Suppr超能文献

Jaa-f11:延长患乳腺癌小鼠的寿命。

Jaa-f11: extending the life of mice with breast cancer.

作者信息

Rittenhouse-Olson Kate

机构信息

University at Buffalo, Department of Biotechnical and Clinical Laboratory Sciences, Buffalo, NY 14214, USA.

出版信息

Expert Opin Biol Ther. 2007 Jul;7(7):923-8. doi: 10.1517/14712598.7.7.923.

Abstract

JAA-F11 antibody (Ab) is a monoclonal Ab that is specific for the Thomsen-Friedenreich antigen, Galbeta1-3GalNAcalpha (TF-Ag). TF-Ag, discovered in the late 1920s, is a tumor-associated carbohydrate Ag of many clinically widespread carcinomas. In a mouse model, JAA-F11 Ab significantly extended median survival time of animals with metastatic 4T1 breast tumors and caused > 50% inhibition of lung metastasis. (124)Iodine labeled JAA-F11 Ab in in vivo micro positron emission tomography showed tumor specificity in a mouse breast tumor model, with no preferential uptake by any other organ. Human cancer cell adhesion to vascular endothelium was also blocked by JAA-F11. Structural specificity of the Ab was shown with glycan array analysis and indicated that this Ab, unlike many other Abs to TF-Ag, will not bind to a related glycolipid on natural killer cells, kidney or spleen. Patients with higher levels of naturally occurring anti-TF-Ag Ab appear to have a better prognosis, indicating that passive transfer of JAA-F11 or active immunization, resulting in production of anti-TF-Ag Ab, would clinically be beneficial for the patient.

摘要

JAA - F11抗体(Ab)是一种单克隆抗体,对桑德森 - 弗里德赖希抗原Galβ1 - 3GalNAcα(TF - Ag)具有特异性。TF - Ag于20世纪20年代末被发现,是许多临床常见癌症的肿瘤相关碳水化合物抗原。在小鼠模型中,JAA - F11抗体显著延长了转移性4T1乳腺肿瘤动物的中位生存时间,并导致> 50%的肺转移抑制。体内微型正电子发射断层扫描中用(124)碘标记的JAA - F11抗体在小鼠乳腺肿瘤模型中显示出肿瘤特异性,没有其他任何器官的优先摄取。JAA - F11还能阻断人癌细胞与血管内皮的黏附。聚糖阵列分析显示了该抗体的结构特异性,表明与许多其他针对TF - Ag的抗体不同,这种抗体不会与自然杀伤细胞、肾脏或脾脏上的相关糖脂结合。天然存在的抗TF - Ag抗体水平较高的患者似乎预后较好,这表明JAA - F11的被动转移或主动免疫导致抗TF - Ag抗体的产生在临床上对患者有益。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验