Samulowitz Ulrike, Weber Markus, Weeratna Risini, Uhlmann Eugen, Noll Bernhard, Krieg Arthur M, Vollmer Jörg
Coley Pharmaceutical GmbH--A Pfizer Company, Düsseldorf, Germany.
Oligonucleotides. 2010 Apr;20(2):93-101. doi: 10.1089/oli.2009.0210.
Unmethylated deoxycytidyl-deoxyguanosin dinucleotide (CpG)-containing oligodeoxynucleotides (ODNs) have been well characterized as agonists for Toll-like receptor 9. We here describe a new class of CpG ODNs, the so-called P-Class, which combines preferred properties of known CpG ODN classes. This P-Class contains two palindromic sequences, enabling it to form concatamers, multimeric units, where each molecule is bound via Watson-Crick basepairing to a second and a third palindrome. The type I interferon-inducing potency and efficacy of the double-palindromic P-Class ODN is substantially higher than that of previously described C-Class ODNs, and they stimulate superior cytokine production upon in vivo application. The multimeric structures of the P-Class can be resolved to monomers and dimers by formulation in low-salt buffer, retaining the strong and potent immune effects. Taken together, we have discovered a novel class of CpG ODNs, the P-Class, with promising superior activity for disease application.
含未甲基化脱氧胞苷 - 脱氧鸟苷二核苷酸(CpG)的寡脱氧核苷酸(ODN)已被充分表征为Toll样受体9的激动剂。我们在此描述了一类新的CpG ODN,即所谓的P类,它结合了已知CpG ODN类别的优选特性。该P类包含两个回文序列,使其能够形成串联体,即多聚体单元,其中每个分子通过沃森 - 克里克碱基配对与第二个和第三个回文序列结合。双回文P类ODN诱导I型干扰素的效力和功效显著高于先前描述的C类ODN,并且它们在体内应用时刺激产生更优的细胞因子。通过在低盐缓冲液中配制,P类的多聚体结构可以分解为单体和二聚体,同时保留强大的免疫效应。综上所述,我们发现了一类新型的CpG ODN,即P类,在疾病应用方面具有有望的卓越活性。