Millrain M, Chandler P, Dazzi F, Scott D, Simpson E, Dyson P J
Transplantation Biology Group, Medical Research Council Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, Du Cane Road, London W12 0NN, United Kingdom.
J Immunol. 2001 Oct 1;167(7):3756-64. doi: 10.4049/jimmunol.167.7.3756.
We have applied MHC class I tetramers representing the two H2(b) MHC class I-restricted epitopes of the mouse male-specific minor transplantation Ag, HY, to directly determine the extent of expansion and immunodominance within the CD8+ T cell compartment following exposure to male tissue. Immunization with male bone marrow (BM), spleen, dendritic cells (DCs) and by skin graft led to rapid expansion of both specificities occupying up to >20% of the CD8+ T cell pool. At a high dose, whole BM or spleen were found to be more effective at stimulating the response than BM-derived DCs. In vivo, immunodominance within the responding cell population was only observed following chronic Ag stimulation, whereas epitope immunodominance was established rapidly following in vitro restimulation. Peptide affinity for the restricting MHC molecule was greater for the immunodominant epitope, suggesting that this might be a factor in the emergence of immunodominance. Using tetramers, we were able to directly visualize the cross-primed CD8+ HY response, but we did not find it to be the principal route for MHC class I presentation. Immunization with female spleen or DCs coated with the full complement of defined HY peptides, including the A(b)-restricted CD4+ Th cell determinant, failed to induce tetramer-reactive cells.
我们应用了代表小鼠雄性特异性次要移植抗原HY的两种H2(b) MHC I类限制性表位的MHC I类四聚体,以直接确定暴露于雄性组织后CD8+ T细胞区内的扩增程度和免疫显性。用雄性骨髓(BM)、脾脏、树突状细胞(DC)免疫以及进行皮肤移植,导致两种特异性迅速扩增,在CD8+ T细胞库中所占比例高达>20%。高剂量时,发现全骨髓或脾脏比BM来源的DC更有效地刺激反应。在体内,仅在慢性抗原刺激后才观察到反应细胞群体内的免疫显性,而体外再刺激后表位免疫显性迅速确立。免疫显性表位与限制性MHC分子的肽亲和力更高,表明这可能是免疫显性出现的一个因素。使用四聚体,我们能够直接观察到交叉致敏的CD8+ HY反应,但我们没有发现它是MHC I类呈递的主要途径。用包被有完整定义的HY肽(包括A(b)限制性CD4+ Th细胞决定簇)的雌性脾脏或DC免疫,未能诱导出四聚体反应性细胞。