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Toll 样受体 7/8 激动剂在疫苗佐剂中的应用。

The use of Toll-like receptor 7/8 agonists as vaccine adjuvants.

机构信息

Drug Delivery Systems Division, 3M Center, Building 260-4S-13, St Paul, MN 55144, USA.

出版信息

Expert Rev Vaccines. 2013 Jul;12(7):809-19. doi: 10.1586/14760584.2013.811208.

Abstract

Small molecule Toll-like receptor (TLR) 7/8 agonists have demonstrated potential as vaccine adjuvants, since they directly activate APCs and can enhance both humoral and cellular immune responses, especially Th1 responses. Although the natural ligands for TLR7 and TLR8 are ssRNA, the vast majority of vaccine studies performed thus far have been performed with synthetic small molecule imidazoquinolines, such as imiquimod and resiquimod. Despite the approved clinical use of the topical TLR7 agonist, imiquimod (Aldara(®) Imiquimod 5% cream; 3M, MN, USA), for external genital warts, superficial basal cell carcinoma and actinic keratosis, no vaccines using TLR7, TLR8 or TLR7/8 agonists have progressed beyond early-phase clinical studies thus far. This review will highlight the nonclinical and clinical studies that indicate promise for TLR7/8 ligands as vaccine adjuvants, reasons for inconsistent results thus far, problems with current technology and potential paths forward for TLR7/8 agonists as vaccine adjuvants.

摘要

小分子 Toll 样受体 (TLR) 7/8 激动剂已被证明具有作为疫苗佐剂的潜力,因为它们直接激活 APCs,并能增强体液和细胞免疫应答,特别是 Th1 应答。尽管 TLR7 和 TLR8 的天然配体是 ssRNA,但迄今为止进行的绝大多数疫苗研究都是用合成的小分子咪唑并喹啉进行的,如咪喹莫特和瑞喹莫特。尽管局部 TLR7 激动剂,咪喹莫特(Aldara(®) Imiquimod 5% cream;3M,MN,USA)已被批准用于治疗外生殖器疣、浅表基底细胞癌和光化性角化病,但迄今为止,尚无使用 TLR7、TLR8 或 TLR7/8 激动剂的疫苗进入早期临床研究阶段。本综述将重点介绍非临床和临床研究,这些研究表明 TLR7/8 配体作为疫苗佐剂具有潜力,以及迄今为止结果不一致的原因、当前技术存在的问题以及 TLR7/8 激动剂作为疫苗佐剂的潜在途径。

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