The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3052, Australia.
Trends Immunol. 2012 Feb;33(2):71-7. doi: 10.1016/j.it.2011.10.007. Epub 2011 Dec 6.
Delivering antigens directly to dendritic cells (DCs) in situ, by injecting antigens coupled to antibodies specific for DC surface molecules, is a promising strategy for enhancing vaccine efficacy. Enhanced cytotoxic T cell responses are obtained if an adjuvant is co-administered to activate the DC. Such DC targeting is also effective at enhancing humoral immunity, via the generation of T follicular helper cells. Depending on the DC surface molecule targeted, antibody production can be enhanced even in the absence of adjuvants. In the case of Clec9A as the DC surface target, enhanced antibody production is a consequence of the DC-restricted expression of the target molecule. Few other cells absorb the antigen-antibody construct, therefore, it persists in the bloodstream, allowing sustained antigen presentation, even by non-activated DCs.
将与树突状细胞 (DC) 表面分子特异性抗体偶联的抗原直接递送至 DC 原位,是增强疫苗效力的一种有前途的策略。如果同时给予佐剂以激活 DC,则可以获得增强的细胞毒性 T 细胞反应。通过生成滤泡辅助 T 细胞,这种 DC 靶向也可以有效地增强体液免疫。根据靶向的 DC 表面分子,即使没有佐剂,抗体的产生也可以增强。在 Clec9A 作为 DC 表面靶标的情况下,抗体产生的增强是由于靶分子在 DC 上的受限表达所致。很少有其他细胞吸收抗原-抗体复合物,因此,它在血液中持续存在,允许即使是非激活的 DC 也能持续进行抗原呈递。