Chen H L, Gabrilovich D, Tampé R, Girgis K R, Nadaf S, Carbone D P
Harmon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas 75235-8593, USA.
Nat Genet. 1996 Jun;13(2):210-3. doi: 10.1038/ng0696-210.
Tumours express a variety of novel epitopes which represent potential immune targets, and thus clinically evident tumours are thought to have effectively avoided immune recognition and elimination. Transporters associated with antigen presentation (TAP) are thought to be responsible for conveying intracellular peptides into the endoplasmic reticulum for complex formation with class I MHC and subsequent recognition by cytotoxic T lymphocytes. In this study, we evaluated 79 human solid tumours and cell lines for genetic abnormalities in TAP1 that might have led to an acquired loss of antigen presenting ability. A novel sequence (R659Q) was discovered near the ATP binding site in a human small cell lung cancer (SCLC) cell line, H1436. This cell line is heterozygous for this allele, but only the R659Q allele is transcribed into RNA. Even though the R659Q protein is expressed, these cells act as if they were TAP deficient by peptide binding and antigen presentation studies, which are restored after transfection of a functional TAP1 allele. This is the first evidence for a naturally occuring protein structural defect resulting in defective peptide transport in a human solid tumour.
肿瘤表达多种新型表位,这些表位代表潜在的免疫靶点,因此临床上可见的肿瘤被认为有效地避免了免疫识别和清除。与抗原呈递相关的转运蛋白(TAP)被认为负责将细胞内肽转运至内质网,以便与I类主要组织相容性复合体(MHC)形成复合物,并随后被细胞毒性T淋巴细胞识别。在本研究中,我们评估了79个人类实体瘤和细胞系中TAP1的基因异常情况,这些异常可能导致抗原呈递能力的后天丧失。在人小细胞肺癌(SCLC)细胞系H1436的ATP结合位点附近发现了一个新序列(R659Q)。该细胞系对于这个等位基因是杂合的,但只有R659Q等位基因被转录为RNA。尽管表达了R659Q蛋白,但通过肽结合和抗原呈递研究,这些细胞的行为就好像它们缺乏TAP一样,在转染功能性TAP1等位基因后得以恢复。这是人类实体瘤中自然发生的蛋白质结构缺陷导致肽转运缺陷的首个证据。