Macatonia S E, Knight S C, Edwards A J, Griffiths S, Fryer P
Division of Rheumatology, Clinical Research Centre, Harrow, United Kingdom.
J Exp Med. 1987 Dec 1;166(6):1654-67. doi: 10.1084/jem.166.6.1654.
We have examined the cells involved in the development of contact sensitivity to FITC in CBA mice. After skin painting with antigen, the number of dendritic cells (DC) in the draining lymph nodes increased by 30 min, was maximal at 48 h, and returned to normal by 6 d. Derivation of some DC from Langerhans' cells of the skin was indicated from the presence of Birbeck granules observed in some DC isolated 24 h after skin painting. The DC acquired FITC and by 8 h there were two populations, one highly fluorescent and the other less fluorescent. The highly fluorescent cells were present between 8 h and 3 d after sensitization, and during this period the DC were potent at initiating primary proliferative responses of normal syngeneic T lymphocytes in vitro. Between days 3 and 5 the numbers of lymphocytes in the draining lymph node increased. During this period purified T lymphocytes did not express detectable levels of antigen, but enriched B cell populations expressed antigen transiently on day 1, 2, or 3 after exposure to antigen. The results showed that, during a 3-d period after exposure to antigen, DC expressed antigen and stimulated T cell proliferation. We speculate that low amounts of FITC binding selectively to veiled cells or lymph node DC in the first hours after exposure to antigen are not immunogenic but that Langerhans' cells acquire high levels of antigen, enter the nodes, and initiate immune responses.
我们已经研究了CBA小鼠中对异硫氰酸荧光素(FITC)产生接触敏感性过程中涉及的细胞。在用抗原进行皮肤涂抹后,引流淋巴结中的树突状细胞(DC)数量在30分钟时增加,在48小时时达到最大值,并在6天时恢复正常。从皮肤涂抹24小时后分离出的一些DC中观察到伯贝克颗粒,表明部分DC来源于皮肤的朗格汉斯细胞。DC摄取了FITC,到8小时时出现两个群体,一个高荧光,另一个低荧光。高荧光细胞在致敏后8小时至3天存在,在此期间,DC在体外能够有效启动正常同基因T淋巴细胞的原发性增殖反应。在第3天至第5天期间,引流淋巴结中的淋巴细胞数量增加。在此期间,纯化的T淋巴细胞未表达可检测水平的抗原,但富集的B细胞群体在接触抗原后的第1、2或3天短暂表达抗原。结果表明,在接触抗原后的3天内,DC表达抗原并刺激T细胞增殖。我们推测,在接触抗原后的最初几个小时内,少量选择性结合到隐蔽细胞或淋巴结DC上的FITC没有免疫原性,但朗格汉斯细胞摄取高水平抗原,进入淋巴结并启动免疫反应。