Kroese F G, Wubbena A S, Nieuwenhuis P
Immunology. 1986 Jan;57(1):99-104.
In this study, the relationship between germinal centre formation and the follicular trapping of immune complexes in the rat spleen was investigated. Lethally (9 Gy) X-irradiated rats were reconstituted with thoracic duct lymphocytes and subsequently challenged with sheep red blood cells to induce germinal centre formation. Rats were killed at daily intervals from 1 to 8 days after reconstitution and antigenic stimulation. Antigen trapping capacity during this interval was assessed by intravenous injection of HRP-anti-HRP immune complexes, 24 hr before killing of the animals. Germinal centre formation could be observed from Day 4 onwards. The follicular trapping capacity, which had been abolished by the X-irradiation, however, returned 2 days later (i.e. by Day 6). Apparently, in these experiments, early germinal centre formation could occur without an intact follicular trapping mechanism. It was, therefore, concluded that in this transfer system follicular immune complex trapping is not a prerequisite for the induction of de novo germinal centre formation. Previous studies have shown that both follicular dendritic cells and marginal zone B cells may play a role in the follicular antigen trapping mechanism. FDCs, as detectable with mAB MRC OX 2 in immunoperoxidase-stained frozen sections, were present in spleens at any time after irradiation and reconstitution; the impaired follicular trapping of HRP-anti-HRP immune complexes was therefore not due to an absence of FDCs. Marginal zone B cells, however, were almost absent until 5 days after reconstitution, as observed by immunohistochemical staining with anti-B cell mABs (HIS 14 and HIS 22) and a polyclonal anti-IgD antiserum. Our data suggest that regeneration of follicular antigen trapping capacity is dependent on the presence of marginal zone B cells.
在本研究中,对大鼠脾脏生发中心形成与免疫复合物的滤泡捕获之间的关系进行了调查。用9 Gy致死剂量的X射线照射大鼠,然后用胸导管淋巴细胞进行重建,随后用绵羊红细胞进行攻击以诱导生发中心形成。在重建和抗原刺激后的第1至8天,每天间隔处死大鼠。在处死动物前24小时,通过静脉注射HRP-抗HRP免疫复合物来评估此期间的抗原捕获能力。从第4天起可观察到生发中心形成。然而,X射线照射已消除的滤泡捕获能力在2天后(即第6天)恢复。显然,在这些实验中,早期生发中心形成可以在没有完整滤泡捕获机制的情况下发生。因此,得出的结论是,在这个转移系统中,滤泡免疫复合物捕获不是诱导新生发中心形成的先决条件。先前的研究表明,滤泡树突状细胞和边缘区B细胞可能在滤泡抗原捕获机制中发挥作用。在免疫过氧化物酶染色的冰冻切片中用单克隆抗体MRC OX 2可检测到的滤泡树突状细胞,在照射和重建后的任何时间都存在于脾脏中;因此,HRP-抗HRP免疫复合物的滤泡捕获受损并非由于滤泡树突状细胞的缺失。然而,通过用抗B细胞单克隆抗体(HIS 14和HIS 22)和多克隆抗IgD抗血清进行免疫组织化学染色观察到,边缘区B细胞在重建后5天之前几乎不存在。我们的数据表明,滤泡抗原捕获能力的再生依赖于边缘区B细胞的存在。