Karanikas V, Rowley M J, MacKay I R, Loveland B E
Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia.
Immunology. 1999 Jun;97(2):264-71. doi: 10.1046/j.1365-2567.1999.00762.x.
Standard methods to generate autoimmune reactions in mice, by immunization with antigens emulsified with adjuvants, stimulate strong helper (CD4) T-cell and antibody responses but are not reported to induce cytolytic CD8 T cells. The aim of this study was to assess whether specific autoreactive CD8 T cells could be readily generated after immunization with a 'weak' autoantigen in adjuvant. Mice were immunized intraperitoneally three times with the E3 subunit of the mitochondrial 2-oxoacid dehydrogenase enzyme complexes (dihydrolipoamide dehydrogenase) emulsified with Freund's complete adjuvant. Splenic and lymph node lymphocytes were harvested after 14 days for in vitro functional studies. T lymphocytes were tested for proliferative responses and cytotoxicity against antigen-loaded isogeneic target cells. An autoreactive cytolytic T lymphocyte (CTL) response was detectable only after the in vitro restimulation of lymphocytes with E3 antigen-loaded syngeneic splenocytes. These CTL were identified as H-2-restricted CD8+ T cells. A proliferative response to E3 was demonstrable against antigen-pulsed syngeneic splenocytes. Immunized mice also generated strong antibody responses to E3. Liver histology showed portal infiltrates interpreted as a response of the liver to a non-specific immunological stimulus. It is concluded that autoreactive cytolytic T cells can be generated experimentally upon appropriate stimulation of the immune system, and can be identified in vitro upon release from the controlling mechanisms that are likely to regulate them in vivo.
通过用佐剂乳化的抗原免疫小鼠来引发自身免疫反应的标准方法,会刺激强烈的辅助性(CD4)T细胞和抗体反应,但据报道不会诱导细胞毒性CD8 T细胞。本研究的目的是评估在用佐剂中的“弱”自身抗原免疫后,是否能轻易产生特异性自身反应性CD8 T细胞。用弗氏完全佐剂乳化的线粒体2-氧代酸脱氢酶复合物(二氢硫辛酰胺脱氢酶)的E3亚基对小鼠进行三次腹腔免疫。14天后收集脾和淋巴结淋巴细胞用于体外功能研究。检测T淋巴细胞对抗原负载的同基因靶细胞的增殖反应和细胞毒性。仅在用E3抗原负载的同基因脾细胞对淋巴细胞进行体外再刺激后,才能检测到自身反应性细胞溶解T淋巴细胞(CTL)反应。这些CTL被鉴定为H-2限制性CD8 + T细胞。对E3的增殖反应可针对抗原脉冲的同基因脾细胞表现出来。免疫小鼠也产生了对E3的强烈抗体反应。肝脏组织学显示门静脉浸润,被解释为肝脏对非特异性免疫刺激的反应。结论是,自身反应性细胞溶解T细胞可在适当刺激免疫系统后通过实验产生,并且在从可能在体内调节它们的控制机制中释放后可在体外鉴定出来。