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重组MUC 1痘苗病毒:一种用于乳腺癌免疫治疗的潜在载体。

Recombinant MUC 1 vaccinia virus: a potential vector for immunotherapy of breast cancer.

作者信息

Balloul J M, Acres R B, Geist M, Dott K, Stefani L, Schmitt D, Drillien R, Spehner D, McKenzie I, Xing P X

机构信息

INSERM U74, Université Louis Pasteur, Strasbourg, France.

出版信息

Cell Mol Biol (Noisy-le-grand). 1994;40 Suppl 1:49-59.

PMID:7950862
Abstract

Breast cancer is considered as the major cause of mortality by cancer for women. Even if chemotherapy, radiotherapy and surgery have improved the life expectancy of patients bearing tumours, breast cancer is responsible for the death of 42,000 women per year in USA and 25,000 women in France. In this context, cancer vaccines may add an attractive alternative therapeutic strategy to the current existing treatments. We describe here the construction of recombinant vaccinia viruses co-expressing a tumour associated antigen (MUC 1) and an "adjuvant" cytokine, which have potential applications in the active immunotherapy of breast cancer. Indeed, recombinant vaccinia viruses have been extensively used during the past decade to induce a protective response against a whole variety of pathogens, and has proven to be of great value in the elicitation of a cellular immune response leading to the rejection of tumour grafts in mouse models.

摘要

乳腺癌被认为是女性癌症死亡的主要原因。即使化疗、放疗和手术提高了患肿瘤患者的预期寿命,但在美国每年仍有42000名女性因乳腺癌死亡,在法国这一数字为25000名。在此背景下,癌症疫苗可能为现有治疗方法增添一种有吸引力的替代治疗策略。我们在此描述了共表达肿瘤相关抗原(MUC 1)和“佐剂”细胞因子的重组痘苗病毒的构建,其在乳腺癌的主动免疫治疗中具有潜在应用。事实上,在过去十年中,重组痘苗病毒已被广泛用于诱导针对各种病原体的保护性反应,并且已证明在引发细胞免疫反应以导致小鼠模型中的肿瘤移植物排斥方面具有巨大价值。

相似文献

1
Recombinant MUC 1 vaccinia virus: a potential vector for immunotherapy of breast cancer.重组MUC 1痘苗病毒:一种用于乳腺癌免疫治疗的潜在载体。
Cell Mol Biol (Noisy-le-grand). 1994;40 Suppl 1:49-59.
2
Prospects and limitations of recombinant poxviruses for prostate cancer immunotherapy.重组痘病毒用于前列腺癌免疫治疗的前景与局限性
Curr Opin Mol Ther. 1999 Aug;1(4):471-9.
3
Does pregnancy immunize against breast cancer?
Cancer Res. 1995 Jun 1;55(11):2257-61.
4
Technology evaluation: TG-1031, Transgene SA.技术评估:TG-1031,转基因公司。
Curr Opin Mol Ther. 2000 Feb;2(1):106-11.
5
Breast cancer associated mucin: a review.乳腺癌相关黏蛋白:综述
Allergol Immunopathol (Madr). 1997 Jul-Aug;25(4):176-81.
6
In situ cytokine gene transfection using vaccinia virus vectors.使用痘苗病毒载体进行原位细胞因子基因转染。
Semin Oncol. 1996 Feb;23(1):88-100.
7
Intramuscular immunization with plasmid coexpressing tumour antigen and Flt-3L results in potent tumour regression.用共表达肿瘤抗原和Flt-3L的质粒进行肌肉内免疫可导致有效的肿瘤消退。
Gene Ther. 2006 Feb;13(3):245-56. doi: 10.1038/sj.gt.3302639.
8
Induction of protective host immunity to carcinoembryonic antigen (CEA), a self-antigen in CEA transgenic mice, by immunizing with a recombinant vaccinia-CEA virus.通过用重组痘苗-癌胚抗原(CEA)病毒免疫,在CEA转基因小鼠中诱导对癌胚抗原(CEA)这种自身抗原的保护性宿主免疫。
Cancer Res. 1999 Feb 1;59(3):676-83.
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Enhancement of vaccinia vaccine potency by linkage of tumor antigen gene to gene encoding calreticulin.通过将肿瘤抗原基因与编码钙网蛋白的基因连接来增强痘苗疫苗效力。
Vaccine. 2004 Sep 28;22(29-30):3993-4001. doi: 10.1016/j.vaccine.2004.03.057.
10
Recombinant DNA vaccines protect against tumors that are resistant to recombinant vaccinia vaccines containing the same gene.重组DNA疫苗可预防对含有相同基因的重组痘苗疫苗产生抗性的肿瘤。
Gene Ther. 2001 Jan;8(2):128-38. doi: 10.1038/sj.gt.3301370.

引用本文的文献

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Antitumor activity and immunogenicity of recombinant vaccinia virus expressing HPV 16 E7 protein SigE7LAMP is enhanced by high-level coexpression of IGFBP-3.表达人乳头瘤病毒16 E7蛋白的重组痘苗病毒SigE7LAMP的抗肿瘤活性和免疫原性通过胰岛素样生长因子结合蛋白-3的高水平共表达得到增强。
Cancer Gene Ther. 2014 Mar;21(3):115-25. doi: 10.1038/cgt.2014.6. Epub 2014 Feb 21.
2
Vaccinia viruses with mutations in the E3L gene as potential replication-competent, attenuated vaccines: intra-nasal vaccination.E3L基因发生突变的痘苗病毒作为具有潜在复制能力的减毒疫苗:鼻内接种。
Vaccine. 2008 Jan 30;26(5):664-76. doi: 10.1016/j.vaccine.2007.11.045. Epub 2007 Dec 4.
3
Poxvirus-based vaccine therapy for patients with advanced pancreatic cancer.
基于痘病毒的晚期胰腺癌患者疫苗疗法。
J Transl Med. 2007 Nov 26;5:60. doi: 10.1186/1479-5876-5-60.
4
Prospects for the therapeutic use of anticancer vaccines.抗癌疫苗的治疗应用前景。
Drugs. 1999 Mar;57(3):309-25. doi: 10.2165/00003495-199957030-00004.