IN-VITRO INHIBITION OF MURINE IFN-GAMMA PRODUCTION BY PHOSPHOROTHIOATE DEOXYGUANOSINE OLIGOMERS

被引:51
作者
HALPERN, MD [1 ]
PISETSKY, DS [1 ]
机构
[1] DUKE UNIV, MED CTR, DIV RHEUMATOL & IMMUNOL, DURHAM, NC 27705 USA
来源
IMMUNOPHARMACOLOGY | 1995年 / 29卷 / 01期
关键词
ANTISENSE THERAPY; IFN-GAMMA; PHOSPHOROTHIOATE OLIGONUCLEOTIDE; CYTOKINE;
D O I
10.1016/0162-3109(95)00043-S
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Phosphorothioate (PT) oligonucleotides are designed as specific agents for antisense therapy although they have been reported to exert non-specific immunomodulatory effects. To elucidate further their actions, the effect of PT deoxyguanosine oligomers (S-oligo(dG)) on in vitro cytokine production by mouse splenocytes was studied. S-oligo(dG)(20) inhibited production of INF gamma induced by Con A, E. coli DNA or the combination of PMA and calcium ionophore A23187. The diester analogue was inactive, and of PT homo-oligomers tested, S-oligo(dG)(20) was the most active. PT compounds with as few as 5 dG residues could also block INF gamma production. These results indicate that base composition and length, as well as the PT backbone, contribute to the inhibition of INF gamma production and extend the range of immunomodulatory effects of PT compounds.
引用
收藏
页码:47 / 52
页数:6
相关论文
共 26 条
[1]  
Akhtar S, 1992, Trends Cell Biol, V2, P139, DOI 10.1016/0962-8924(92)90100-2
[2]  
BANCROFT GJ, 1989, J IMMUNOL, V143, P127
[3]   IMMUNE STIMULATION BY AN ANTISENSE OLIGOMER COMPLEMENTARY TO THE REV GENE OF HIV-1 [J].
BRANDA, RF ;
MOORE, AL ;
MATHEWS, L ;
MCCORMACK, JJ ;
ZON, G .
BIOCHEMICAL PHARMACOLOGY, 1993, 45 (10) :2037-2043
[4]  
CHIANG MY, 1991, J BIOL CHEM, V266, P18162
[5]  
CHUNG IK, 1991, J BIOL CHEM, V266, P9508
[6]   PROPERTIES OF BGP1, A POLY(DG)-BINDING PROTEIN FROM CHICKEN ERYTHROCYTES [J].
CLARK, SP ;
LEWIS, CD ;
FELSENFELD, G .
NUCLEIC ACIDS RESEARCH, 1990, 18 (17) :5119-5126
[7]   OLIGONUCLEOTIDES AS THERAPEUTIC AGENTS [J].
COHEN, JS .
PHARMACOLOGY & THERAPEUTICS, 1991, 52 (02) :211-225
[8]  
CROOKE RM, 1991, ANTI-CANCER DRUG DES, V6, P609
[9]  
CROOKE ST, 1992, ANNU REV PHARMACOL, V32, P329
[10]   INCREASED SPECIFICITY FOR ANTISENSE OLIGODEOXYNUCLEOTIDE TARGETING OF RNA CLEAVAGE BY RNASE-H USING CHIMERIC METHYLPHOSPHONODIESTER PHOSPHODIESTER STRUCTURES [J].
GILES, RV ;
TIDD, DM .
NUCLEIC ACIDS RESEARCH, 1992, 20 (04) :763-770