Krco C J, Johnson E, David C S, Tomasi T B
J Immunogenet. 1979 Dec;6(6):439-46. doi: 10.1111/j.1744-313x.1979.tb00698.x.
The ability of mouse amniotic fluid (MAF), alpha-foetoprotein (AFP) and MAF depleted of AFP (MAF - AFP) to suppress primary one-way MLR's was investigated. It was found that MAF, AFP and MAF - AFP were all suppressive of MLR's specific for MHC, K, D or I + S determinants. Suppression was observed when either lymph node or spleen cells were used as the responder cells. Nylon wool column passage of these cells did not significantly affect the immunosuppressive action of these substances. In contrast, MLR's specific for non-MHC/M-locus determinants demonstrated either diminished suppression or augmentation of the response, compared with the MHC stimulated MLR's. Our results show a differential effect of whole MAF and its fractions on the proliferative responses induced by various allogeneic stimuli and suggest that suppression is not due to a non-specific effect on proliferation regardless of the stimulus or cell type involved.
研究了小鼠羊水(MAF)、甲胎蛋白(AFP)以及去除AFP的MAF(MAF - AFP)抑制单向初次混合淋巴细胞反应(MLR)的能力。结果发现,MAF、AFP和MAF - AFP均能抑制针对主要组织相容性复合体(MHC)、K、D或I + S决定簇的MLR。当使用淋巴结或脾细胞作为反应细胞时,均可观察到抑制作用。这些细胞经尼龙毛柱传代后,这些物质的免疫抑制作用未受到显著影响。相比之下,与MHC刺激的MLR相比,针对非MHC/M基因座决定簇的MLR表现出抑制作用减弱或反应增强。我们的结果显示,完整的MAF及其组分对各种同种异体刺激诱导的增殖反应具有不同的影响,并表明抑制作用并非由于对增殖的非特异性影响,而与所涉及的刺激或细胞类型无关。