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碳酸酐酶II是一种树突状细胞疗法靶向的肿瘤血管内皮相关抗原。

Carbonic anhydrase II is a tumor vessel endothelium-associated antigen targeted by dendritic cell therapy.

作者信息

Yoshiura Kenta, Nakaoka Takashi, Nishishita Toshihide, Sato Katsuaki, Yamamoto Akifumi, Shimada Shinji, Saida Toshiaki, Kawakami Yutaka, Takahashi Tsuneo A, Fukuda Hiroyuki, Imajoh-Ohmi Shinobu, Oyaizu Naoki, Yamashita Naohide

机构信息

Department of Advanced Medical Science, University of Tokyo, Japan.

出版信息

Clin Cancer Res. 2005 Nov 15;11(22):8201-7. doi: 10.1158/1078-0432.CCR-05-0816.

Abstract

Tumor-associated antigens are promising candidates as target molecules for immunotherapy and a wide variety of tumor-associated antigens have been discovered through the presence of serum antibodies in cancer patients. We previously conducted dendritic cell therapy on 10 malignant melanoma patients and shrinkage or disappearance of metastatic tumors with massive necrosis occurred in two patients. In this study, we found a 29-kDa protein against which antibody was elicited by dendritic cell therapy in one of the two patients. Matrix-assisted laser desorption ionization-time of flight/mass spectrometry analysis of the protein isolated by two-dimensional electrophoresis combined with Western blots revealed that the 29-kDa protein was carbonic anhydrase II (CA-II). Immunohistochemistry of the tumors and normal tissues showed that CA-II was expressed in the tumor vessel but not in normal vessel endothelium. CA-II expression in tumor endothelium was observed as well in other cancers including esophageal, renal, and lung cancers. In an in vitro angiogenesis model, CA-II expression of normal human vein endothelial cells was significantly up-regulated when cells were cultured in the acidic and hypoxic conditions indicative of a tumor environment. These findings suggest that CA-II is a tumor vessel endothelium-associated antigen in melanoma and other cancers, and elicitation of serum anti-CA-II antibody by dendritic cell therapy may be associated with good clinical outcome including tumor reduction.

摘要

肿瘤相关抗原作为免疫治疗的靶分子具有很大潜力,通过癌症患者血清抗体的存在已发现了多种肿瘤相关抗原。我们之前对10例恶性黑色素瘤患者进行了树突状细胞治疗,其中2例患者出现了伴有大量坏死的转移性肿瘤缩小或消失。在本研究中,我们在这2例患者中的1例发现了一种29 kDa的蛋白,树突状细胞治疗可诱导产生针对该蛋白的抗体。通过二维电泳结合蛋白质印迹法分离该蛋白后进行基质辅助激光解吸电离飞行时间质谱分析,结果显示该29 kDa蛋白为碳酸酐酶II(CA-II)。肿瘤和正常组织的免疫组织化学分析表明,CA-II在肿瘤血管中表达,但在正常血管内皮中不表达。在包括食管癌、肾癌和肺癌在内的其他癌症中也观察到肿瘤内皮中有CA-II表达。在体外血管生成模型中,当人正常静脉内皮细胞在模拟肿瘤环境的酸性和缺氧条件下培养时,CA-II的表达显著上调。这些发现表明,CA-II是黑色素瘤和其他癌症中与肿瘤血管内皮相关的抗原,树突状细胞治疗诱导血清抗CA-II抗体产生可能与包括肿瘤缩小在内的良好临床结果相关。

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