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利用碳酸酐酶 IX-鲍曼不动杆菌外膜蛋白 A 融合蛋白脉冲树突状细胞产生抗肾细胞癌免疫反应。

Generation of anti-tumour immune response using dendritic cells pulsed with carbonic anhydrase IX-Acinetobacter baumannii outer membrane protein A fusion proteins against renal cell carcinoma.

机构信息

Department of Microbiology, Kyungpook National University School of Medicine, Daegu, Korea.

出版信息

Clin Exp Immunol. 2012 Jan;167(1):73-83. doi: 10.1111/j.1365-2249.2011.04489.x.

Abstract

Carbonic anhydrase IX (CA9), a specific molecular marker for renal cell carcinoma (RCC), serves as a potential target for RCC-specific immunotherapy using dendritic cells (DCs). However, pulsing of DCs with CA9 alone is not sufficient for generation of a therapeutic anti-tumour immune response against RCC. In this study, in order to generate a potent anti-tumour immune response against RCC, we produced recombinant CA9-Acinetobacter baumannii outer membrane protein A (AbOmpA) fusion proteins, designated CA9-AbOmpA, and investigated the ability of DCs pulsed with CA9-AbOmpA fusion proteins in a murine renal cell carcinoma (RENCA) model. A recombinant CA9-AbOmpA fusion protein was composed of a unique proteoglycan-related region of CA9 (1-120 amino acids) fused at the C-terminus with transmembrane domain of AbOmpA (1-200 amino acids). This fusion protein was capable of inducing DC maturation and interleukin (IL)-12 production in DCs. Interaction of DCs pulsed with CA9-AbOmpA fusion proteins with naive T cells stimulated secretion of IL-2, interferon (IFN)-γ and tumour necrosis factor (TNF)-α in T cells. Lymphocytes harvested from mice immunized with DCs pulsed with CA9-AbOmpA fusion proteins secreted IFN-γ and showed a specific cytotoxic activity against CA9-expressing RENCA (RENCA-CA9) cells. Administration of CA9-AbOmpA-pulsed DC vaccine suppressed growth of RENCA-CA9 cells in mice with an established tumour burden. These results suggest that DCs pulsed with CA9-AbOmpA fusion proteins generate a specific anti-tumour immune response against RCC, which can be utilized in immunotherapy of RCC.

摘要

碳酸酐酶 9(CA9)是肾细胞癌(RCC)的特定分子标志物,可作为使用树突状细胞(DC)进行 RCC 特异性免疫治疗的潜在靶标。然而,仅用 CA9 脉冲 DC 不足以产生针对 RCC 的治疗性抗肿瘤免疫反应。在这项研究中,为了产生针对 RCC 的有效抗肿瘤免疫反应,我们制备了重组 CA9-鲍曼不动杆菌外膜蛋白 A(AbOmpA)融合蛋白,命名为 CA9-AbOmpA,并在小鼠肾细胞癌(RENCA)模型中研究了用 CA9-AbOmpA 融合蛋白脉冲的 DC 的能力。重组 CA9-AbOmpA 融合蛋白由 CA9 的独特糖胺聚糖相关区域(1-120 个氨基酸)组成,其 C 末端融合有 AbOmpA 的跨膜结构域(1-200 个氨基酸)。该融合蛋白能够诱导 DC 成熟和白细胞介素(IL)-12 的产生。与 CA9-AbOmpA 融合蛋白脉冲的 DC 相互作用刺激幼稚 T 细胞分泌白细胞介素(IL)-2、干扰素(IFN)-γ 和肿瘤坏死因子(TNF)-α。用 CA9-AbOmpA 融合蛋白脉冲的 DC 免疫的小鼠中分离的淋巴细胞分泌 IFN-γ,并对表达 CA9 的 RENCA(RENCA-CA9)细胞显示出特异性细胞毒性活性。CA9-AbOmpA 脉冲的 DC 疫苗的给药抑制了具有既定肿瘤负担的小鼠中 RENCA-CA9 细胞的生长。这些结果表明,用 CA9-AbOmpA 融合蛋白脉冲的 DC 可产生针对 RCC 的特异性抗肿瘤免疫反应,可用于 RCC 的免疫治疗。

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