Doménech N, Henderson R A, Finn O J
Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, PA 15261, USA.
J Immunol. 1995 Nov 15;155(10):4766-74.
Epithelial cell mucin encoded by the MUC-1 gene is overexpressed and aberrantly glycosylated on pancreatic, breast, and ovarian cancers as well as on multiple myelomas. It is recognized by patients' Ab and by T cells derived from tumor-draining lymph nodes. The T cell recognition is not MHC restricted and is specific for an epitope previously localized to the immunodominant tandem repeat region of the native mucin molecule. In search of possible MHC-restricted epitopes in the same immunodominant region, we synthesized a panel of overlapping, nine-amino acid long peptides spanning the MUC-1 tandem repeat and first examined their binding to specific human MHC class I molecules using two independent flow cytometry-based assay systems. This approach identified one peptide, p9-17 (STAPPAHGV), that bound to HLA-A1, -A2.1, -A3, and -A11. Measurements of the affinity of binding to each of these alleles, using a quantitative molecular binding assay, indicated that only the relative binding affinity to HLA-A11 was close to immunogenic values. We tested the immunogenicity of p9-17 in vitro. We detected a secondary T cell response specific for p9-17 in lymph nodes from an HLA-A11 breast cancer patient. Moreover, CTL specific for p9-17 peptide could be generated from PBL in several healthy HLA-A11 donors by primary in vitro stimulation.
由MUC-1基因编码的上皮细胞粘蛋白在胰腺癌、乳腺癌、卵巢癌以及多发性骨髓瘤中过度表达且发生异常糖基化。它能被患者的抗体以及来自肿瘤引流淋巴结的T细胞识别。T细胞识别不受MHC限制,且对先前定位在天然粘蛋白分子免疫显性串联重复区域的一个表位具有特异性。为了在同一免疫显性区域寻找可能受MHC限制的表位,我们合成了一组覆盖MUC-1串联重复序列的重叠的九氨基酸长肽,并首先使用两种基于流式细胞术的独立检测系统检测它们与特定人类MHC I类分子的结合情况。这种方法鉴定出一种肽p9-17(STAPPAHGV),它能与HLA-A1、-A2.1、-A3和-A11结合。使用定量分子结合测定法测量与这些等位基因中每一个的结合亲和力,结果表明只有与HLA-A11的相对结合亲和力接近免疫原性值。我们在体外测试了p9-17的免疫原性。我们在一名HLA-A11乳腺癌患者的淋巴结中检测到了对p9-17特异的二次T细胞反应。此外,通过体外初次刺激,在几名健康的HLA-A11供体的外周血淋巴细胞中可以产生对p9-17肽特异的CTL。