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白细胞介素-2基因转染肿瘤疫苗联合白细胞介素-6基因转染肿瘤疫苗的抗肿瘤作用

[Antitumor effect of interleukin-2 gene-transfected tumor vaccine in combination with interleukin-6 gene-transfected tumor vaccine].

作者信息

Cao X, Zhang W, Tao Q

机构信息

Department of Immunology, Second Military Medical University, Shanghai.

出版信息

Zhonghua Yi Xue Za Zhi. 1995 Oct;75(10):602-5, 639.

PMID:8697075
Abstract

It has been shown that IL-2 and IL-6 can cooperate to induce immune responses more effectively. In order to increase the therapeutic efficacy of cytokine gene-transfected tumor vaccines, we treated the experimental pulmonary metastatic melanoma-bearing mice with IL-2 gene-transfected tumor vaccine and IL-6 gene-transfected tumor vaccine. After the combined treatment, the pulmonary metastases were reduced more significantly and the survival time of tumor-bearing mice was also prolonged more significantly. The CTL activity, NK activity and IL-2-induced LAK activity, IL-2 and TNF secretion from the splenocytes of the above tumor-bearing mice increased more significantly than that of tumor-bearing mice treated with IL-2 gene-transfected vaccine or IL-6 gene-transfected vaccine alone. These results demonstrated that the combined use of IL-2 gene-transfected tumor vaccine and IL-6 gene-transfected tumor vaccine could achieve more potent antitumor effect via more efficient activation of immune functions. The experiment outlines a novel approach to the cytokine gene therapy of cancer.

摘要

已表明白细胞介素-2(IL-2)和白细胞介素-6(IL-6)可协同作用更有效地诱导免疫反应。为提高细胞因子基因转染肿瘤疫苗的治疗效果,我们用IL-2基因转染肿瘤疫苗和IL-6基因转染肿瘤疫苗处理实验性肺转移黑色素瘤荷瘤小鼠。联合治疗后,肺转移明显减少,荷瘤小鼠的生存时间也显著延长。上述荷瘤小鼠脾细胞的细胞毒性T淋巴细胞(CTL)活性、自然杀伤(NK)活性以及IL-2诱导的淋巴因子激活的杀伤细胞(LAK)活性、IL-2和肿瘤坏死因子(TNF)分泌比单独用IL-2基因转染疫苗或IL-6基因转染疫苗处理的荷瘤小鼠增加更显著。这些结果表明,联合使用IL-2基因转染肿瘤疫苗和IL-6基因转染肿瘤疫苗可通过更有效地激活免疫功能实现更强的抗肿瘤作用。该实验概述了一种癌症细胞因子基因治疗的新方法。

相似文献

1
[Antitumor effect of interleukin-2 gene-transfected tumor vaccine in combination with interleukin-6 gene-transfected tumor vaccine].白细胞介素-2基因转染肿瘤疫苗联合白细胞介素-6基因转染肿瘤疫苗的抗肿瘤作用
Zhonghua Yi Xue Za Zhi. 1995 Oct;75(10):602-5, 639.
2
Enhanced efficacy of combination of IL-2 gene and IL-6 gene-transfected tumor cells in the treatment of established metastatic tumors.白细胞介素-2基因与白细胞介素-6基因转染肿瘤细胞联合应用治疗已形成的转移性肿瘤的疗效增强
Gene Ther. 1996 May;3(5):421-6.
3
Enhanced antitumor immune responses of IL-2 gene-modified tumor vaccine by combination with IL-1 and low dose cyclophosphamide.白细胞介素-2基因修饰的肿瘤疫苗与白细胞介素-1及低剂量环磷酰胺联合应用增强抗肿瘤免疫反应
J Exp Clin Cancer Res. 1999 Jun;18(2):173-9.
4
Efficient inducation of local and systemic antitumor immune response by liposome-mediated intratumoral co-transfer of interleukin-2 gene and interleukin-6 gene.脂质体介导的白细胞介素-2基因和白细胞介素-6基因瘤内共转染对局部和全身抗肿瘤免疫反应的有效诱导
J Exp Clin Cancer Res. 1999 Jun;18(2):191-200.
5
Combined vaccination with major histocompatibility class I and interleukin 2 gene-transduced melanoma cells synergizes the cure of postsurgical established lung metastases.主要组织相容性复合体I类和白细胞介素2基因转导的黑色素瘤细胞联合疫苗接种可协同治愈术后已形成的肺转移瘤。
Cancer Res. 1995 Nov 1;55(21):4941-9.
6
Induction of antitumor immunity by combined immunogene therapy using IL-2 and IL-12 in low antigenic Lewis lung carcinoma.在低抗原性的Lewis肺癌中使用白细胞介素-2和白细胞介素-12联合免疫基因疗法诱导抗肿瘤免疫
Cancer Gene Ther. 2000 Nov;7(11):1481-90. doi: 10.1038/sj.cgt.7700251.
7
Intratumoral IL-18 gene transfer improves therapeutic efficacy of antibody-targeted superantigen in established murine melanoma.肿瘤内白细胞介素-18基因转移可提高抗体靶向超抗原对已建立的小鼠黑色素瘤的治疗效果。
Gene Ther. 2001 Apr;8(7):542-50. doi: 10.1038/sj.gt.3301428.
8
Antitumor effect of interleukin 7 in combination with local hyperthermia in mice bearing B16a melanoma cells.白细胞介素7联合局部热疗对荷B16a黑色素瘤细胞小鼠的抗肿瘤作用。
Stem Cells. 1993 Sep;11(5):412-21. doi: 10.1002/stem.5530110508.
9
Eradication of melanoma pulmonary metastases by immunotherapy with tumor cells engineered to secrete interleukin-2 or gamma interferon.通过用经基因工程改造以分泌白细胞介素-2或γ干扰素的肿瘤细胞进行免疫疗法根除黑色素瘤肺转移灶。
Cancer Gene Ther. 1997 Jan-Feb;4(1):33-41.
10
Endogenous and adoptively transferred A-NK and T-LAK cells continuously accumulate within murine metastases up to 48 h after inoculation.内源性和过继转移的A-NK细胞及T-LAK细胞在接种后48小时内持续在小鼠转移灶中积聚。
In Vivo. 1999 May-Jun;13(3):199-204.