Trieb K, Lechleitner T, Lang S, Windhager R, Kotz R, Dirnhofer S
Department of Orthopaedics, University Hospital Vienna, Austria.
Pathol Res Pract. 1998;194(10):679-84. doi: 10.1016/S0344-0338(98)80126-X.
Although in recent years the outcome of patients with osteosarcoma has considerably been improved by combining neoadjuvant chemotherapy with radical surgery, there still remains the problem of nonresponse to chemotherapy. T-lymphocytes play a critical role in tumor immunology, and MHC molecules are of central importance in the regulation of the immune response. It is the aim of this study to investigate whether T-lymphocyte infiltration of osteosarcomas and HLA-DR expression on tumor cells and infiltrating immune cells are of predictive or diagnostic value. Expression of CD3, CD8 and HLA-II was evaluated immunohistochemically on paraffin-embedded sections of 35 patients with high-grade osteosarcoma at the time of biopsy before chemotherapy and correlated with histologic response to chemotherapy, tumor size, age, alkaline-phosphatase serum levels and duration of symptoms. Thirty-four patients with osteoblastoma (n = 7), osteoid osteoma (n = 7) or fibrous dysplasia (n = 20) served as controls. Osteosarcomas were infiltrated by CD3+ (33/35, 95%) and CD8+ T-lymphocytes (24/35, 68%), non malignant bone tumors by CD3+ in 91% (31/34) and CD8+ T-lymphocytes in 74% (25/34), respectively. T-lymphocytes were positive for HLA-DR expression in 29% (10/35) in osteosarcomas and in 11% (4/34) in non-malignant controls. Osteosarcoma cells were positive for HLA-DR in 11/35 (31%) and non-malignant tumor cells in only 9% (3/34). Therefore, HLA-DR is overexpressed in osteosarcoma (p < 0.05). HLA-DR expression on osteosarcoma cells showed a positive correlation with HLA-DR expression on lymphocytes (p < 0.001) as well as with duration of symptoms and age (p < 0.05). Response to preoperative chemotherapy, gender, tumor size and serum alkaline-phosphatase levels did not correlate with the expression of the molecules tested. Our results show that HLA-DR is overexpressed in osteosarcoma cells compared to non-malignant bone-tumors. This overexpression, however, fails to serve as a predictive marker for response to neoadjuvant chemotherapy. The same is also true for tumor-infiltrating lymphocytes expressing CD3, CD8 and HLA-DR. Increased HLA-DR expression in osteosarcoma is most likely due to the immune response against the tumor.
尽管近年来通过新辅助化疗与根治性手术相结合,骨肉瘤患者的治疗结果有了显著改善,但化疗无反应的问题仍然存在。T淋巴细胞在肿瘤免疫学中起关键作用,而MHC分子在免疫反应调节中至关重要。本研究的目的是调查骨肉瘤中T淋巴细胞浸润以及肿瘤细胞和浸润免疫细胞上HLA - DR表达是否具有预测或诊断价值。在35例高级别骨肉瘤患者化疗前活检时的石蜡包埋切片上,通过免疫组织化学评估CD3、CD8和HLA - II的表达,并将其与化疗的组织学反应、肿瘤大小、年龄、血清碱性磷酸酶水平和症状持续时间相关联。34例骨母细胞瘤(n = 7)、骨样骨瘤(n = 7)或骨纤维异常增殖症(n = 20)患者作为对照。骨肉瘤中CD3 +(33/35,95%)和CD8 + T淋巴细胞浸润(24/35,68%),非恶性骨肿瘤中CD3 +浸润率为91%(31/34),CD8 + T淋巴细胞浸润率为74%(25/34)。骨肉瘤中29%(10/35)的T淋巴细胞HLA - DR表达呈阳性,非恶性对照中为11%(4/34)。骨肉瘤细胞中11/35(31%)的HLA - DR呈阳性,非恶性肿瘤细胞中仅9%(3/34)呈阳性。因此,骨肉瘤中HLA - DR过度表达(p < 0.05)。骨肉瘤细胞上的HLA - DR表达与淋巴细胞上的HLA - DR表达呈正相关(p < 0.001),也与症状持续时间和年龄呈正相关(p < 0.05)。术前化疗反应、性别、肿瘤大小和血清碱性磷酸酶水平与所检测分子的表达无关。我们的结果表明,与非恶性骨肿瘤相比,骨肉瘤细胞中HLA - DR过度表达。然而,这种过度表达不能作为新辅助化疗反应的预测标志物。对于表达CD3、CD8和HLA - DR的肿瘤浸润淋巴细胞也是如此。骨肉瘤中HLA - DR表达增加很可能是由于针对肿瘤的免疫反应。