1416
[2]  
ASHER AL, 1991, J IMMUNOL, V146, P3227
[3]   MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250
[4]   CYTOKINE GENE-TRANSFER IN TUMOR-INHIBITION AND TUMOR-THERAPY - WHERE ARE WE NOW [J].
COLOMBO, MP ;
FORNI, G .
IMMUNOLOGY TODAY, 1994, 15 (02) :48-51
[5]   LIFR-BETA AND GP-130 AS HETERODIMERIZING SIGNAL TRANSDUCERS OF THE TRIPARTITE CNTF RECEPTOR [J].
DAVIS, S ;
ALDRICH, TH ;
STAHL, N ;
PAN, L ;
TAGA, T ;
KISHIMOTO, T ;
IP, NY ;
YANCOPOULOS, GD .
SCIENCE, 1993, 260 (5115) :1805-1808
[6]   IMMUNOLOGICAL AND NONIMMUNOLOGICAL INFLUENCE OF H-2KB GENE TRANSFECTION ON THE METASTATIC ABILITY OF B16 MELANOMA-CELLS [J].
DEGIOVANNI, C ;
PALMIERI, G ;
NICOLETTI, G ;
LANDUZZI, L ;
SCOTLANDI, K ;
BONTADINI, A ;
TAZZARI, PL ;
SENSI, M ;
SANTONI, A ;
NANNI, P ;
LOLLINI, PL .
INTERNATIONAL JOURNAL OF CANCER, 1991, 48 (02) :270-276
[7]   THE MATRIX METALLOPROTEINASES AND THEIR NATURAL INHIBITORS - PROSPECTS FOR TREATING DEGENERATIVE TISSUE-DISEASES [J].
DOCHERTY, AJP ;
OCONNELL, J ;
CRABBE, T ;
ANGAL, S ;
MURPHY, G .
TRENDS IN BIOTECHNOLOGY, 1992, 10 (06) :200-207
[8]   VACCINATION WITH IRRADIATED TUMOR-CELLS ENGINEERED TO SECRETE MURINE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR STIMULATES POTENT, SPECIFIC, AND LONG-LASTING ANTITUMOR IMMUNITY [J].
DRANOFF, G ;
JAFFEE, E ;
LAZENBY, A ;
GOLUMBEK, P ;
LEVITSKY, H ;
BROSE, K ;
JACKSON, V ;
HAMADA, H ;
PARDOLL, D ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3539-3543
[9]   A GROWTH-RESPONSIVE GENE (16C8) IN NORMAL MOUSE FIBROBLASTS HOMOLOGOUS TO A HUMAN COLLAGENASE INHIBITOR WITH ERYTHROID-POTENTIATING ACTIVITY - EVIDENCE FOR INDUCIBLE AND CONSTITUTIVE TRANSCRIPTS [J].
EDWARDS, DR ;
WATERHOUSE, P ;
HOLMAN, ML ;
DENHARDT, DT .
NUCLEIC ACIDS RESEARCH, 1986, 14 (22) :8863-8878
[10]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13