Knight S C, Askonas B A, Macatonia S E
Antigen Presentation Research Group, Imperial College School of Medicine at Northwick Park Institute for Medical Research, Middlesex, United Kingdom.
Adv Exp Med Biol. 1997;417:389-94. doi: 10.1007/978-1-4757-9966-8_63.
Dendritic cells (DC) carry antigen into lymph nodes where they may cluster with CD4 and CD8+ lymphocytes and activate both subsets in the initiation of immune responses. Since DC do not leave the lymph nodes in the efferent lymph they may die within the lymph nodes. Another possibility is that they are targets for cytotoxic T cells (CTL) when expressing appropriate epitopes. This possibility was tested in vitro using human peripheral blood DC to stimulate the development of primary CTL in response to HIV-1 or one of its T-cell epitopes (e.g. env 111-126) and secondary CTL in response to type A influenza virus. Pooled CTL generated during six day cultures in 60 replicate 20 microliters hanging drops were tested in a conventional CTL assay. The HIV or HIV peptide stimulated CTL lysed HIV infected DC while the influenza-virus induced CTL killed DC targets infected with this virus. DC were not lysed significantly until they had been exposed to virus for 2-3 days and thus are not highly susceptible to lysis. However, killing of DC after 2-3 days infection with virus may be a feedback mechanism for removing antigen presenting cells after they have stimulated T cell responses. Removal of persistently infected DC by CD8+ CTL may also contribute to the reduction in DC numbers observed in blood and skin in HIV infection.
树突状细胞(DC)将抗原带入淋巴结,在那里它们可能与CD4和CD8 +淋巴细胞聚集,并在免疫反应启动时激活这两个亚群。由于DC不会随输出淋巴离开淋巴结,它们可能在淋巴结内死亡。另一种可能性是,当它们表达适当的表位时,它们是细胞毒性T细胞(CTL)的靶标。使用人外周血DC在体外测试了这种可能性,以刺激针对HIV-1或其T细胞表位之一(例如env 111-126)的原发性CTL的发育以及针对甲型流感病毒的继发性CTL的发育。在60个重复的20微升悬滴中进行六天培养期间产生的汇集CTL在常规CTL测定中进行测试。HIV或HIV肽刺激的CTL裂解被HIV感染的DC,而流感病毒诱导的CTL杀死被该病毒感染的DC靶标。直到DC暴露于病毒2 - 3天后才会被显著裂解,因此它们对裂解不是高度敏感。然而,病毒感染2 - 3天后DC的杀伤可能是一种反馈机制,用于在抗原呈递细胞刺激T细胞反应后将其清除。CD8 + CTL清除持续感染的DC也可能导致在HIV感染的血液和皮肤中观察到的DC数量减少。