Spiotto Michael T, Yu Ping, Rowley Donald A, Nishimura Michael I, Meredith Stephen C, Gajewski Thomas F, Fu Yang Xin, Schreiber Hans
Department of Pathology, The University of Chicago, Chicago, IL 60637, USA.
Immunity. 2002 Dec;17(6):737-47. doi: 10.1016/s1074-7613(02)00480-6.
To explain why solid cancers grow or are rejected, we examined how the tumor stroma affected the level of antigen expression necessary to induce an immune response. We applied a tamoxifen-regulated Cre-loxP system to induce a model SIYRYYGL antigen recognized by the 2C T cell receptor. Solid tumors expressing the antigen at lower levels grew, whereas solid tumors expressing antigen induced to 26-fold higher levels were rejected. In contrast, mice rejected cell suspensions expressing higher or lower levels of the antigen. The antigen was likely crosspresented because draining lymph node responses required bone marrow-derived cells in the tumor stroma. Thus, tumor antigens expressed at levels sufficient for crosspresentation by bone marrow-derived stromal cells may overcome immunological "ignorance" to solid tumors.
为了解释实体癌为何生长或被排斥,我们研究了肿瘤基质如何影响诱导免疫反应所需的抗原表达水平。我们应用了他莫昔芬调节的Cre-loxP系统来诱导一种可被2C T细胞受体识别的模型SIYRYYGL抗原。低水平表达该抗原的实体瘤生长,而诱导表达水平提高26倍的实体瘤则被排斥。相比之下,小鼠排斥表达高水平或低水平抗原的细胞悬液。该抗原可能是通过交叉呈递的,因为引流淋巴结反应需要肿瘤基质中的骨髓来源细胞。因此,由骨髓来源的基质细胞以足以进行交叉呈递的水平表达的肿瘤抗原可能会克服对实体瘤的免疫“忽视”。