Institute of Immunology and Infection Research, University of Edinburgh, Edinburgh, EH9 3JT, United Kingdom.
Curr Opin Immunol. 2011 Feb;23(1):119-23. doi: 10.1016/j.coi.2010.09.006. Epub 2010 Oct 13.
Understanding the initiation of cellular immune responses during blood-stage malaria infection is essential for the development of an effective vaccine that improves upon the naturally acquired immune response and induces rapid and long-lasting protection against disease. Recent studies have identified the dendritic cell (DC) subtypes responsible for priming Plasmodium-specific T cells that mediate protection and/or pathology during blood-stage infection. Significant progress has also been made towards understanding DC recognition of Plasmodium parasites through engagement of TLR signalling pathways, as well as the potential for non-TLR ligands to mediate Plasmodium-induced suppression of DC antigen presentation.
了解在疟原虫血期感染期间细胞免疫应答的启动对于开发有效的疫苗至关重要,这种疫苗可以改善自然获得的免疫应答,并诱导对疾病的快速和持久保护。最近的研究已经确定了树突状细胞 (DC) 亚型,这些亚型负责启动对保护和/或疟原虫血症感染期间发病机制有介导作用的疟原虫特异性 T 细胞。在理解 DC 通过 TLR 信号通路识别疟原虫寄生虫方面,以及非 TLR 配体在介导疟原虫诱导的 DC 抗原呈递抑制方面,也取得了重大进展。