Franco A, Tilly D A, Gramaglia I, Croft M, Cipolla L, Meldal M, Grey H M
Division of Immunochemistry, La Jolla Institute for Allergy and Immunology, San Diego, CA 92121, USA.
Nat Immunol. 2000 Aug;1(2):145-50. doi: 10.1038/77827.
We show here that priming and memory generation of antigen-specific CD8+ cytotoxic T lymphocytes (CTL) does not require help if the immunogen binds major histocompatibility complex (MHC) class I molecules with high affinity. This conclusion was based on the study of three chemically distinct optimal length CTL epitopes with high affinity for the restriction element Kb. In contrast, when two subdominant epitopes with intermediate MHC binding affinity were studied, either a class II MHC-restricted T helper cell epitope or administration of antibody to CD40 was required to obtain significant CTL priming. Depending on the epitope, one source of help was much more efficient than the other.
我们在此表明,如果免疫原与主要组织相容性复合体(MHC)I类分子高亲和力结合,抗原特异性CD8 + 细胞毒性T淋巴细胞(CTL)的启动和记忆生成不需要辅助。这一结论基于对三种化学性质不同、对限制性元件Kb具有高亲和力的最佳长度CTL表位的研究。相比之下,当研究两个具有中等MHC结合亲和力的次优势表位时,需要II类MHC限制性T辅助细胞表位或给予抗CD40抗体才能获得显著的CTL启动。根据表位的不同,一种辅助来源比另一种更有效。