Zimecki M, Webb D R, Rogers T J
Arch Immunol Ther Exp (Warsz). 1980;28(2):179-97.
Having previously established, that prostaglandins play a role in the regulation of the immune response to polyvinyl pyrollidone, a T-independent antigen, further investigations of the role of prostaglandins and cyclic nucleotides in the control of the immune response to polyvinyl pyrollidone were initiated. Strongly immunogenic (PVP 360,000) and weakly immunogenic (PVP 10,000) molecular sizes of polyvinyl pyrollidone were examined for their effects on splenic PGF2 alpha, PGE and cyclic nucleotide levels. The results show, that PVP 360,000 induces marked changes in PGF2 levels. There is an early marked depression at 2 hours after injection followed by an increase which peaks at 2 hour. At subsequent time intervals (9-10, 13-14 and 16-18 hour) high values were observed, especially in the latter case. cAMP levels undergo significant fluctuations, exhibiting very big rise at 12 and 13 hour post-immunization, cGMP levels are elevated at 2 hour declining thereafter. PGE level in C57Bl mice exhibits very substantial increase at 4-6 hour after immunization, in athymic mice, however, the increase was not significant and was preceded by a profound drop in PGE concentration. PGE level in the splenocytes from athymic mice shows a constant increase till 4 hour after PVP addition, followed by a little decrease at 6-7 hour. cAMP concentration in athymic mice exhibits a drop at 3-4 hour after immunization, followed by an increase at 5-6 hour post-immunization. Indomethacin, an inhibitor of prostaglandin synthetase, blocks the changes in PGF2 and cGMP level but has little effect on cAMP. In contrast, the weakly immunogenic form PVP 10,000 induces a large bimodal increase in cAMP levels peaking at 2 hour and again increasing between 6-8 hour; cGMP levels also rise, but more slowly. The increase in cAMP is blocked by indomethacin even though no comparable increases in PGF2 levels are observed. The changes induced by PVP 10,000 appear to be dependent on T cells since comparable changes are not observed in athymic mice. Although PVP 10,000 is non-immunogenic in normal mice or whole spleen cultures, it is immunogenic in athymic mice and purified B cell cultures. This difference has been traced to an apparent difference in the activation of T cells vs. B cells by PVP 10,000. Lastly, although inhibition of PG synthesis results in an enhancement of the immune response to PVP 360,000, no such enhancement is observed with PVP 10,000. The relevance of prostaglandin and cyclic nucleotide changes to the development of the immune response is discussed.
先前已经确定,前列腺素在对聚乙烯吡咯烷酮(一种非胸腺依赖性抗原)的免疫反应调节中发挥作用,因此启动了对前列腺素和环核苷酸在控制对聚乙烯吡咯烷酮免疫反应中的作用的进一步研究。研究了聚乙烯吡咯烷酮的强免疫原性(PVP 360,000)和弱免疫原性(PVP 10,000)分子大小对脾脏中前列腺素F2α、前列腺素E和环核苷酸水平的影响。结果显示,PVP 360,000可引起前列腺素F2水平的显著变化。注射后2小时出现早期显著下降,随后升高,并在2小时达到峰值。在随后的时间间隔(9 - 10、13 - 14和16 - 18小时)观察到较高值,尤其是在后者情况下。环磷酸腺苷(cAMP)水平经历显著波动,在免疫后12和13小时出现非常大的升高,环磷酸鸟苷(cGMP)水平在2小时升高,此后下降。C57Bl小鼠中的前列腺素E水平在免疫后4 - 6小时显著升高,然而,在无胸腺小鼠中,升高不显著,且在此之前前列腺素E浓度有大幅下降。无胸腺小鼠脾细胞中的前列腺素E水平在添加PVP后直至4小时持续升高,随后在6 - 7小时略有下降。无胸腺小鼠中的环磷酸腺苷浓度在免疫后3 - 4小时下降,随后在免疫后5 - 6小时升高。前列腺素合成酶抑制剂吲哚美辛可阻断前列腺素F2和环磷酸鸟苷水平的变化,但对环磷酸腺苷影响较小。相比之下,弱免疫原性形式的PVP 10,000可引起环磷酸腺苷水平的大幅双峰升高,在2小时达到峰值,并在6 - 8小时再次升高;环磷酸鸟苷水平也升高,但较慢。即使未观察到前列腺素F2水平有类似升高,吲哚美辛也可阻断环磷酸腺苷的升高。PVP 10,000诱导的变化似乎依赖于T细胞,因为在无胸腺小鼠中未观察到类似变化。尽管PVP 10,000在正常小鼠或全脾培养物中无免疫原性,但在无胸腺小鼠和纯化的B细胞培养物中有免疫原性。这种差异已追溯到PVP 10,000对T细胞与B细胞激活的明显差异。最后,尽管抑制前列腺素合成会增强对PVP 360,000的免疫反应,但对PVP 10,000未观察到这种增强。讨论了前列腺素和环核苷酸变化与免疫反应发展的相关性。