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体外脾细胞真正的初次免疫反应中涉及的细胞事件。

Cellular events involved in the true primary immune response of splenocytes in vitro.

作者信息

Friedman H, Kamo I, Kateley J

出版信息

Adv Exp Med Biol. 1976;66:107-15. doi: 10.1007/978-1-4613-4355-4_16.

Abstract

An antibody response showing characteristics of a "true" primary response was readily induced in vitro with splenocytes from normal non-immunized animals cultured with strongly immunogenic Vibrio cholerae somatic antigens. Prior studies have shown that the response to vibrios in intact animals appeared to be a true primary response since no pre-existing antibody forming cells were present in non-immunized animals and the antigen induced response, following a lag of two days, resulted thereafter in a rapid stepwise increase in the number of specific PFCs, reaching a peak at 12 to 14 days. Using the Marbrook culture system for antibody formation a readily detected immunocyte response to vibrios was induced with splenocytes from normal non-immunized animals. No background antibody forming cells developed to the organisms without addition of vibrios in vitro. After in vitro immunization with 10(6) bacteria significant numbers of IgM PFCs appeared with a peak response on days 7 to 8. Splenocyte cultures from mice primed earlier with vibrios developed a marked secondary response, with appearance of both IgM and IgG PFCs. Large numbers of both classes of PFCs developed, with peak responses on days 6 to 7, similar to the "primary" response to sheep erythrocytes. However, significant numbers of PFCs to vibrios developed in cultures of vibrio-primed cultures even in the absence of vibrios during the 12 day culture period. The availability of a completely in vitro model system to induce a true primary immune response without the complication of pre-existing background antibody forming cells will be of value for further studies concerning various cellular pathways and interactions during the immune response to small amounts of strongly immunogenic bacterial antigens.

摘要

用来自正常未免疫动物的脾细胞与强免疫原性霍乱弧菌体抗原在体外培养,可轻易诱导出呈现“真正”初次应答特征的抗体应答。先前的研究表明,完整动物对弧菌的应答似乎是真正的初次应答,因为未免疫动物中不存在预先存在的抗体形成细胞,且抗原诱导的应答在滞后两天后,导致特异性PFC数量迅速逐步增加,在12至14天达到峰值。使用马尔布鲁克抗体形成培养系统,可诱导来自正常未免疫动物的脾细胞对弧菌产生易于检测到的免疫细胞应答。在体外不添加弧菌的情况下,未产生针对这些生物体的背景抗体形成细胞。用10(6)个细菌进行体外免疫后,大量IgM PFC出现,在第7至8天出现峰值应答。早期用弧菌致敏的小鼠的脾细胞培养物产生明显的二次应答,同时出现IgM和IgG PFC。两类PFC都大量产生,在第6至7天出现峰值应答,类似于对绵羊红细胞的“初次”应答。然而,即使在12天培养期内没有弧菌,在弧菌致敏培养物的培养物中也产生了大量针对弧菌的PFC。一个完全体外模型系统的可用性,可在没有预先存在的背景抗体形成细胞的复杂情况下诱导真正的初次免疫应答,对于进一步研究针对少量强免疫原性细菌抗原的免疫应答过程中的各种细胞途径和相互作用将具有价值。

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