Panter Gabriela, Kuznik Alenka, Jerala Roman
Faculty of Chemistry and Chemical Technology, University of Ljubljana, Hajdrihova 19, Ljubljana, Slovenia.
Curr Opin Mol Ther. 2009 Apr;11(2):133-45.
Intracellular TLRs, represented by TLRs 3, 7, 8 and 9, are specialized for the recognition of different types of microbe-derived nucleic acids. However, endogenous nucleic acids can also activate these TLRs, triggering autoimmunity. Nucleic acid-sensing TLRs initiate innate immune responses upon infection, but these receptors also initiate the development of protective adaptive immune responses. Therefore, TLR stimulation represents an attractive strategy for the development of therapeutic and prophylactic agents targeting microbial infections, cancers and allergies. The current use of stimulatory nucleic acids targeting TLRs is reviewed for applications ranging from vaccine adjuvants to anticancer, antiviral and anti-allergic agents. In addition, inhibitory nucleic acid ligands being evaluated for their ability to ameliorate autoimmune disorders and viremias, such as systemic lupus erythematosus and HIV infection, respectively, are described.
以Toll样受体3、7、8和9为代表的细胞内Toll样受体专门用于识别不同类型的微生物衍生核酸。然而,内源性核酸也可激活这些Toll样受体,引发自身免疫。核酸传感Toll样受体在感染时启动固有免疫反应,但这些受体也启动保护性适应性免疫反应的发展。因此,Toll样受体刺激代表了一种有吸引力的策略,可用于开发针对微生物感染、癌症和过敏的治疗和预防药物。本文综述了目前靶向Toll样受体的刺激性核酸在从疫苗佐剂到抗癌、抗病毒和抗过敏药物等各种应用中的使用情况。此外,还描述了正在评估的抑制性核酸配体,它们分别具有改善自身免疫性疾病和病毒血症(如系统性红斑狼疮和HIV感染)的能力。