一类新的免疫刺激CpG寡脱氧核苷酸在I型干扰素诱导中具有较高的效力和优先的结构特性。

Ulrike Samulowitz, Markus Weber, Risini Weeratna, Eugen Uhlmann, Bernhard Noll, Arthur M Krieg, Jörg Vollmer
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引用次数: 73

摘要

未甲基化脱氧胞苷-脱氧鸟苷二核苷酸(CpG)-含寡脱氧核苷酸(odn)已被很好地表征为toll样受体9的激动剂。我们在这里描述了一类新的CpG ODN,即所谓的p类,它结合了已知CpG ODN类的首选特性。这个p类包含两个回文序列,使其能够形成串联体,多聚体单元,其中每个分子通过沃森-克里克碱基修复与第二个和第三个回文结合。双回文p类ODN诱导I型干扰素的效力和疗效大大高于先前描述的c类ODN,并且在体内应用后,它们可以刺激更好的细胞因子产生。通过在低盐缓冲液中配制,P-Class的多聚体结构可分解为单体和二聚体,保留了强而有力的免疫效果。综上所述,我们发现了一类新的CpG ODNs, P-Class,具有良好的疾病应用活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel class of immune-stimulatory CpG oligodeoxynucleotides unifies high potency in type I interferon induction with preferred structural properties.

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.

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来源期刊
Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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