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[卵巢癌独特型疫苗免疫治疗试验。用单克隆抗体OC125治疗晚期卵巢癌患者激活独特型网络]

[A trial with immunotherapy of ovarian cancer by idiotype vaccination. Activation of the idiotype network in patients with advanced ovarian cancers by treatment with monoclonal antibody OC125].

作者信息

Wagner U, Reinsberg J, Krebs D

机构信息

Universitäts-Frauenklinik Bonn.

出版信息

Geburtshilfe Frauenheilkd. 1990 Oct;50(10):785-8. doi: 10.1055/s-2008-1026364.

DOI:10.1055/s-2008-1026364
PMID:2286317
Abstract

Up to date, the positive effect of immunotherapy, using tumour-associated antigens or tumour cells of ovarian carcinomas, is still vague. Another and effective approach to overcome an experimentally induced tolerance, is the presentation of an definitive antigen in a different surrounding by the induction of the idiotypic network. Antibodies against a tumour-associated antigen are used to induce following antibodies, which are directed against the variable antigen-binding group, the so-called idiotype of the antibody-vaccine. Then, the induced antibodies carry a mirror image of the tumour-associated antigen and are therefore able to modulate the host's immune response against the tumour. For the induction of this system, we used the monoclonal antibody OC125 as a F(ab)2-fragment, which is directed against the tumour-associated antigen CA125 of epithelial ovarian carcinomas. 12 patients with advanced ovarian carcinomas received antibody fragments of the OC125 in the course of radioimmunodetections since 1985. Until April 1990 only these 5 patients, who developed the anti-idiotypic antibodies after the vaccination, are still alive. Our first results with the induction of the idiotypic network system for patients with advanced ovarian carcinomas indicate, that in spite of the same surgical and chemotherapeutical treatment, patients show a delayed clinical course after the induction of the idiotypic system. The transfer of the definitive tumour-associated antigen in an idiotypic antigen, seems to modulate the immunoresponse of the patients and in this way also the clinical course of a malignancy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

迄今为止,使用卵巢癌肿瘤相关抗原或肿瘤细胞进行免疫治疗的积极效果仍不明确。另一种克服实验性诱导耐受性的有效方法是通过独特型网络的诱导,在不同环境中呈现确定的抗原。针对肿瘤相关抗原的抗体用于诱导后续抗体,这些抗体针对可变抗原结合基团,即所谓的抗体疫苗独特型。然后,诱导产生的抗体携带肿瘤相关抗原的镜像,因此能够调节宿主针对肿瘤的免疫反应。为了诱导这个系统,我们使用单克隆抗体OC125作为F(ab)2片段,它针对上皮性卵巢癌的肿瘤相关抗原CA125。自1985年以来,12例晚期卵巢癌患者在放射免疫检测过程中接受了OC125的抗体片段。直到1990年4月,只有这5例在接种疫苗后产生抗独特型抗体的患者仍然存活。我们对晚期卵巢癌患者诱导独特型网络系统的初步结果表明,尽管采用相同的手术和化疗治疗,但患者在诱导独特型系统后临床病程出现延迟。将确定的肿瘤相关抗原转化为独特型抗原,似乎调节了患者的免疫反应,进而也调节了恶性肿瘤的临床病程。(摘要截短至250字)

相似文献

1
[A trial with immunotherapy of ovarian cancer by idiotype vaccination. Activation of the idiotype network in patients with advanced ovarian cancers by treatment with monoclonal antibody OC125].[卵巢癌独特型疫苗免疫治疗试验。用单克隆抗体OC125治疗晚期卵巢癌患者激活独特型网络]
Geburtshilfe Frauenheilkd. 1990 Oct;50(10):785-8. doi: 10.1055/s-2008-1026364.
2
[Monoclonal anti-idiotype antibodies in immunotherapy of ovarian carcinoma (MAb ACA125) and breast carcinoma (MAb ACA14C5)].[单克隆抗独特型抗体在卵巢癌(单克隆抗体ACA125)和乳腺癌(单克隆抗体ACA14C5)免疫治疗中的应用]
Zentralbl Gynakol. 1999;121(4):190-5.
3
Immunotherapy of advanced ovarian carcinomas by activation of the idiotypic network.通过激活独特型网络对晚期卵巢癌进行免疫治疗。
Biotechnol Ther. 1992;3(1-2):81-9.
4
Human antibody response to the intravenous and intraperitoneal administration of the F(ab')2 fragment of the OC125 murine monoclonal antibody.人类对OC125鼠单克隆抗体F(ab')2片段静脉内和腹腔内给药的抗体反应。
J Immunother (1991). 1992 Jan;11(1):56-66. doi: 10.1097/00002371-199201000-00007.
5
Immunological consolidation of ovarian carcinoma recurrences with monoclonal anti-idiotype antibody ACA125: immune responses and survival in palliative treatment. See The biology behind: K. A. Foon and M. Bhattacharya-Chatterjee, Are solid tumor anti-idiotype vaccines ready for prime time? Clin. Cancer Res., 7:1112-1115, 2001.用单克隆抗独特型抗体ACA125对复发性卵巢癌进行免疫巩固治疗:姑息治疗中的免疫反应和生存情况。见背后的生物学原理:K. A. 富恩和M. 巴塔查里亚 - 查特吉,实体瘤抗独特型疫苗准备好进入黄金时代了吗?《临床癌症研究》,2001年,第7卷,第1112 - 1115页 。
Clin Cancer Res. 2001 May;7(5):1154-62.
6
[Immune reactions and survival of patients with ovarian carcinomas after administration of 131I-F(Ab)2 fragments of the OC 125 monoclonal antibody].
Geburtshilfe Frauenheilkd. 1995 Apr;55(4):200-3. doi: 10.1055/s-2007-1023301.
7
Idiotypic cascades after MAb OC125 application.
Hybridoma. 1993 Oct;12(5):577-82. doi: 10.1089/hyb.1993.12.577.
8
Interleukin-6 fused to an anti-idiotype antibody in a vaccine increases the specific humoral immune response against CA125+ (MUC-16) ovarian cancer.在疫苗中与抗独特型抗体融合的白细胞介素-6可增强针对CA125+(MUC-16)卵巢癌的特异性体液免疫反应。
Cancer Res. 2003 Jun 15;63(12):3234-40.
9
Cytotoxic effects of T cells induced by fusion protein 6B11-pulsed dendritic cells on ovarian carcinoma cells.融合蛋白6B11脉冲树突状细胞诱导的T细胞对卵巢癌细胞的细胞毒性作用。
Gynecol Oncol. 2007 Apr;105(1):238-43. doi: 10.1016/j.ygyno.2006.04.028.
10
Generation of monoclonal antibodies utilizing the host anti-idiotypic network.利用宿主抗独特型网络产生单克隆抗体。
In Vivo. 1995 Mar-Apr;9(2):139-44.

引用本文的文献

1
False changes in CA 125 levels in ovarian cancer patients after infusion of OC125 fragments for diagnostic and therapeutic purpose.为诊断和治疗目的输注OC125片段后,卵巢癌患者CA 125水平出现假性变化。
Arch Gynecol Obstet. 1994;255(1):9-18. doi: 10.1007/BF02390669.