• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用荷癌患者的淋巴因子激活的杀伤细胞(LAK细胞),双特异性抗体OH1增强对癌胚抗原(CEA)阳性细胞系的细胞毒性作用。

Potentiation of cytotoxicity against a CEA positive cell line by the bispecific antibody OH1 using LAK cells from cancer-bearing patients.

作者信息

Baba M, Hideshima T, Yamashita Y, Shirakusa T

机构信息

Second Department of Surgery, School of Medicine, Fukuoka University, Fukuoka 814-0180, Japan.

出版信息

Oncol Rep. 1998 Sep-Oct;5(5):1141-6. doi: 10.3892/or.5.5.1141.

DOI:10.3892/or.5.5.1141
PMID:9683825
Abstract

Bispecific antibody, OH1 was developed, which simultaneously recognizes CD3 on T cells and carcinoembryonic antigen (CEA) on tumor cells. Although there was not significant difference, PBMCs pretreated with OH1 showed tendency to prolong survival of KATO III-injected SCID mice compared with control groups. although cytotoxicity of LAK cells from cancer-bearing patients was suppressed compared with that of cells of healthy donors, LAK cells from the patients pretreated with OH1 showed significantly increased cytotoxicity against KATO III cells. These results suggest that OH1 could be useful in immunotherapy with LAK cells for carcinomas that express CEA on the membrane.

摘要

双特异性抗体OH1被研发出来,它能同时识别T细胞上的CD3和肿瘤细胞上的癌胚抗原(CEA)。尽管没有显著差异,但与对照组相比,用OH1预处理的外周血单核细胞(PBMCs)显示出延长接种KATO III的SCID小鼠生存期的趋势。尽管荷癌患者的淋巴因子激活的杀伤细胞(LAK细胞)的细胞毒性与健康供体的细胞相比受到抑制,但用OH1预处理的患者的LAK细胞对KATO III细胞的细胞毒性显著增加。这些结果表明,OH1可用于对膜上表达CEA的癌症进行LAK细胞免疫治疗。

相似文献

1
Potentiation of cytotoxicity against a CEA positive cell line by the bispecific antibody OH1 using LAK cells from cancer-bearing patients.使用荷癌患者的淋巴因子激活的杀伤细胞(LAK细胞),双特异性抗体OH1增强对癌胚抗原(CEA)阳性细胞系的细胞毒性作用。
Oncol Rep. 1998 Sep-Oct;5(5):1141-6. doi: 10.3892/or.5.5.1141.
2
The induction of cytotoxicity by a bispecific antibody against CEA positive cell line, in vitro.一种针对癌胚抗原(CEA)阳性细胞系的双特异性抗体在体外诱导细胞毒性作用。
Surg Today. 1996;26(2):83-8. doi: 10.1007/BF00311769.
3
Tumor growth suppression by a mouse/human chimeric anti-CEA antibody and lymphokine-activated killer cells in vitro and in SCID mouse xenograft model.小鼠/人嵌合抗癌胚抗原抗体及淋巴因子激活的杀伤细胞在体外和SCID小鼠异种移植模型中对肿瘤生长的抑制作用
Anticancer Res. 1998 Jan-Feb;18(1A):17-24.
4
MUC1-specific targeting immunotherapy with bispecific antibodies: inhibition of xenografted human bile duct carcinoma growth.双特异性抗体介导的MUC1特异性靶向免疫疗法:对异种移植人胆管癌生长的抑制作用
Cancer Res. 1996 Sep 15;56(18):4205-12.
5
A highly effective and stable bispecific diabody for cancer immunotherapy: cure of xenografted tumors by bispecific diabody and T-LAK cells.一种用于癌症免疫治疗的高效稳定双特异性双抗体:双特异性双抗体与T-LAK细胞治愈异种移植肿瘤
Cancer Immunol Immunother. 2004 Jun;53(6):497-509. doi: 10.1007/s00262-003-0465-9. Epub 2003 Nov 25.
6
Targeting of human breast cancer by a bispecific antibody directed against two tumour-associated antigens: ErbB-2 and carcinoembryonic antigen.一种针对两种肿瘤相关抗原(表皮生长因子受体-2和癌胚抗原)的双特异性抗体对人乳腺癌的靶向作用
Tumour Biol. 2002 Nov-Dec;23(6):337-47. doi: 10.1159/000069793.
7
Novel system for generating cytotoxic effector lymphocytes using carcinoembryonic antigen (CEA) peptide and cultured dendritic cells.使用癌胚抗原(CEA)肽和培养的树突状细胞生成细胞毒性效应淋巴细胞的新型系统。
Anticancer Res. 2002 Sep-Oct;22(5):2597-606.
8
Cytotoxicity of cytokine-induced killer cells coated with bispecific antibody against acute myeloid leukemia cells.双特异性抗体包被的细胞因子诱导杀伤细胞对急性髓系白血病细胞的细胞毒性。
Leuk Lymphoma. 1994 Jul;14(3-4):219-29. doi: 10.3109/10428199409049672.
9
Generation of dual specific bivalent BiTEs (dbBIspecific T-cell engaging antibodies) for cellular immunotherapy.用于细胞免疫疗法的双特异性二价 BiTE (双特异性 T 细胞衔接抗体)的产生。
BMC Cancer. 2019 Sep 5;19(1):882. doi: 10.1186/s12885-019-6056-8.
10
In vivo activation and expansion of T cells by a bi-specific antibody abolishes metastasis formation of human melanoma cells in SCID mice.
Int J Cancer. 1998 Mar 16;75(6):908-18. doi: 10.1002/(sici)1097-0215(19980316)75:6<908::aid-ijc14>3.0.co;2-z.