CpG motif identification for veterinary and laboratory species demonstrates that sequence recognition is highly conserved

被引:191
作者
Rankin, R
Pontarollo, R
Ioannou, X
Krieg, AM
Hecker, R
Babiuk, LA
van Drunen, S
van den Hurk, LV
机构
[1] Univ Saskatchewan, Vet Infect Dis Org, Saskatoon, SK 57N 5E3, Canada
[2] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[3] Vet Affairs Med Ctr, Iowa City, IA 52242 USA
[4] Coley Pharmaceut Grp, Wellesley, MA 02481 USA
[5] Qiagen GMBH, Hilden, Germany
来源
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT | 2001年 / 11卷 / 05期
关键词
D O I
10.1089/108729001753231713
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
Oligodinucleotides containing CpG motifs stimulate vertebrate immune cells in vitro, have proven efficacy in murine disease models and are currently being tested in human clinical trials as therapies for cancer, allergy, and infectious disease. As there are no known immunostimulatory motifs for veterinary species, the potential of CpG DNA as a veterinary pharmaceutical has not been investigated. Here, optimal CpG motifs for seven veterinary and three laboratory species are described. The preferential recognition of a GTCGTT motif was strongly conserved across two vertebrate phyla, although a GACGTT motif was optimal for inbred strains of mice and rabbits. In a subsequent adjuvanticity trial, the in vitro screening methodology was validated in sheep, representing the first demonstration of CpG DNA efficacy in a veterinary species. These results should provide candidate immunostimulant and therapeutic drugs for veterinary use and enable the testing of CpG DNA in large animal models of human disease.
引用
收藏
页码:333 / 340
页数:8
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