Müller-Quernheim J, Botzenhardt U, von Steldern D, Lefkovits I
Institut für Medizinische Mikrobiologie, Johannes Gutenberg-Universität, Mainz, FRG.
Int Arch Allergy Appl Immunol. 1988;85(2):219-26. doi: 10.1159/000234506.
The T cells of NZB mice become hyperreactive after stimulation with minor histocompatibility (MIH) antigens. This hyperreactivity has previously been demonstrated only for cytotoxic T cells of NZB, although there was some evidence for an increase of their T-helper cell activity facilitating the response. Here we report a quantitative analysis of T-cell help and help of T-cell subpopulations against autologous, MIH, and H-2 antigens in a limiting dilution assay. After stimulation of NZB T cells with autologous and H-2 antigens, the T-helper cell frequencies did not differ from that of normal mice. After stimulation with MIH antigens however, Lyt 1+2+ T-cells of NZB showed a higher response than those of BALB/c origin. The same difference was seen after prestimulation with ConA or the specific antigen. This demonstrates that NZB-helper cells are more easily activated by weak antigenic differences, and it is possible that this contributes to the prevalence of autoimmune disease in this strain.
用次要组织相容性(MIH)抗原刺激后,NZB小鼠的T细胞会变得反应过度。此前这种反应过度仅在NZB的细胞毒性T细胞中得到证实,不过有一些证据表明其辅助性T细胞活性增加有助于这种反应。在此我们报告了在有限稀释分析中针对自体、MIH和H-2抗原的T细胞辅助以及T细胞亚群辅助的定量分析。用自体和H-2抗原刺激NZB T细胞后,辅助性T细胞频率与正常小鼠无异。然而,用MIH抗原刺激后,NZB的Lyt 1+2+ T细胞比BALB/c来源的细胞表现出更高的反应。用刀豆蛋白A(ConA)或特异性抗原预刺激后也出现了同样的差异。这表明NZB辅助性T细胞更容易被微弱的抗原差异激活,并且这可能是该品系自身免疫性疾病高发的原因之一。