Structure, mechanism and therapeutic utility of immunosuppressive oligonucleotides.

Structure, mechanism and therapeutic utility of immunosuppressive oligonucleotides.
复制标题

DOI:
10.1016/j.phrs.2015.11.010
复制
发表时间:
2016-03
影响因子:
9.3
通讯作者:
Klinman DM
Klinman DM
中科院分区:
医学1区
文献类型:
--
作者:
Bayik D;Gursel I;Klinman DM

文献摘要

参考文献

被引文献

相似文献

可以下调免疫系统细胞成分的合成寡脱氧核苷酸已经被开发出来,并正在临床前模型中进行广泛研究。这些药物的序列、作用机制和细胞靶标各不相同,但都具有抑制过多炎症反应的能力。这项工作回顾了免疫抑制性寡脱氧核苷酸 (Sup ODN) 的类型,并比较了它们对以免疫刺激病理水平为特征的疾病的治疗活性,范围从自身免疫到感染性休克到癌症(参见图解摘要)。考虑了 Sup ODN 功效的潜在机制以及大小、序列和核苷酸骨架对功能的影响。
Synthetic oligodeoxynucleotides that can down-regulate cellular elements of the immune system have been developed and are being widely studied in preclinical models. These agents vary in sequence, mechanism of action, and cellular target(s) but share the ability to suppress a plethora of inflammatory responses. This work reviews the types of immunosuppressive oligodeoxynucleotide (Sup ODN) and compares their therapeutic activity against diseases characterized by pathologic levels of immune stimulation ranging from autoimmunity to septic shock to cancer (see graphical abstract). The mechanism(s) underlying the efficacy of Sup ODN and the influence size, sequence and nucleotide backbone on function are considered.
DOI: 10.4049/jimmunol.171.3.1393
发表时间: 2003-08-01
影响因子: 4.4
作者:
Gursel, I;Gursel, M;Klinman, DM
通讯作者: Klinman, DM
一种寡脱氧核苷酸,能够减轻流感病毒感染小鼠的急性肺部炎症损伤。
DOI: 10.1016/j.bbrc.2011.10.062
发表时间: 2011-11-18
影响因子: 3.1
作者:
Fang, Mingli;Wan, Min;Hua, Shucheng
通讯作者: Hua, Shucheng
DOI: 10.1155/2013/217297
发表时间: 2013
影响因子: 4.6
作者:
Boehm O;Markowski P;van der Giet M;Gielen V;Kokalova A;Brill C;Hoeft A;Baumgarten G;Meyer R;Knuefermann P
通讯作者: Knuefermann P
DOI: 10.1038/nprot.2009.120
发表时间: 2009
期刊: Nature protocols
影响因子: 14.8
作者:
通讯作者: --
DOI: 10.1084/jem.20101048
发表时间: 2010-12-20
期刊: The Journal of experimental medicine
影响因子: --
作者:
Guiducci C;Tripodo C;Gong M;Sangaletti S;Colombo MP;Coffman RL;Barrat FJ
通讯作者: Barrat FJ