Tsukahara Tomohide, Kawaguchi Satoshi, Torigoe Toshihiko, Asanuma Hiroko, Nakazawa Emiri, Shimozawa Kumiko, Nabeta Yuki, Kimura Shigeharu, Kaya Mitsunori, Nagoya Satoshi, Wada Takuro, Yamashita Toshihiko, Sato Noriyuki
Department of Orthopaedic Surgery, Sapporo Medical University School of Medicine, South 1, West 16, Chuo-ku, Sapporo 060-8543, Japan.
Cancer Sci. 2006 Dec;97(12):1374-80. doi: 10.1111/j.1349-7006.2006.00317.x. Epub 2006 Sep 21.
With the goal of establishing efficacious peptide-based immunotherapy for patients with bone and soft tissue sarcomas, we previously identified the cytotoxic T lymphocyte-defined osteosarcoma antigenic gene Papillomavirus binding factor. The present study was designed to determine the status of HLA class I expression in osteosarcoma and other bone and soft tissue sarcomas. Seventy-four formalin-fixed paraffin-embedded specimens of various bone and soft tissue sarcomas, including 33 osteosarcomas, were stained with the anti-HLA class I monoclonal antibody EMR8-5, which we recently generated. The expression of HLA class I was lost or downregulated in 46 of these specimens (62%). With respect to osteosarcoma, loss or downregulation of HLA class I expression was seen in 13 (52%) of 25 primary tumors and seven (88%) of eight metastatic tumors. In six of 11 HLA class I-negative osteosarcoma specimens, the expression of beta-2 microglobulin was also lost. Subsequently the prognostic significance of HLA class I expression was analyzed in 21 patients with osteosarcoma who had completed multidrug neoadjuvant chemotherapy and undergone adequate surgery. Patients with osteosarcoma highly expressing HLA class I showed significantly better overall and event-free survival than those with HLA class I-negative osteosarcoma. In contrast, such prognostic significance of HLA class I expression was not found in 15 patients with malignant fibrous histiocytoma of soft tissue. These findings suggest that the class I-restricted cytotoxic T lymphocyte pathway plays a major role in immune surveillance of patients with osteosarcoma.
为了建立针对骨肉瘤和软组织肉瘤患者有效的基于肽的免疫疗法,我们之前鉴定出了细胞毒性T淋巴细胞定义的骨肉瘤抗原基因乳头瘤病毒结合因子。本研究旨在确定骨肉瘤以及其他骨和软组织肉瘤中HLA I类分子的表达状况。我们用最近制备的抗HLA I类单克隆抗体EMR8-5对74个不同骨和软组织肉瘤的福尔马林固定石蜡包埋标本进行染色,这些标本包括33个骨肉瘤。在这些标本中,有46个(62%)的HLA I类分子表达缺失或下调。就骨肉瘤而言,25个原发性肿瘤中有13个(52%)以及8个转移性肿瘤中有7个(88%)出现HLA I类分子表达缺失或下调。在11个HLA I类分子阴性的骨肉瘤标本中,有6个β2微球蛋白的表达也缺失。随后,我们对21例完成多药新辅助化疗并接受了充分手术的骨肉瘤患者分析了HLA I类分子表达的预后意义。HLA I类分子高表达的骨肉瘤患者的总生存率和无事件生存率显著高于HLA I类分子阴性的骨肉瘤患者。相比之下,在15例软组织恶性纤维组织细胞瘤患者中未发现HLA I类分子表达具有这样的预后意义。这些发现表明,I类分子限制的细胞毒性T淋巴细胞途径在骨肉瘤患者的免疫监视中起主要作用。