Vitale Marco, Pelusi Giuseppe, Taroni Beatrice, Gobbi Giuliana, Micheloni Cristina, Rezzani Rita, Donato Francesco, Wang Xinhui, Ferrone Soldano
Department of Anatomy, Pharmacology and Forensic Medicine, University of Parma, Italy.
Clin Cancer Res. 2005 Jan 1;11(1):67-72.
To investigate TAP1, TAP2, and HLA class I antigen expression in primary ovarian carcinoma lesions and to assess the clinical significance of defects in the expression of these molecules.
Fifty-one formalin-fixed, paraffin-embedded primary ovarian carcinoma lesions were stained with affinity-purified rabbit anti-TAP1 and anti-TAP2 antibodies and with anti-HLA class I heavy chain monoclonal antibody (mAb) HC-10 using the immunoperoxidase reaction. The results of immunohistochemical staining were correlated with the histopathologic characteristics of the lesions and with patients' survival.
Ovarian surface epithelium, thecal cells of follicles, and stromal cells were stained by anti-TAP1, anti-TAP2, and anti-HLA class I antigen xenoantibodies with a homogeneous pattern. In contrast, no staining of lutheinic cells by these antibodies was detected. Forty-one and 32 out of 51 primary ovarian carcinoma lesions were stained by anti-TAP1 and anti-TAP2 xenoantibodies and by anti-HLA class I antigen mAb HC-10, respectively. The staining patterns by anti-TAP1 and anti-TAP2 xenoantibodies were completely concordant, but did not correlate with that by anti-HLA class I heavy chain mAb HC-10. TAP1 and TAP2 expression was associated neither with the histopathologic characteristics of the lesions nor with clinical variables. On the other hand, HLA class I antigen down-regulation was associated with disease stage: the odds ratio of stage III for HLA class I antigen negative patients was 7.6 (95% confidence interval, 1.9-30.5; P= 0.007), whereas for TAP negative patients was 5.1 (95% confidence interval, 0.9-28.4; P = 0.07). Follow up was available for 39 out of the 51 patients. Multivariate analysis showed that both grading and staging were associated with a higher risk of death, whereas TAP and HLA class I antigen phenotypes were not.
The lack of association between TAP and HLA class I antigen expression is compatible with the possibility that multiple mechanisms underlie HLA class I antigen down-regulation in primary ovarian carcinoma lesions. The potential role of immunologic events in the clinical course of ovarian carcinoma suggests that the association between HLA class I antigen down-regulation and disease progression may reflect the escape of tumor cells from immune recognition and destruction.
研究原发性卵巢癌病变中TAP1、TAP2和HLA I类抗原的表达情况,并评估这些分子表达缺陷的临床意义。
采用免疫过氧化物酶反应,用亲和纯化的兔抗TAP1和抗TAP2抗体以及抗HLA I类重链单克隆抗体(mAb)HC - 10对51例福尔马林固定、石蜡包埋的原发性卵巢癌病变进行染色。免疫组织化学染色结果与病变的组织病理学特征及患者生存率相关。
抗TAP1、抗TAP2和抗HLA I类抗原异种抗体对卵巢表面上皮、卵泡膜细胞和基质细胞进行均匀染色。相比之下,未检测到这些抗体对黄体细胞的染色。51例原发性卵巢癌病变中,分别有41例和32例被抗TAP1和抗TAP2异种抗体以及抗HLA I类抗原mAb HC - 10染色。抗TAP1和抗TAP2异种抗体的染色模式完全一致,但与抗HLA I类重链mAb HC - 10的染色模式不相关。TAP1和TAP2的表达既与病变的组织病理学特征无关,也与临床变量无关。另一方面,HLA I类抗原下调与疾病分期相关:HLA I类抗原阴性患者III期的优势比为7.6(95%置信区间,1.9 - 30.5;P = 0.007),而TAP阴性患者为5.1(95%置信区间,0.9 - 28.4;P = 0.07)。51例患者中有39例进行了随访。多因素分析表明,分级和分期均与较高的死亡风险相关,而TAP和HLA I类抗原表型则不然。
TAP与HLA I类抗原表达之间缺乏相关性,这与原发性卵巢癌病变中HLA I类抗原下调存在多种机制的可能性相符。免疫事件在卵巢癌临床病程中的潜在作用表明,HLA I类抗原下调与疾病进展之间的关联可能反映了肿瘤细胞逃避免疫识别和破坏。